Scholarly article on topic 'Cystic fibrosis: An inherited disease affecting mucin-producing organs'

Cystic fibrosis: An inherited disease affecting mucin-producing organs Academic research paper on "Biological sciences"

Share paper
{Mucin / Mucus / CF / CFTR / Pathogenesis}

Abstract of research paper on Biological sciences, author of scientific article — Camille Ehre, Caroline Ridley, David J. Thornton

Abstract Our current understanding of cystic fibrosis (CF) has revealed that the biophysical properties of mucus play a considerable role in the pathogenesis of the disease in view of the fact that most mucus-producing organs are affected in CF patients. In this review, we discuss the potential causal relationship between altered cystic fibrosis transmembrane conductance regulator (CFTR) function and the production of mucus with abnormal biophysical properties in the intestine and lungs, highlighting what has been learned from cell cultures and animal models that mimic CF pathogenesis. A similar cascade of events, including mucus obstruction, infection and inflammation, is common to all epithelia affected by impaired surface hydration. Hence, the main structural components of mucus, namely the polymeric, gel-forming mucins, are critical to the onset of the disease. Defective CFTR leads to epithelial surface dehydration, altered pH/electrolyte composition and mucin concentration. Further, it can influence mucin transition from the intracellular to extracellular environment, potentially resulting in aberrant mucus gel formation. While defective HCO3 − production has long been identified as a feature of CF, it has only recently been considered as a key player in the transition phase of mucins. We conclude by examining the influence of mucins on the biophysical properties of CF sputum and discuss existing and novel therapies aimed at removing mucus from the lungs. This article is part of a Directed Issue entitled: Cystic Fibrosis: From o-mics to cell biology, physiology, and therapeutic advances.

Academic research paper on topic "Cystic fibrosis: An inherited disease affecting mucin-producing organs"


The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx


Contents lists available at ScienceDirect

The International Journal of Biochemistry & Cell Biology

journal homepage


Cystic fibrosis: An inherited disease affecting mucin-producing organs

qi Camille Ehre3'*, Caroline Ridley b, David J. Thorntonb

a CF/Pulmonary Research & Treatment Centre, The University of North Carolina at Chapel Hill, USA b Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University ofManchester, UK

10 11 12


Article history:

Received 15 January 2014

Received in revised form 28 February 2014

Accepted 17 March 2014

Available online xxx


Keywords: Mucin Mucus CF

Goblet cells CFTR

22Q2 Mucociliary clearance 23 Pathogenesis

Our current understanding of cystic fibrosis (CF) has revealed that the biophysical properties of mucus play a considerable role in the pathogenesis of the disease in view of the fact that most mucus-producing organs are affected in CF patients. In this review, we discuss the potential causal relationship between altered cystic fibrosis transmembrane conductance regulator (CFTR) function and the production of mucus with abnormal biophysical properties in the intestine and lungs, highlighting what has been learned from cell cultures and animal models that mimic CF pathogenesis. A similar cascade of events, including mucus obstruction, infection and inflammation, is common to all epithelia affected by impaired surface hydration. Hence, the main structural components of mucus, namely the polymeric, gel-forming mucins, are critical to the onset of the disease. Defective CFTR leads to epithelial surface dehydration, altered pH/electrolyte composition and mucin concentration. Further, it can influence mucin transition from the intracellular to extracellular environment, potentially resulting in aberrant mucus gel formation. While defective HCO3 - production has long been identified as a feature of CF, it has only recently been considered as a key player in the transition phase of mucins. We conclude by examining the influence of mucins on the biophysical properties of CF sputum and discuss existing and novel therapies aimed at removing mucus from the lungs.

This article is part of a Directed Issue entitled: Cystic Fibrosis: From o-mics to cell biology, physiology, and therapeutic advances.

© 2014 Published by Elsevier Ltd.

25 Contents

26 1. Introduction....................................................................................................................................................................................................................................................................................00

27 2. Consequences of CFTR mutations for mucus..................................................................................................................................................................................................................00

28 2.1. Changes in mucus properties in the intestine................................................................................................................................................................................................00

29 2.2. Impact on mucociliary clearance in the lungs................................................................................................................................................................................................00

30 3. Polymeric, gel-forming mucins..............................................................................................................................................................................................................................................00

31 3.1. Intracellular mucin polymer formation and post-secretion expansion............................................................................................................................................00

32 3.2. Mucins in CF sputum....................................................................................................................................................................................................................................................00

33 4. Therapies aimed at removing mucus from the lungs ................................................................................................................................................................................................00

34 5. Conclusions......................................................................................................................................................................................................................................................................................00

35 Conflict of interest............................................................................................................................................................................................................................................................................00

36 Acknowledgements....................................................................................................................................................................................................................................................................00

37 References ........................................................................................................................................................................................................................................................................................00

* This article is part of a Directed Issue entitled: Cystic Fibrosis: From o-mics to cell biology, physiology, and therapeutic advances.

* Corresponding author at: CF/Pulmonary Research & Treatment Centre, 5101 Thurston-Bowles Bldg., The University of North Carolina at Chapel Hill, Campus Box #7248, USA. Tel.: +1 919 962 4718; fax: +1 919 966 5178.

E-mail addresses:, (C. Ehre). 1357-2725/© 2014 Published by Elsevier Ltd.


C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

1. Introduction

CF is the most common genetic disease, occurring prevalently in the Caucasian population at a rate of 1 in 2500 newborns of Northern European descent. The most common symptoms of CF include progressive lung disease and chronic digestive conditions, which are the result of mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) (Riordan et al., 1989). Depending on genetic and environmental factors, symptom severity varies among individuals carrying CFTR mutations. More specifically, CF pathogenesis is characterised by the build-up of thick, sticky mucus in multiple mucin-producing organs, such as the lungs, sinuses, intestine, pancreas and reproductive organs. For this reason, CF is also known as mucoviscidosis, suggesting that polymeric, gel-forming mucins, the large O-linked glycoproteins responsible for the vis-coelastic properties of mucus, play a critical role in the disease (Kreda et al., 2012).

Since the discovery of the defective CF gene in 1989, almost 2000 mutations have been reported and are available in the Cystic Fibrosis Mutation Database.1 The CFTR gene encodes for a cyclic adenosine monophosphate (cAMP) regulated chloride channel expressed in apical membranes of various epithelia (Gregory et al., 1990). In addition to controlling chloride secretion, this channel regulates the function of other membrane proteins, including the epithelial sodium channel (ENaC) (Briel et al., 1998). Both CFTR and ENaC play an important role in maintaining homeosta-sis by controlling the movement of water through the epithelium, which is particularly important for mucous membranes. Hence, CFTR malfunction leads to fluid hyperabsorption and subsequent dehydration of the epithelial surface, which, in turn, results in abnormal mucus gel with an increased polymeric mucin concentration and altered biophysical properties (Boucher, 2007; Button et al., 2012).

Among other tissues, CFTR is expressed in the pancreas, intestine, lungs, and reproductive tract, and each organ-specific phenotype can be related to the production of aberrant mucus with altered biophysical properties (Burgel et al., 2007; Malmberg et al., 2006; Reid et al., 1997). Common symptoms exhibited in mucin-producing organs are blocked ducts and impaired mucosal defence. In this review, we focus on the role of CFTR in the intestine and lungs since these organs have been the subjects of most studies involving the biophysical properties of mucins. By controlling fluid secretion and regulating ion composition in these organs, CFTR plays a critical role in mucosal defence by modulating the biophysical properties of mucus and assisting in bacterial killing (Norkina et al., 2004a; Pezzulo et al., 2012; Puchelle et al., 2002). Abnormal modulation of epithelial inflammation related to CFTR malfunction may further contribute to CF pathophysiology, but the link has yet to be established. CFTR also plays an important role in the transcellular secretion of bicarbonate (HCO3-), an alkalizing agent that plays a crucial physiological role in pH buffering. Although impaired bicarbonate secretion was reported early in the discovery of the disease (Hadorn et al., 1968), the role of this anion in CF has only recently been a major focus of interest within the mucus/mucin community. As highlighted by Quinton (2008), CF individuals suffer from complications in all mucin-secreting organs, which may be a consequence of defective HCO3- transport. Consistent with this idea, reduced HCO3- secretion in CF may be responsible for lowered epithelial surface pH, which has been shown to impede bacterial killing (Pezzulo et al., 2012) and increase mucus/mucin viscoelas-ticity (Celli et al., 2005; Georgiades et al., 2013). More specifically, there is emerging evidence that HCO3- plays a key role in the

expansion of polymeric mucins after their secretion into the extracellular milieu that is essential for normal mucus gel formation and transport (Chen et al., 2010; Cooper et al., 2013).

