Regulated Mucin Secretion from Airway Epithelial Cells

Secretory epithelial cells of the proximal airways synthesize and secrete gel-forming polymeric mucins. The secreted mucins adsorb water to form mucus that is propelled by neighboring ciliated cells, providing a mobile barrier which removes inhaled particles and pathogens from the lungs. Several fea...

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Main Authors: Kenneth Bruce Adler, Michael J. Tuvim, Burton F Dickey
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-09-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fendo.2013.00129/full
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author Kenneth Bruce Adler
Michael J. Tuvim
Burton F Dickey
author_facet Kenneth Bruce Adler
Michael J. Tuvim
Burton F Dickey
author_sort Kenneth Bruce Adler
collection DOAJ
description Secretory epithelial cells of the proximal airways synthesize and secrete gel-forming polymeric mucins. The secreted mucins adsorb water to form mucus that is propelled by neighboring ciliated cells, providing a mobile barrier which removes inhaled particles and pathogens from the lungs. Several features of the intracellular trafficking of mucins make the airway secretory cell an interesting comparator for the cell biology of regulated exocytosis. Polymeric mucins are exceedingly large molecules (up to 3x10^6 D per monomer) whose folding and initial polymerization in the ER requires the protein disulfide isomerase Agr2. In the Golgi, mucins further polymerize to form chains and possibly branched networks comprising more than 20 monomers. The large size of mucin polymers imposes constraints on their packaging into transport vesicles along the secretory pathway. Sugar side chains account for >70% of the mass of mucins, and their attachment to the protein core by O-glycosylation occurs in the Golgi. Mature polymeric mucins are stored in large secretory granules ~1 um in diameter. These are translocated to the apical membrane to be positioned for exocytosis by cooperative interactions among MARCKS, cysteine string protein (CSP), HSP70 and the cytoskeleton. Mucin granules undergo exocytic fusion with the plasma membrane at a low basal rate and a high stimulated rate. Both rates are mediated by a regulated exocytic mechanism as indicated by phenotypes in both basal and stimulated secretion in mice lacking Munc13-2, a sensor of the second messengers calcium and diacylglycerol (DAG). Basal secretion is induced by low levels of activation of P2Y2 purinergic and A3 adenosine receptors by extracellular ATP released in paracrine fashion and its metabolite adenosine. Stimulated secretion is induced by high levels of the same ligands, and possibly by inflammatory mediators as well. Activated receptors are coupled to phospholipase C by Gq, resulting in the generation of DAG and of
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spelling doaj.art-ad475be187d541958ba78ec30fa4cc8a2022-12-22T03:40:19ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922013-09-01410.3389/fendo.2013.0012958171Regulated Mucin Secretion from Airway Epithelial CellsKenneth Bruce Adler0Michael J. Tuvim1Burton F Dickey2North Carolina State UniversityUniversity of Texas MD Anderson Cancer CenterUniversity of Texas MD Anderson Cancer CenterSecretory epithelial cells of the proximal airways synthesize and secrete gel-forming polymeric mucins. The secreted mucins adsorb water to form mucus that is propelled by neighboring ciliated cells, providing a mobile barrier which removes inhaled particles and pathogens from the lungs. Several features of the intracellular trafficking of mucins make the airway secretory cell an interesting comparator for the cell biology of regulated exocytosis. Polymeric mucins are exceedingly large molecules (up to 3x10^6 D per monomer) whose folding and initial polymerization in the ER requires the protein disulfide isomerase Agr2. In the Golgi, mucins further polymerize to form chains and possibly branched networks comprising more than 20 monomers. The large size of mucin polymers imposes constraints on their packaging into transport vesicles along the secretory pathway. Sugar side chains account for >70% of the mass of mucins, and their attachment to the protein core by O-glycosylation occurs in the Golgi. Mature polymeric mucins are stored in large secretory granules ~1 um in diameter. These are translocated to the apical membrane to be positioned for exocytosis by cooperative interactions among MARCKS, cysteine string protein (CSP), HSP70 and the cytoskeleton. Mucin granules undergo exocytic fusion with the plasma membrane at a low basal rate and a high stimulated rate. Both rates are mediated by a regulated exocytic mechanism as indicated by phenotypes in both basal and stimulated secretion in mice lacking Munc13-2, a sensor of the second messengers calcium and diacylglycerol (DAG). Basal secretion is induced by low levels of activation of P2Y2 purinergic and A3 adenosine receptors by extracellular ATP released in paracrine fashion and its metabolite adenosine. Stimulated secretion is induced by high levels of the same ligands, and possibly by inflammatory mediators as well. Activated receptors are coupled to phospholipase C by Gq, resulting in the generation of DAG and ofhttp://journal.frontiersin.org/Journal/10.3389/fendo.2013.00129/fullExocytosisMucussecretionmucinsynaptotagminMARCKS
spellingShingle Kenneth Bruce Adler
Michael J. Tuvim
Burton F Dickey
Regulated Mucin Secretion from Airway Epithelial Cells
Frontiers in Endocrinology
Exocytosis
Mucus
secretion
mucin
synaptotagmin
MARCKS
title Regulated Mucin Secretion from Airway Epithelial Cells
title_full Regulated Mucin Secretion from Airway Epithelial Cells
title_fullStr Regulated Mucin Secretion from Airway Epithelial Cells
title_full_unstemmed Regulated Mucin Secretion from Airway Epithelial Cells
title_short Regulated Mucin Secretion from Airway Epithelial Cells
title_sort regulated mucin secretion from airway epithelial cells
topic Exocytosis
Mucus
secretion
mucin
synaptotagmin
MARCKS
url http://journal.frontiersin.org/Journal/10.3389/fendo.2013.00129/full
work_keys_str_mv AT kennethbruceadler regulatedmucinsecretionfromairwayepithelialcells
AT michaeljtuvim regulatedmucinsecretionfromairwayepithelialcells
AT burtonfdickey regulatedmucinsecretionfromairwayepithelialcells