Before the use of physiotherapy (to remove mucus from the lungs) and enzyme therapy (e.g., pancreatic enzymes to correct digestive enzyme insufficiency and inhaled DNase treatment to alter mucus properties), CF was considered to be a fatal childhood disease. However, with improved therapies and strategies for managing the disease, the average life expectancy for CF patients is now 37 years.2 In recent years, small molecule therapies directed at restoring CFTR functionality have yielded success with a small number of mutations and are being pursued for other, more common mutations. Indeed, the goal of developing CFTR-specific therapies for all patients is currently a key objective of the Cystic Fibrosis Foundation. In the meantime, alternative approaches are being investigated (e.g., the use of mucolytics, inhibitors of mucin secretion and osmotic agents) to address the problem of mucus accumulation/obstruction in CF patients. In this article, we will review the current understanding of mucus and mucins in CF, describe how inefficient post-secretory mucin expansion may result in mucus with aberrant physical properties, and conclude by discussing therapies aimed at removing mucus from the lungs.

2. Consequences of CFTR mutations for mucus

The molecular mechanisms by which CFTR mutations can disrupt CFTR function include defects in protein synthesis (class I), maturation/trafficking (class II, e.g., AF508, the most common mutation with nearly 90% of patients carrying at least one allele), channel gating (class III, e.g. G551D, the target of Kalydeco; see Section 4), altered conductance (class IV) and decreased CFTR abundance (class V) (Ferec and Cutting, 2012). As mentioned above, these defects lead to deficient cAMP-dependent Cl- and HCO3-secretion and enhanced ENaC-mediated Na+ absorption in affected epithelia, resulting in dehydration of the mucus and concentration of its components (e.g., mucins) (Boucher, 2007). As a result, the majority of CF patients require a daily routine of inhaled therapies and exercise to prevent the progression of lung disease or a decrease in lung function. Additionally, most CF patients suffer from gastrointestinal (GI) manifestations regardless of their genotype. A similar pathogenesis cascade of obstruction, infection and inflammation is observed in the airways and intestines and is thought to be the direct result of epithelial surface dehydration and abnormal electrolyte composition.

2.1. Changes in mucus properties in the intestine

Expression of the CFTR gene in the GI tract is low in the stomach and rises in the intestine, displaying a gradient with the highest mRNA levels in the duodenum and lowest levels in the large intestine (Strong et al., 1994). This pattern of expression may reflect the need for acid neutralisation via HCO3- secretion as the proximal intestine receives a highly acidic bolus from the stomach. In addition to exhibiting high levels of CFTR expression, the normal intestine receives large volumes of HCO3--rich material from the pancreas. Proper pH buffering and fluid secretion in the intestine is essential for the optimal functioning of digestive enzymes and the maintenance of normal bacterial flora. In the case of CF, the combination of prolonged acidity following food uptake and dehydrated intestinal mucus facilitates bacterial growth in the GI tract (De Lisle and Borowitz, 2013; Fridge et al., 2007; Lisowska et al., 2009). Mucus adhesion to the intestinal wall may be related to mucin

100 101 102

110 111 112



C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

hyperconcentration and/or abnormal mucin expansion upon granule exocytosis (Garcia et al., 2009; Kesimer et al., 2010; Verdugo, 2012b); this latter process will be discussed in more depth, below (see Section 3.1). The most serious acute complication of the CF intestinal phenotype is the obstruction of the terminal ileum or proximal large intestine, referred to as meconium ileus, which occurs frequently in CF neonates with severe genotypes (Feingold and Guilloud-Bataille, 1999). Meconium ileus, which is a complex, mucin-rich substance (Schachter and Dixon, 1965), can be surgically removed or washed out with osmotic agents but if untreated can result in the rupture of the intestinal wall and sepsis (De Lisle and Borowitz, 2013). Other consequences of CFTR mutations in the intestine include an abnormal GI microbiota with altered diversity, location and density, and increased inflammation, which leads to ulcerations in 60% of CF patients as revealed by a new endoscopy technique relying on swallowed capsules (PillCam) (Werlin et al., 2010).

Gene-targeted animal models (e.g., mice, pigs and ferrets) lacking CFTR or Cftr expression develop meconium ileus at birth, confirming the importance of CFTR in the GI tract (Rogers et al., 2008; Snouwaert et al., 1992; Sun et al., 2010). Cftr mutant mouse models, which include both Cftr point mutations (e.g., CftrAF508/AF508) and complete Cftr knockouts (e.g., Cftr-/-), have greatly contributed to our understanding of the GI manifestations of CF. However, Cftr mutant mice develop only mild lung pheno-types, likely due to compensation mechanisms that stimulate other Cl- channels, such that these mice are not as effective for studying CF lung pathogenesis. The major intestinal phenotypes in CF mouse models are obstruction, bacterial colonisation and inflammation (Guilbault et al., 2007; Lynch et al., 2013). Mucus adhesion contributes to bacterial colonisation in CF mice, which can be alleviated by laxative treatment (De Lisle et al., 2007). Although a direct causal relationship between bacterial colonisation and inflammation has not yet been established, CF mice exhibit increased levels of neutrophils, mast-cells and inflammatory markers (Norkina et al., 2004b).The slow intestinal transit due to abnormal mucus biophysical properties appears to initiate a cascade of events that promote chronic bacterial infection and inflammation.

2.2. Impact on mucociliary clearance in the lungs

Although CFTR mutations affect several organs, the progression of lung disease can be particularly life-threatening. Despite much improvement in therapies, pulmonary complications are still the major cause of morbidity and mortality in CF patients. CF patients experiencing a rapid decline in lung function typically display poor survival rate unless they undergo lung transplantation (Rosenbluth et al., 2004). The production of "abnormal" mucus with aberrant rheological properties in the lungs leads to a cascade of events that involve mucus adhesion to epithelial surfaces, airway plugging, chronic bacterial infection and inflammation (Button et al., 2012; Mall et al., 2004; Stoltz et al., 2010). Once these early events (i.e., mucus stasis and/or bacterial infection) take place in the lungs, complex feedback mechanisms ensue. For instance, bacterial infection stimulates goblet cell hyperplasia and the recruitment of neutrophils (Cash et al., 1979), which worsen mucus viscosity and reduce clearance via the release of extracellular DNA (Lethem et al., 1990; Shak et al., 1990). Impaired clearance facilitates bacterial growth and biofilm formation, triggering more inflammation (Davies, 2002; Stoltz et al., 2010). Recently, much effort from the scientific community has focused on the specific mechanisms underlying the onset of lung disease in CF patients; i.e., whether mucin concentration or impaired bacterial killing alone can prompt CF lung pathogenesis.

In CF, airway dehydration leads to airway surface liquid (ASL) volume depletion, increased mucus concentration and reduced

mucociliary clearance (MCC) (Boucher, 2007; Matsui et al., 1998). 221

Specifically, increased mucin concentration causes the osmotic 222

pressure of the mucus layer to increase, which draws water osmot- 223

ically from the periciliary layer (PCL) that is occupied, in part, by 224

cell-surface tethered mucins (Button et al., 2012; Kesimer et al., 225

2013). Beyond a critical concentration of 5% solids, the osmotic 226

pressure of the mucus layer exceeds the osmotic pressure of the 227

PCL, initiating the collapse of the PCL. As a result of this collapse, 228

cilia are compressed and unable to beat. The mucus layer adheres to 229

the cell surfaces of the epithelium, causing MCC to cease. Mucus sta- 230

sis eventually leads to airway plugging, chronic bacterial infection, 231

inflammation and airway tissue damage (bronchiectasis). 232

As mentioned earlier, Cftr mutant mice develop only mild lung 233

phenotypes. However, it was still possible to validate the hypothe- 234

sis that airway dehydration promotes mucus plugging and triggers 235

inflammation using a mouse model that overexpresses the P sub- 236

unit of the Na+ channel in the lungs, also called the PENaC mouse 237

(Mall et al., 2004). This model has demonstrated that acceler- 238

ated Na+ transport alone produces a CF-like lung phenotype that 239

exhibits PCL collapse, slowed MCC rate, mucus obstruction and neu- 240

trophilic inflammation (Fig. 1). PENaC-overexpressing neonates 241

show a temporary increase in bacterial burden that appears to 242

resolve by adulthood (Livraghi-Butrico et al., 2012). Interestingly, 243

PENaC-overexpressing animals born and housed in germ-free 244

(gnotobiotic) and LPS-free conditions developed and maintained 245

an inflammatory phenotype, suggesting that mucus dehydration 246

alone is sufficient to trigger airway inflammation (Livraghi-Butrico 247

et al., 2012). These results imply that the epithelium responds to 248

an abnormal mucus layer by initiating the recruitment of neu- 249

trophils. These early events instigate a vicious cycle in the lungs 250

as dying neutrophils entrapped in thick mucus release their DNA 251

and worsen the rheological properties of mucus (Lethem et al., 252

1990; Shak et al., 1990). This thick, immobile mucus provides an 253

optimal environment for bacterial growth and, consequently, stim- 254

ulates further mucin release and neutrophil infiltration (Knowles 255

and Boucher, 2002; Smith, 1997; Wanner et al., 1996). 256

In contrast with the mouse, the CF pig model that expresses 257

a mutant form (-/A508) spontaneously develops the features 258

of CF lung disease, including infection (Stoltz et al., 2010). In 259

this model, airways can be completely occluded with tenacious, 260

adherent mucus, resembling mucus observed in human CF lungs. 261

Histopathology has revealed that these mucus plaques exhibit a 262

lamellar appearance, suggesting that the progressive deposition of 263

mucus is the result of slowed MCC. Within hours of birth (6-12 h), 264

CF pigs show no inflammation but increased bacterial burden. The 265

impaired ability to eradicate bacteria is related to lowered ASL pH, 266

which can be directly linked to the inability of CF airways to secrete 267

HCO3- (Pezzulo et al., 2012; Stoltz et al., 2010). Although HCO3- 268

plays a critical role in bacterial killing, the mucus obstructive phe- 269

notype is not exclusively related to defective HCO3- secretion since 270

the PENaC mouse model develops mucus plugging subsequent to 271

airway dehydration. 272

3. Polymeric, gel-forming mucins

The molecular framework and biophysical properties of mucus are provided in large part by the high-molecular-weight (Mr 2100 MDa) polymeric gel-forming mucins (Sheehan et al., 1986). Q3 The products of 5 genes (MUC genes), MUC2, MUC5AC, MUC5B, MUC6 and MUC19 in the human and Muc2, Muc5ac, Muc5b, Muc6 and Muc19 in the mouse (Chen et al., 2004; Escande et al., 2004; Thornton et al., 2008), make up this family of closely related O-linked glycoproteins (Fig. 2). Of particular relevance to this review are MUC2/Muc2 (Gum et al., 1994), the major intestinal mucin, and MUC5AC/Muc5ac and MUC5B/Muc5b, the major


C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

, 20 мт

Fig. 1. Formation of mucus plaques and neutrophilic inflammation in the pENaC mouse model. (A) AB-PAS stain of pENaC lungs revealing mucus plugs at airway branching. (B) Immunohistochemistry (IHC) displaying PCL collapse and mucin accumulation on airway surfaces (green = Muc5b, blue = DAPI). (C) Inflammatory cells from a pENaC mouse Q7 bronchoalveolar lavage showing a mixture of macrophages and neutrophils. (D) IHC exhibiting inflammatory cells trapped in mucus. (For interpretation of the references to color in this legend, the reader is referred to the web version of the article.)

respiratory mucins (Thornton et al., 2008). The physicochemical and biological properties of these mucins are dictated by their heavily glycosylated mucin domains. The dense glycosylation of these molecules (up to 80% in mass) with neutral and negatively charged O-glycans stiffens the mucin polypeptide, resulting in a high volume occupancy in solution which is important for gel-formation (Gerken, 1993). Furthermore, the extensive glycosylation protects the underlying mucin polypeptide from degradation by host and pathogen-proteases produced during inflammation and infection (Hasnain et al., 2012; Henke et al., 2011; Innes et al., 2009) and provides specific ligands for bacterial adhesins that influence the interaction of the host with commensal and pathogenic organisms (McGuckin et al., 2011).

Flanking the central glycosylated region are the N- and C-terminal cysteine-rich domains of the mucin monomers, which are important for intracellular disulphide-linked polymerisation (Asker et al., 1995, 1998a,b; Axelsson et al., 1998; Perez-Vilar and Hill, 1999); their role in this process will be discussed in more detail below. Other cysteine-rich domains (cys-domains) interrupt the central glycosylated regions of the mucin monomers and their number is different between mucins; MUC2, MUC5B and MUC5AC contain 2, 7 and 9 respectively (Rose and Voynow, 2006). The different patterns of interruption of the glycosylated domains coupled with the tissue-specific expression of the mucins (intestinal tract for MUC2 and respiratory tract for MUC5AC and MUC5B) implies different functions for MUC2 compared with MUC5AC and MUC5B. It has been suggested that cys-domains have a role in non-covalent, dynamic cross-linking of mucin polymers within mucus (Ambort

et al., 2011). One could hypothesise that their location between the stiffened, glycosylated regions of the mucin polypeptide would provide points of flexibility within the mucin polymers that might be important for the dynamic behaviour of the mucin polymers in mucus, and/or during their intracellular assembly. Moreover, cys-domains may provide sites for proteolytic cleavage for normal mucin turnover or degradation during infection/inflammation. Further research is needed to fully elucidate the function of these domains.

At the mucosal surfaces, mucins are produced mainly from specialised secretory cells: surface epithelial goblet cells (in the intestine and lungs) and glandular mucous cells (in the lungs). In these cells, the pre-assembled mucin polymers are stored, condensed and dehydrated within secretory granules (Verdugo, 1991). The release of mucin granules is regulated either by a baseline mechanism or a purinergic-induced secretory pathway (Davis and Dickey, 2008). Once secreted into the extracellular environment, mucins hydrate and expand to form a mucus gel with viscoelas-tic properties that depend on the entanglement of large mucin polymer chains (Georgiades et al., 2013; Raynal et al., 2002; Verdugo, 1987, 2012b). Other factors will influence the viscoelastic properties of mucus, including hydration status (i.e., mucin concentration), ionic environment, pH, and the degree of cross-linking (covalent and non-covalent bonds) between mucin polymeric chains and between mucins and other components of mucus (i.e., globular proteins) (Ambort et al., 2011, 2012; Georgiades et al., 2013; Raynal et al., 2003). Thus, CFTR malfunction and the resultant consequences for the epithelial surface (e.g., altered mucin


C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

Fig. 2. Cartoon of mucin structure and assembly. (A) Polymeric, gel-forming mucins all share a common structural architecture. The N- and C-terminal domains have a high cysteine content and these form intra- and intermolecular disulphide bonds. The central highly-glycosylated domains (mucin domains) are enriched in serine, threonine and proline residues and the O-glycans are covalently attached, via the linkage sugar N-acetylgalactosamine, to serine and threonine residues. The O-glycan chains are comprised of N-acetylglucosamine, galactose, N-acetylgalactosamine, fucose and sialic acid; galactose can be modified by sulphation. The number, length and amino acid sequence of these glycosylated domains differ between mucins. The glycosylated domains are interrupted with cys-domains, and the number of these cysteine-rich regions differs Q8 between mucins. For more detailed reviews on the primary structure of MUC2, MUC5AC and MUC5B the reader is referred to the following articles - Dekker et al. (2002) and Rose and Voynow (2006). (B) The early steps in polymeric mucin assembly are well accepted. In the endoplasmic reticulum (ER), the non-O-glycosylated polypeptide forms dimers via disulphide bonds formed between the CK-domains. In the Golgi/trans-Golgi network (TGN), mucin dimers are O-glycosylated and then multimerise by disulphide bonds formed between N-terminal D3 domains. There are two mechanisms proposed for this step, multimers form from dimers of dimers (MUC5B, Ridley et al., 2011; Round et al., 2004; Sheehan et al., 2004; Thornton et al., 1990) ortrimers of dimers (MUC2, Ambort et al., 2012). The mucin multimers are then packaged in an ordered state within secretory granules. The acidic pH inside the granules and their high Ca2+ content facilitates mucin organisation via non-covalent interactions between mucin N-termini (Ambort et al., 2012). After secretion mucins hydrate and expand to form mucus.

340 and electrolyte concentrations and abnormal pH) will have major

341 effects on the propensity of mucus gel-formation. In particular, a

342 current focus of mucin-related research in CF is the mechanism of

343 intracellular mucin polymer formation and the role of HCO3- in

344 their transition from an intracellular to extracellular form.

345 3.1. Intracellular mucin polymer formation and post-secretion

346 expansion

347 The intracellular assembly of polymeric mucins, as detailed in

348 Fig. 2, is a complex process. Disulphide-linkage between C-terminal

domains yields dimers, which are subsequently polymerised via N- 349

terminal disulphide bonding (Asker et al., 1995,1998a,b; Axelsson 350

et al., 1998; Perez-Vilar and Hill, 1999). The molecular details of 351

intracellular mucin polymer formation have best been described 352

for the intestinal mucin, MUC2, and have yet to be fully elucidated 353

for the respiratory mucins, MUC5AC and MUC5B. In brief, MUC2 354

dimers are reported to polymerise via N-terminal trimerisation to 355

yield branched polymers (Ambort et al., 2012; Godl et al., 2002), 356

whereas MUC5B and MUC5AC dimers polymerise via N-terminal 357

dimerisation to form linear polymers (Ridley et al., 2011; Round 358

et al., 2004; Sheehan et al., 2004; Thornton et al., 1990). Whatever 359


C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

360 the mechanism of polymer assembly, it has become increasingly

361 clear that mucin polymers are highly organised within the secretory

362 granules (Ambort et al., 2012; Kesimer et al., 2010), and that this is

363 necessary in order to control their rapid expansion after secretion

364 into the extracellular environment to form mucus (see Verdugo,

365 2012a for an in-depth discussion of the biophysics and dynamics

366 of post-secretory mucin expansion).

367 It has been proposed that Ca2+ ions have critical roles in the

368 intragranular organisation of mucins. It has long been accepted

369 that shielding the negative charge associated with the O-glycans

370 (sialic acid and sulphate groups) by Ca2+ ions facilitates mucin

371 compaction (Kuver and Lee, 2004; Verdugo et al., 1987). More

372 recently, it has been suggested that Ca2+ ions, in the acidic pH

373 environment of the granule, organise the N-termini of MUC2 into

374 6-membered ring-like structures that facilitate efficient packing

375 (Ambort et al., 2012). These authors proposed a novel model for the

376 highly organised packing of MUC2 within the granule, and how this

377 facilitates the unpacking necessary to form the lamellar structure

378 reported for MUC2-rich mucin gels (Round et al., 2012). How-

379 ever, this model remains controversial and is incompatible with

380 the swelling kinetics and behaviour of mucins as they expand after

381 secretion (Verdugo, 2012a,b). Moreover, whether this model can be

382 generalised to MUC5AC and MUC5B, which form linear rather than

383 branched polymers, has yet to be determined. Electron microscopy

384 images of salivary mucins suggest that intragranular MUC5B is not

385 packaged as a random coil but exists as a cross-linked structure

386 that is organised around 'nodes' containing the terminal protein

387 domains of the mucin polypeptide (Kesimer et al., 2010). How-

388 ever, the involvement of Ca2+ ions in these 'nodes' has not been

389 determined.

390 Upon mucin exocytosis onto the hydrated epithelial surface,

391 Ca2+ ions are exchanged for Na+ ions and pH is increased, leading to

392 a rapid expansion of the mucin polymers (Verdugo, 1991, 2012b).

393 Although we currently have an incomplete understanding of the

394 mechanism controlling this critical transition, it has been shown

395 that HCO3 - ions in the luminal milieu play an important role in

396 mucin expansion by sequestering Ca2+ ions and promoting alka-

397 linisation, thereby facilitating efficient expansion and hydration of

398 the glycosylated mucin domains (Chen et al., 2010; Gustafsson et al.,

399 2012; Quinton, 2010). This suggests that a critical function of CFTR

400 is regulating of the viscoelastic properties of mucus, and that HCO3 -

401 is in short supply during the course of mucin granule exocytosis in

402 patients with CF. Defective HCO3 - -mediated post-secretory mucin

403 expansion coupled with defective hydration likely causes intestinal

404 blockage (Garcia et al., 2009) and airway obstruction (Cooper et al.,

405 2013). One of the striking phenotypes exhibited by CF mice, besides

406 mecomium ileus, is the production of abnormal ileal mucus that is

407 adherent to the epithelium. This mucus is two or three times denser

408 than mucus of wild-type (WT) mice and less penetrable to beads the

409 size of bacteria (Gustafsson et al., 2012). Remarkably, in this mouse

410 model, CF mucus properties appear to be normalised when mucins

411 are secreted into buffers containing 115 mM HCO3- or20mM EDTA

412 (Gustafsson et al., 2012), likely due to sequestration of Ca2+ ions that

413 allow mucins to expand. In addition, the volume of CF mucus (but

414 not WT mucus) increases in a HCO3--enriched milieu, suggesting

415 that CF mucus is incompletely expanded (Ambort et al., 2012).

416 The use of CF mice has provided a better understanding of, and

417 new insights into the importance of HCO3- in the expansion of

418 mucins, particularly MUC2/Muc2. Whether this new knowledge

419 can be generalised to respiratory mucins is not yet clear because the

420 mechanisms of polymerisation for MUC5AC and MUC5B have yet to

421 be determined. Intestinal mucus has been described as a chemical

422 gel where the mucin matrix is formed from branched polymers (as

423 a result of N-terminal trimerisation; Fig. 2), resulting in a covalently

424 cross-linked gel network (Ambort et al., 2011; Hong et al., 2005).

425 In contrast, respiratory mucus is a physical gel in which linear

polymers (as a result of N-terminal dimerization; Fig. 2) are 426

entangled and maintained in close proximity by electrostatic and 427

hydrophobic bonds (Sheehan et al., 2004; Thornton et al., 2008). 428

These different mucin network organisations may be related to 429

the different functional requirements of their respective organs. In 430

the intestine, a tight mucin network with limited swelling capacity 431

might provide the best protection against the passage of large vol- 432

umes of gastric juice and partially digested food. On the other hand, 433

the respiratory tract might benefit from airway mucus that is more 434

dynamic, allowing for the precise tuning of its rheological prop- 435

erties for optimal MCC and, at the same time, ensuring bacterial 436

trapping. 437

3.2. Mucins in CF sputum 438

MUC5AC and MUC5B are the major gel-forming mucins pro- 439

duced in the lungs. Traditionally, their function has been viewed as 440

a 'catch-all' barrier to trap inhaled pathogens, particulates that are 441

continuously removed from the lungs by the coordinated beating 442

of cilia. The specific roles of MUC5AC and MUC5B have been largely 443

undetermined until recently. Further, the O-glycans coating these 444

mucins may have diverged, evolutionary, to suit the needs of dif- 445

ferent species. Nonetheless, mouse models generated to examine 446

the role of mucins have revealed that Muc5ac provides protec- 447

tion against viral infection by acting as a decoy for viral receptors 448

(Ehre et al., 2012), while Muc5b is essential for MCC and control- 449

ling bacterial infection (Muc5ac appears dispensable for these latter 450

functions) (Roy et al., 2013). 451

Analysis of CF sputum mucin content has revealed increased 452

MUC5AC and MUC5B concentrations (especially following exacer- 453

bations) with MUC5B being the predominant mucin (Henke et al., 454

2007; Horsley etal.,2013; Kirkhametal.,2002).Likewise, immuno- 455

histochemical analysis has demonstrated increased concentrations 456

MUC5AC and MUC5B in the mucus plugs of CF airways when com- 457

pared to normal controls, again, with a higher relative abundance 458

of MUC5B (Burgel et al., 2007). Analysis of the macromolecular 459

properties of polymeric mucins in CF sputum has shown that they 460

are, on average, smaller compared to normal mucins, likely due 461

to the increased proteolytic activity of CF sputum (Davies et al., 462

2002; Gupta and Jentoft, 1992; Rose et al., 1987; Thornton et al., 463

1991). Intriguingly, a significant genetic association was found 464

between the length of the gene region encoding the MUC5AC 465

variable number of tandem repeats (VNTR) and CF lung disease 466

severity. However, the mechanisms underlying this association 467

remain obscure (Guo et al., 2011). 468

While CF mucus exhibits an altered composition of mucins, 469

there are no major changes in the macromolecular properties of 470

the mucins that might explain the sub-optimal mucus transport 471

properties. Mucins isolated from expectorated sputum have not 472

been reported to contain cross-linked species that could represent 473

the unexpanded, intragranular form. However, this molecular form 474

may be more highly represented in adherent mucus plaques that 475

are not expectorated. Detailed molecular analysis of the lamellar- 476

structured plaques found in the CF pig airways might shed light on 477

this issue. 478

In contrast to normal respiratory mucus, the physical properties 479

of CF sputum are not wholly due to polymeric mucins but arise from 480

a complex interaction between the mucins and other sputum com- 481

ponents, including cell surface mucins, DNA and actin, as well as 482

inflammatory cells, bacteria, viruses and exoproducts (Matthews 483

et al., 1963; Voynow and Rubin, 2009). As a result, the airways 484

clearance of mucus that occurs through the coordinated beating 485

of cilia is compromised; however, the influence of these different 486

components on the aberrant rheological properties of sputum is 487

incompletely understood. The importance of mucins as opposed 488

to other macromolecules, particularly DNA, in determining the 489


C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

viscoelastic properties of CF sputum has been questioned (Henke et al., 2004). However, the biophysical properties of mucins in CF secretions may have been underestimated as a result of proteolytic degradation, rendering rheological assays inaccurate and difficult to perform (Horsley et al., 2013). Moreover, proteolysis would explain observations suggesting mucin levels were lower in CF sputum than in healthy controls (Henke et al., 2004). Nonetheless, the clinical benefits associated with treatments aimed at improving mucus clearance have been clearly demonstrated in CF patients. Typically, removal of thickened, adhered, mucus relies on physical (i.e., physiotherapy) and/or chemical (i.e., orally administered or inhaled medications) therapies. Indeed, agents aimed at improving mucin solubilisation will have an important role in the treatment of CF lung disease.

4. Therapies aimed at removing mucus from the lungs

Therapeutic strategies targeting the underlying cause of CF (i.e., CFTR malfunction) offer important benefits for CF patients as compared to treating a wide range of symptoms. Thus, for the first 10-15 years following the discovery of the gene defect in CF, research towards correcting the defect by gene therapy was a major focus of the CF community. However, it was eventually realised that gene transfer into diseased lungs was going to be more difficult than originally anticipated, likely due to a physical barrier produced by persistent mucus production and the short-lived expression of the delivered therapeutic gene (Griesenbach et al., 2003). This led to greater exploration of alternative approaches for correcting CFTR malfunction. More recently, high-throughput screening programmes for the identification of compounds capable of restoring CFTR function (see Section 2) were initiated by the Cystic Fibro-sis Foundation and lead to the discovery of Ivacaftor (Kalydeco or VX-770) by Vertex Pharmaceuticals Inc. In vitro, Ivacaftor was shown to increase Cl- -transport activity of cell lines expressing the G551D-CFTR mutation by increasing the time the channel remained open at the cell surface (i.e., it is a CFTR potentiator) (Van Goor et al., 2009). Approximately 4-5% of CF patients carry the G551D mutation, limiting the impact of this oral drug on the global CF population (McKone et al., 2003). Nevertheless, the treatment of G551D patients was associated with rapid and sustained improvement in lung function (FEV1), reduced pulmonary exacerbations and respiratory symptoms, weight gain and increased sweat chloride concentration (Accurso et al., 2010; Ramsey et al., 2011). In addition, remarkable improvements in mucociliary clearance and ventilation defects have been shown during treatment with Iva-caftor, suggesting that restitution of CFTR function is sufficient to normalise the aberrant properties of mucus (Altes et al., 2012; Donaldson et al., 2013). Currently, two large clinical trials testing the effects of Ivacaftor in combination with a CFTR corrector (VX-809) in patients carrying the most common mutation (AF508) are being conducted, based upon promising results in earlier studies, including a significant improvement in lung function (Boyle et al., 2012).

Although correcting the underlying cause of CF is an overarching goal and appears to restore mucociliary clearance (Altes et al., 2012; Donaldson et al., 2013), alternative therapies that reduce airway mucus obstruction (mucolytics) have been used for decades and novel therapies with this particular aim are currently being investigated. The discovery that CF secretions contain substantial amounts of extracellular DNA led to the development of a recombinant human DNase I (rhDNase or Dornase a or Pulmozyme®) by Genentech Inc. in the 1990s. Initially, in vitro experiments confirmed that rhDNase decreased the viscosity of CF sputum (Shak et al., 1990). Hence, rhDNase was tested in patients via inhalation and resulted in reduced exacerbations and respiratory symptoms,

as well as improved FEV1 (Fuchs et al., 1994; Ramsey et al., 1993). Over the past two decades, rhDNase has been routinely used for CF patient care as a means of clearing mucopurulent mucus, but alone is not completely effective at alleviating the problems associated with mucus overproduction and airway obstruction.

Since breaking down large DNA molecules improves respiratory symptoms, it is reasonable to postulate that reducing the size of mucin polymers may also benefit airway clearance. The use of N-acetylcysteine (NAC), a reducing agent that targets disulphide bonds between mucin monomers and results in depolymerisation, was approved in the 1960s and has been used as both an oral and inhaled therapy. Surprisingly, inhalation of 20% NAC (1.2 M) has not yielded clinical benefits, as reviewed by two independent Cochrane studies (Nash et al., 2009; Tam et al., 2013). It could be argued that the lack of clinical benefits with NAC is related to decreased mucin concentration and that DNA is the major contributor to the properties of mucus in CF (Henke and Ratjen, 2007). Alternatively, NAC might simply be a weak reducing agent that is ineffective at the concentrations deposited in the lower airways. Although this notion needs to be further investigated, the development of more potent reducing agents with increased efficacy may present important clinical benefits for CF patients.

Controlling the rate of mucin secretion has also been considered as a way to alleviate airway obstruction in CF. Understanding the regulation of mucin granule exocytosis is essential for this approach, and studies have shown similarities between the exo-cytic mechanism in mucin-producing cells and other secretory cells, such as neurons (Burgoyne and Morgan, 2003; Davis and Dickey, 2008). Goblet cell secretagogues include P2Y2 receptor agonists (ATP and UTP) and other agents that cause intracellular Ca2+ mobilisation (Davis and Dickey, 2008; Kreda et al., 2007). The identification of downstream effectors of these secretagogues is essential to advancing a mucin regulatory approach. Inhibition of key components of the mucin exocytotic pathway, such as Munc13-2, VAMP8, ROCK, MARCKS, can inhibit the release of mucin granules and are currently being tested as potential drug targets (Jones et al., 2012; Kreda et al., 2010, 2012; Singer et al., 2004; Zhu et al., 2008).

Perhaps the simplest approach to removing mucus from the lungs is the use of osmotically active agents that rehydrate mucus. Inhalation of hypertonic saline has been shown to reduce pulmonary exacerbation, as well as improve FEV1 and MCC (Donaldson et al., 2006; Elkins et al., 2006). Another osmotically active agent, mannitol, has recently been shown to yield similar benefits (Bilton et al., 2013; Daviskas et al., 2010). Given the diversity of CFTR mutations, mucolytics, regulators of mucin secretion and osmotic agents may present several advantages over CFTR correctors/potentiators, such as being cheaper and generic for all CFTR mutations. Additional benefits related to the removal of mucus, besides improved airflow, might include reduced bacterial infection and inflammation.

5. Conclusions

Although much work is still needed to fully understand the causal relationship between defective CFTR function and the production of aberrant mucus, significant progress towards this goal has been made in recent years. Better insights of the CF pathogenesis cascade have arisen from a variety of sources, including primary cell culture, animal models, and also human patients, with studies performed on native tissues or intact organs. Hence, in some cases, translation of these findings to the general CF population may not be a straightforward process. In this review, we have tentatively summarised this progress, taking into account some inadvertent omissions and misconceptions. The relationship between impaired CFTR function and the production of sticky, viscous mucus in several organs is not always obvious but can be related to two


C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

physiological roles of the channel. By controlling water movement and HCO3- secretion, CFTR plays an essential role in the hydration and expansion of the mucins that are normally and continuously produced to protect mucosal surfaces. In CF, a water/electrolyte imbalance compromises the formation of the mucus gel that lines the mucosa and triggers a cascade of events with complex feedback mechanisms. In the lungs, the onset of mucus obstruction, infection and inflammation can be life-threatening. Hence, removal of mucus and mucopurulent material from the lungs is crucial for CF patients. Currently, translational research is being conducted to identify a number of compounds that offer promising pharmacotherapy for CF. More specifically, inhaled mucolytic agents have the potential to improve airflow, prevent bacterial growth and reduce inflammation and tissue damage. Targeting mucin intramolecular disulphide bonds using reducing agents is an interesting approach that could also benefit patients suffering from chronic obstructive pulmonary disease (COPD). Conceptually, this type of treatment would be used as an acute therapy (e.g., for exacerbation) rather than on a daily basis. Importantly, safety issues related to the reduction of other disulphide bonds would have to be considered. For example, the specificity of the target (i.e., mucins) over other luminal proteins will be difficult to achieve and necessitate monitoring. However, the side effects of such a treatment might be outweighed by its clinical benefits if it can effectively "clean" the lungs.

Conflict of interest

The authors declare no conflict of interest.


The authors wish to thank the NIH (NHLBI R01-HL116228) and the Cystic Fibrosis Foundation Therapeutics, Inc. (EHRE07XX0 and THORNTO7XX0).


Accurso FJ, Rowe SM, Clancy JP, Boyle MP, Dunitz JM, Durie PR, et al. Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation. N Engl J Med 2010;363:1991-2003.

Altes T, Johnson MA, Miller GW, MuglerJP, Flors L, Mata J, et al. Hyperpolarized gas MRI of Ivacaftor therapy in persons with cystic fibrosis and the G551D-CFTR mutation. Pediatr Pulmonol 2012;Suppl. 35:291.

Ambort D, Johansson ME, Gustafsson JK, Nilsson HE, Ermund A, Johansson BR, et al. Calcium and pH-dependent packing and release ofthe gel-forming MUC2 mucin. Proc Natl Acad Sci U S A 2012;109:5645-50.

Ambort D, van der Post S, Johansson ME, Mackenzie J, Thomsson E, Krengel U, et al. Function of the CysD domain of the gel-forming MUC2 mucin. Biochem J 2011;436:61-70.

Asker N, Axelsson MA, Olofsson SO, Hansson GC. Dimerization of the human MUC2 mucin in the endoplasmic reticulum is followed by a N-glycosylation-dependent transfer ofthe mono- and dimers to the Golgi apparatus. J Biol Chem 1998a;273:18857-63.

Asker N, Axelsson MA, Olofsson SO, Hansson GC. Human MUC5AC mucin dimerizes in the rough endoplasmic reticulum, similarly to the MUC2 mucin. Biochem J 1998b;335(Pt 2):381-7.

Asker N, Baeckstrom D, Axelsson MA, Carlstedt I, Hansson GC. The human MUC2 mucin apoprotein appears to dimerize before O-glycosylation and shares epi-topes with the 'insoluble' mucin of rat small intestine. Biochem J 1995;308(Pt 3):873-80.

Axelsson MA, Asker N, Hansson GC. O-glycosylated MUC2 monomer and dimer from LS 174T cells are water-soluble, whereas larger MUC2 species formed early during biosynthesis are insoluble and contain nonreducible intermolecular bonds. J Biol Chem 1998;273:18864-70.

Bilton D, Daviskas E, Anderson SD, Kolbe J, King G, Stirling RG, et al. Phase 3 randomized study of the efficacy and safety of inhaled dry powder manni-tol for the symptomatic treatment of non-cystic fibrosis bronchiectasis. Chest 2013;144:215-25.

Boucher RC. Cystic fibrosis: a disease ofvulnerability to airway surface dehydration. Trends Mol Med 2007;13:231-40.

Boyle MP, Bell SC, Konstan MW, McColley SA, Kang L, Patel N. The investigational CFTR corrector, VX-809 (Lumafactor) co-administered with the oral potentiator Ivacaftor improved CFTR and lung function in F508Del homozygous patients: phase II study resutls. Pediatr Pulmonol 2012 [Abstract #260].

Briel M, Greger R, Kunzelmann K. Cl-transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC. J Physiol 1998;508(Pt 3):825-36.

Burgel PR, Montani D, Danel C, Dusser DJ, Nadel JA. A morphometric study of mucins and small airway plugging in cystic fibrosis. Thorax 2007;62:153-61.

Burgoyne RD, Morgan A. Secretory granule exocytosis. Physiol Rev 2003;83:581-632.

Button B, Cai LH, Ehre C, Kesimer M, Hill DB, Sheehan JK, et al. A periciliary brush promotes the lung health by separating the mucus layer from airway epithelia. Science 2012;337:937-41.

Cash HA, Woods DE, McCullough B, Johanson WG Jr, Bass JA. A rat model of chronic respiratory infection with Pseudomonas aeruginosa. Am Rev Respir Dis 1979;119:453-9.

Celli J, Gregor B, Turner B, Afdhal NH, Bansil R, Erramilli S. Viscoelastic properties and dynamics of porcine gastric mucin. Biomacromolecules 2005;6:1329-33.

Chen EY, Yang N, Quinton PM, Chin WC. A new role for bicarbonate in mucus formation. Am J Physiol Lung Cell Mol Physiol 2010;299:L542-9.

Chen Y, Zhao YH, Kalaslavadi TB, Hamati E, Nehrke K, Le AD, et al. Genome-wide search and identification of a novel gel-forming mucin MUC19/Muc19 in glandular tissues. Am J Respir Cell Mol Biol 2004;30:155-65.

Cooper JL, Quinton PM, Ballard ST. Mucociliary transport in porcine trachea: differential effects of inhibiting chloride and bicarbonate secretion. Am J Physiol Lung Cell Mol Physiol 2013;304:L184-90.

Davies JC. Pseudomonas aeruginosa in cystic fibrosis: pathogenesis and persistence. Paediatr Respir Rev 2002;3:128-34.

Davies JR, Herrmann A, Russell W, Svitacheva N, Wickstrom C, Carlstedt I. Respiratory tract mucins: structure and expression patterns. Novartis Found Symp 2002;248:76-88 [discussion -93, 277-82].

Davis CW, Dickey BF. Regulated airway goblet cell mucin secretion. Annu Rev Physiol 2008;70:487-512.

Daviskas E, Anderson SD, Jaques A, Charlton B. Inhaled mannitol improves the hydration and surface properties of sputum in patients with cystic fibrosis. Chest 2010;137:861-8.

De Lisle RC, Borowitz D. The cystic fibrosis intestine. Cold Spring Harb Perspect Med 2013;3:a009753.

De Lisle RC, Roach E, Jansson K. Effects of laxative and N-acetylcysteine on mucus accumulation, bacterial load, transit, and inflammation in the cystic fibrosis mouse small intestine. Am J Physiol Gastrointest Liver Physiol 2007;293:G577-84.

Donaldson SH, Bennett WD, Zeman KL, Knowles MR, Tarran R, Boucher RC. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. N Engl J Med 2006;354:241-50.

Donaldson SH, Zeman K, Laube B, Corcoran T, Locke LW, Pilewski J, et al. Effect of Ivacaftor on mucociliary clearance and mucus rheology in patients with G551D-CFTR mutation. Pediatr Pulmonol 2013;Suppl. 36.

Ehre C, Worthington EN, Liesman RM, Grubb BR, Barbier D, O'Neal WK, et al. Overex-pressing mouse model demonstrates the protective role ofMuc5ac inthe lungs. Proc Natl Acad Sci U S A 2012;109:16528-33.

Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, Marks GB, et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006;354:229-40.

Escande F, Porchet N, Bernigaud A, Petitprez D, Aubert JP, Buisine MP. The mouse secreted gel-forming mucin gene cluster. Biomed Biochim Acta 2004;1676:240-50.

Feingold J, Guilloud-Bataille M. Genetic comparisons of patients with cystic fibrosis with or without meconium ileus. Clinical Centers ofthe French CF Registry. Adv Genet 1999;42:147-50.

Ferec C, Cutting GR. Assessing the disease-liability of mutations in CFTR. Cold Spring Harb Perspect Med 2012;2:a009480.

Fridge JL, Conrad C, Gerson L, Castillo RO, Cox K. Risk factors for small bowel bacterial overgrowth in cystic fibrosis. J Pediatr Gastroenterol Nutr 2007;44: 212-8.

Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, Ramsey BW, et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group. N Engl J Med 1994;331:637-42.

Garcia MA, Yang N, Quinton PM. Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion. J Clin Invest 2009;119:2613-22.

Georgiades P, Pudney PD, Thornton DJ, Waigh T. Particle tracking microrheology of purified gastrointestinal mucins. Biopolymers 2013.

Gerken TA. Biophysical approaches to salivary mucin structure, conformation and dynamics. Crit Rev Oral Biol Med 1993;4:261-70.

Godl K, Johansson ME, Lidell ME, Morgelin M, Karlsson H, Olson FJ, et al. The N terminus of the MUC2 mucin forms trimers that are held together within a trypsin-resistant core fragment. J Biol Chem 2002;277:47248-56.

Gregory RJ, Cheng SH, Rich DP, Marshall J, Paul S, Hehir K, et al. Expression and characterization of the cystic fibrosis transmembrane conductance regulator. Nature 1990;347:382-6.

Griesenbach U, Geddes DM, Alton EW. Update on gene therapy for cystic fibrosis. CurrOpin Mol Ther 2003;5:489-94.

Guilbault C, Saeed Z, Downey GP, Radzioch D. Cystic fibrosis mouse models. Am J Respir Cell Mol Biol 2007;36:1-7.

Gum JR Jr, Hicks JW, Toribara NW, Siddiki B, Kim YS. Molecular cloning of human intestinal mucin (MUC2) cDNA. Identification of the amino terminus

Q5 725

753 Q6 754


C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx 9

770 and overall sequence similarity to prepro-von Willebrand factor. J Biol Chem McGuckin MA, Linden SK, Sutton P, Florin TH. Mucin dynamics and enteric 856

771 1994;269:2440-6. pathogens. Nat Rev Microbiol 2011;9:265-78. 857

772 Guo X, Pace RG, Stonebraker JR, Commander CW, Dang AT, Drumm ML, et al. Mucin McKone EF, Emerson SS, Edwards KL, Aitken ML. Effect of genotype on phe- 858

773 variable number tandem repeat polymorphisms and severity of cystic fibrosis notype and mortality in cystic fibrosis: a retrospective cohort study. Lancet 859

774 lung disease: significant association with MUC5AC. PLoS ONE 2011;6:e25452. 2003;361:1671-6. 860

775 Gupta R, Jentoft N. The structure of tracheobronchial mucins from cystic fibrosis and NashEF, Stephenson A, Ratjen F, Tullis E. Nebulized and oral thiol derivatives for pul- 861

776 control patients. J Biol Chem 1992;267:3160-7. monary disease in cystic fibrosis. Cochrane Database Syst Rev 2009:CD007168. 862

777 Gustafsson JK, Ermund A, Ambort D, Johansson ME, Nilsson HE, Thorell K, et al. Norkina O, Burnett TG, De Lisle RC. Bacterial overgrowth in the cystic fibrosis trans- 863

778 Bicarbonate and functional CFTR channel are required for proper mucin secre- membrane conductance regulator null mouse small intestine. Infect Immun 864

779 tion and link cystic fibrosis with its mucus phenotype. J Emerg Med 2012;209: 2004a;72:6040-9. 865

780 1263-72. Norkina O, Kaur S, Ziemer D, De Lisle RC. Inflammation of the cystic fibrosis mouse 866

781 Hadorn B, Zoppi G, Shmerling DH, Prader A, McIntyre I, Anderson CM. Quantitative small intestine. Am J Physiol Gastrointest Liver Physiol 2004b;286:G1032-41. 867

782 assessment of exocrine pancreatic function in infants and children. J Pediatr Perez-Vilar J, Hill RL. The structure and assembly of secreted mucins. J Biol Chem 868

783 1968;73:39-50. 1999;274:31751-4. 869

784 Hasnain SZ, McGuckin MA, Grencis RK, Thornton DJ. Serine protease(s) secreted by Pezzulo AA, Tang XX, Hoegger MJ, Alaiwa MH, Ramachandran S, Moninger TO, et al. 870

785 the nematode Trichuris muris degrade the mucus barrier. PLoS Negl Trop Dis Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis 871

786 2012;6:e1856. lung. Nature 2012;487:109-13. 872

787 Henke MO, John G, Germann M, Lindemann H, Rubin BK. MUC5AC and MUC5B Puchelle E, Bajolet O, Abely M. Airway mucus in cystic fibrosis. Paediatr Respir Rev 873

788 mucins increase in cystic fibrosis airway secretions during pulmonary exacer- 2002;3:115-9. 874

789 bation. Am J Respir Crit Care Med 2007;175:816-21. Quinton PM. Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis. 875

790 Henke MO, John G, Rheineck C, Chillappagari S, Naehrlich L, Rubin BK Serine pro- Lancet 2008;372:415-7. 876

791 teases degrade airway mucins in cystic fibrosis. Infect Immun 2011;79:3438-44. Quinton PM. Role of epithelial HCO3(-) transport in mucin secretion: lessons from 877

792 Henke MO, Ratjen F. Mucolytics in cystic fibrosis. Paediatr Respir Rev 2007;8:24-9. cystic fibrosis. Am J Physiol Cell Physiol 2010;299:C1222-33. 878

793 Henke MO, Renner A, Huber RM, Seeds MC, Rubin BK. MUC5AC and MUC5B mucins Ramsey BW, Astley SJ, Aitken ML, Burke W, Colin AA, Dorkin HL, et al. Efficacy 879

794 are decreased in cystic fibrosis airway secretions. Am J Respir Cell Mol Biol and safety of short-term administration of aerosolized recombinant human 880

795 2004;31:86-91. deoxyribonuclease in patients with cystic fibrosis. Am Rev Respir Dis 1993;148: 881

796 Hong Z, Chasan B, Bansil R, Turner BS, Bhaskar KR, Afdhal NH. Atomic force 145-51. 882

797 microscopy reveals aggregation of gastric mucin at low pH. Biomacromolecules Ramsey BW, Davies J, McElvaney NG, Tullis E, Bell SC, Drevinek P, et al. A CFTR 883

798 2005;6:3458-66. potentiator in patients with cystic fibrosis and the G551D mutation. N Engl J 884

799 Horsley A, Rousseau K, Ridley C, Flight W, Jones A, Waigh TA, et al. Reassessment of Med 2011;365:1663-72. 885

800 the importance of mucins in determining sputum properties in cystic fibrosis. J Raynal BD, Hardingham TE, Sheehan JK, Thornton DJ. Calcium-dependent protein 886

801 Cyst Fibros 2013. interactions in MUC5B provide reversible cross-links in salivary mucus. J Biol 887

802 Innes AL, Carrington SD, Thornton DJ, Kirkham S, Rousseau K, Dougherty RH, et al. Chem 2003;278:28703-10. 888

803 Ex vivo sputum analysis reveals impairment of protease-dependent mucus Raynal BD, Hardingham TE, Thornton DJ, Sheehan JK. Concentrated solutions of 889

804 degradation by plasma proteins in acute asthma. Am J Respir Crit Care Med salivary MUC5B mucin do not replicate the gel-forming properties of saliva. 890

805 2009;180:203-10. Biochem J 2002;362:289-96. 891

806 Jones LC, Moussa L, Fulcher ML, Zhu Y, Hudson EJ, O'Neal WK, et al. VAMP8 is a ReidCJ, Hyde K, Ho SB, Harris A. Cystic fibrosis ofthe pancreas: involvement of MUC6 892

807 vesicle SNARE that regulates mucin secretion in airway goblet cells. J Physiol mucin in obstruction of pancreatic ducts. Mol Med 1997;3:403-11. 893

808 2012;590:545-62. Ridley C, Hughes GA, Bonser L, Ford RC, Thornton DJ. MUC5B mucin assembly and 894

809 Kesimer M, Ehre C, Burns KA, Davis CW, Sheehan JK, Pickles RJ. Molecular organi- extracellular organization. Pediatr Pulmonol 2011. 895

810 zation of the mucins and glycocalyx underlying mucus transport over mucosal RiordanJR, RommensJM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, et al. Identifica- 896

811 surfaces of the airways. Mucosal Immunol 2013;6:379-92. tion of the cystic fibrosis gene: cloning and characterization of complementary 897

812 Kesimer M, Makhov AM, Griffith JD, Verdugo P, SheehanJK. Unpacking agel-forming DNA. Science 1989;245:1066-73. 898

813 mucin: a view of MUC5B organization after granular release. Am J Physiol Lung Rogers CS, Stoltz DA, Meyerholz DK, Ostedgaard LS, Rokhlina T, Taft PJ, et al. Dis- 899

814 Cell Mol Physiol 2010;298:L15-22. ruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs. 900

815 Kirkham S, SheehanJK, Knight D, Richardson PS, Thornton DJ. Heterogeneity of air- Science 2008;321:1837-41. 901

816 ways mucus: variations in the amounts and glycoforms of the major oligomeric Rose MC, Brown CF, JacobyJZ3rd, Lynn WS, Kaufman B. Biochemical properties of 902

817 mucins MUC5AC and MUC5B. Biochem J 2002;361:537-46. tracheobronchial mucins from cystic fibrosis and non-cystic fibrosis individuals. 903

818 Knowles MR, Boucher RC. Mucus clearance as a primary innate defense mechanism Pediatr Res 1987;22:545-51. 904

819 for mammalian airways. J Clin Invest 2002;109:571-7. Rose MC, Voynow JA. Respiratory tract mucin genes and mucin glycoproteins in 905

820 Kreda SM, Davis CW, Rose MC. CFTR, mucins, and mucus obstruction in cystic fibrosis. health and disease. Physiol Rev 2006;86:245-78. 906

821 Cold Spring Harb Perspect Med 2012;2:a009589. Rosenbluth DB, Wilson K, Ferkol T, Schuster DP. Lung function decline in cystic fibro- 907

822 Kreda SM, Okada SF, van Heusden CA, O'Neal W, Gabriel S, Abdullah L, et al. Coor- sis patients and timing for lung transplantation referral. Chest 2004;126:412-9. 908

823 dinated release of nucleotides and mucin from human airway epithelial Calu-3 Round AN, Berry M, McMasterTJ, Corfield AP, Miles MJ. Glycopolymer charge density 909

824 cells. J Physiol 2007;584:245-59. determines conformation in humanocular mucingene products: an atomic force 910

825 Kreda SM, Seminario-Vidal L, van Heusden CA, O'Neal W, Jones L, Boucher RC, et al. microscope study. J Struct Biol 2004;145:246-53. 911

826 Receptor-promoted exocytosis of airway epithelial mucin granules containing Round AN, Rigby NM, Garcia de la Torre A, Macierzanka A, Mills EN, Mackie 912

827 a spectrum of adenine nucleotides. J Physiol 2010;588:2255-67. AR. Lamellar structures of MUC2-rich mucin: a potential role in governing 913

828 Kuver R, Lee SP. Calcium binding to biliary mucins is dependent on sodium ion the barrier and lubricating functions of intestinal mucus. Biomacromolecules 914

829 concentration: relevance to cystic fibrosis. Biochem Biophys Res Commun 2012;13:3253-61. 915

830 2004;314:330-4. Roy MG, Livraghi-Butrico A, Fletcher AA, McElwee MM, Evans SE, Boerner RM, et al. 916

831 Lethem MI, James SL, Marriott C, Burke JF. The origin of DNA associated with mucus Muc5b is required for airway defence. Nature 2013. 917

832 glycoproteins in cystic fibrosis sputum. Eur RespirJ 1990;3:19-23. Schachter H, Dixon GH. A comparative study ofthe proteins in normal meconium and 918

833 Lisowska A, Wojtowicz J, Walkowiak J. Small intestine bacterial overgrowth is fre- in meconium from meconium ileus patients. Can J Biochem 1965;43:381-97. 919

834 quent in cystic fibrosis: combined hydrogen and methane measurements are Shak S, Capon DJ, Hellmiss R, Marsters SA, Baker CL Recombinant human DNase 920

835 required for its detection. Acta Biochim Pol 2009;56:631-4. I reduces the viscosity of cystic fibrosis sputum. Proc Natl Acad Sci U S A 921

836 Livraghi-Butrico A, Kelly EJ, Klem ER, Dang H, Wolfgang MC, Boucher RC, et al. 1990;87:9188-92. 922

837 Mucus clearance, MyD88-dependent and MyD88-independent immunity mod- Sheehan JK Kirkham S, Howard M, Woodman P, Kutay S, Brazeau C, et al. Identifica- 923

838 ulate lung susceptibility to spontaneous bacterial infection and inflammation. tion of molecular intermediates in the assembly pathway of the MUC5AC mucin. 924

839 Mucosal Immunol 2012;5:397-408. J Biol Chem 2004;279:15698-705. 925

840 Lynch SV, Goldfarb KC, Wild YK, Kong W, De Lisle RC, Brodie EL. Cystic fibrosis Singer M, Martin LD, Vargaftig BB, Park J, Gruber AD, Li Y, et al. A MARCKS-related 926

841 transmembrane conductance regulator knockout mice exhibit aberrant gas- peptide blocks mucus hypersecretion in a mouse model of asthma. Nat Med 927

842 trointestinal microbiota. Gut Microbes 2013;4:41-7. 2004;10:193-6. 928

843 Mall M, Grubb BR, Harkema JR, O'Neal WK, Boucher RC. Increased airway epithe- Smith A. Pathogenesis of bacterial bronchitis in cystic fibrosis. Pediatr Infect Dis J 929

844 lial Na+ absorption produces cystic fibrosis-like lung disease in mice. Nat Med 1997;16:91-5 [discussion 5-6,123-6]. 930

845 2004;10:487-93. Snouwaert JN, Brigman KK, Latour AM, Malouf NN, Boucher RC, Smithies O, 931

846 Malmberg EK, Noaksson KA, Phillipson M, Johansson ME, Hinojosa-Kurtzberg M, et al. An animal model for cystic fibrosis made by gene targeting. Science 932

847 Holm L, et al. Increased levels of mucins in the cystic fibrosis mouse small 1992;257:1083-8. 933

848 intestine, and modulator effects of the Muc1 mucin expression. Am J Physiol Stoltz DA, Meyerholz DK, Pezzulo AA, Ramachandran S, Rogan MP, Davis GJ, et al. Cys- 934

849 Gastrointest Liver Physiol 2006;291:G203-10. tic fibrosis pigs develop lung disease and exhibit defective bacterial eradication 935

850 Matsui H, Randell SH, Peretti SW, Davis CW, Boucher RC. Coordinated clear- at birth. Sci Transl Med 2010;2:29ra31. 936

851 ance of periciliary liquid and mucus from airway surfaces. J Clin Invest Strong TV, Boehm K, Collins FS. Localization of cystic fibrosis transmembrane 937

852 1998;102:1125-31. conductance regulator mRNA in the human gastrointestinal tract by in situ 938

853 Matthews LW, Spector S, Lemm J, Potter JL. Studies on pulmonary secretions. I. The hybridization. J Clin Invest 1994;93:347-54. 939

854 over-all chemical composition of pulmonary secretions from patients with cystic Sun X, Sui H, Fisher JT, Yan Z, Liu X, Cho HJ, et al. Disease phenotype of a ferret 940

855 fibrosis, bronchiectasis, and laryngectomy. Am Rev Respir Dis 1963;88:199-204. CFTR-knockout model of cystic fibrosis. J Clin Invest 2010;120:3149-60. 941


10 C. Ehre et al. / The International Journal of Biochemistry & Cell Biology xxx (2014) xxx-xxx

942 Tam J, Nash EF, Ratjen F, Tullis E, Stephenson A. Nebulized and oral thiol deriva- Verdugo P. Mucus supramolecular topology: an elusive riddle. Proc Natl Acad Sci U 958

943 tives for pulmonary disease in cystic fibrosis. Cochrane Database Syst Rev S A 2012a;109:E2956 [author reply E7]. 959

944 2013;7:CD007168. Verdugo P. Supramolecular dynamics of mucus. Cold Spring Harb Perspect Med 960

945 Thornton DJ, Davies JR, Kraayenbrink M, Richardson PS, Sheehan JK, Carlstedt I. 2012b;2. 961

946 Mucus glycoproteins from 'normal' human tracheobronchial secretion. Biochem Verdugo P, Aitken M, Langley L, Villalon MJ. Molecular mechanism of product storage 962

947 J 1990;265:179-86. and release in mucin secretion. II. The role of extracellular Ca++. Biorheology 963

948 Thornton DJ, Rousseau K, McGuckin MA. Structure and function of the 1987;24:625-33. 964

949 polymeric mucins in airways mucus. Annu Rev Physiol 2008;70: Voynow JA, Rubin BK Mucins, mucus, and sputum. Chest 2009;135:505-12. 965

950 459-86. WannerA,SalatheM,O'RiordanTG.Mucociliaryclearanceintheairways.AmJRespir 966

951 Thornton DJ, Sheehan JK, Lindgren H, Carlstedt I. Mucus glycoproteins from cys- CritCare Med 1996;154:1868-902. 967

952 tic fibrotic sputum. Macromolecular properties and structural 'architecture'. Werlin SL, Benuri-Silbiger I, Kerem E, Adler SN, Goldin E, Zimmerman J, et al. 968

953 BiochemJ 1991;276(Pt 3):667-75. Evidence of intestinal inflammation in patients with cystic fibrosis. J Pediatr 969

954 Van Goor F, Hadida S, Grootenhuis PD, Burton B, Cao D, Neuberger T, et al. Rescue Gastroenterol Nutr 2010;51:304-8. 970

955 of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770. Proc Zhu Y, Ehre C, Abdullah LH, SheehanJK, Roy M, Evans CM, et al. Munc13-2-/- baseline 971

956 Natl Acad Sci U S A 2009;106:18825-30. secretion defect reveals source ofoligomeric mucins in mouse airways. J Physiol 972

957 Verdugo P. Mucin exocytosis. Am Rev Respir Dis 1991;144:S33-7. 2008;586:1977-92. 973