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Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"

BACKGROUND: Excess mucus in the airways leads to obstruction in diseases such as chronic bronchitis, asthma, and cystic fibrosis. Mucins, the highly glycosolated protein components of mucus, are stored in membrane-bound granules housed in the cytoplasm of airway epithelial "goblet" cells u...

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Autores principales: Raiford, Kimberly L, Park, Joungjoa, Lin, Ko-Wei, Fang, Shijing, Crews, Anne L, Adler, Kenneth B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184067/
https://www.ncbi.nlm.nih.gov/pubmed/21896166
http://dx.doi.org/10.1186/1465-9921-12-118
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author Raiford, Kimberly L
Park, Joungjoa
Lin, Ko-Wei
Fang, Shijing
Crews, Anne L
Adler, Kenneth B
author_facet Raiford, Kimberly L
Park, Joungjoa
Lin, Ko-Wei
Fang, Shijing
Crews, Anne L
Adler, Kenneth B
author_sort Raiford, Kimberly L
collection PubMed
description BACKGROUND: Excess mucus in the airways leads to obstruction in diseases such as chronic bronchitis, asthma, and cystic fibrosis. Mucins, the highly glycosolated protein components of mucus, are stored in membrane-bound granules housed in the cytoplasm of airway epithelial "goblet" cells until they are secreted into the airway lumen via an exocytotic process. Precise mechanism(s) of mucin secretion, including the specific proteins involved in the process, have yet to be elucidated. Previously, we have shown that the Myristoylated Alanine-Rich C Kinase Substrate (MARCKS) protein regulates mucin secretion by orchestrating translocation of mucin granules from the cytosol to the plasma membrane, where the granules dock, fuse and release their contents into the airway lumen. Associated with MARCKS in this process are chaperone (Heat Shock Protein 70 [HSP70], Cysteine string protein [CSP]) and cytoskeletal (actin, myosin) proteins. However, additional granule-associated proteins that may be involved in secretion have not yet been elucidated. METHODS: Here, we isolated mucin granules and granule membranes from primary cultures of well differentiated human bronchial epithelial cells utilizing a novel technique of immuno-isolation, based on the presence of the calcium activated chloride channel hCLCA1 (the human ortholog of murine Gob-5) on the granule membranes, and verified via Western blotting and co-immunoprecipitation that MARCKS, HSP70, CSP and hCLCA1 were present on the granule membranes and associated with each other. We then subjected the isolated granules/membranes to liquid chromatography mass spectrometry (LC-MS/MS) to identify other granule associated proteins. RESULTS: A number of additional cytoskeletal (e.g. Myosin Vc) and regulatory proteins (e.g. Protein phosphatase 4) associated with the granules and could play a role in secretion were discovered. This is the first description of the airway goblet cell "granulome."
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spelling pubmed-31840672011-10-01 Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome" Raiford, Kimberly L Park, Joungjoa Lin, Ko-Wei Fang, Shijing Crews, Anne L Adler, Kenneth B Respir Res Research BACKGROUND: Excess mucus in the airways leads to obstruction in diseases such as chronic bronchitis, asthma, and cystic fibrosis. Mucins, the highly glycosolated protein components of mucus, are stored in membrane-bound granules housed in the cytoplasm of airway epithelial "goblet" cells until they are secreted into the airway lumen via an exocytotic process. Precise mechanism(s) of mucin secretion, including the specific proteins involved in the process, have yet to be elucidated. Previously, we have shown that the Myristoylated Alanine-Rich C Kinase Substrate (MARCKS) protein regulates mucin secretion by orchestrating translocation of mucin granules from the cytosol to the plasma membrane, where the granules dock, fuse and release their contents into the airway lumen. Associated with MARCKS in this process are chaperone (Heat Shock Protein 70 [HSP70], Cysteine string protein [CSP]) and cytoskeletal (actin, myosin) proteins. However, additional granule-associated proteins that may be involved in secretion have not yet been elucidated. METHODS: Here, we isolated mucin granules and granule membranes from primary cultures of well differentiated human bronchial epithelial cells utilizing a novel technique of immuno-isolation, based on the presence of the calcium activated chloride channel hCLCA1 (the human ortholog of murine Gob-5) on the granule membranes, and verified via Western blotting and co-immunoprecipitation that MARCKS, HSP70, CSP and hCLCA1 were present on the granule membranes and associated with each other. We then subjected the isolated granules/membranes to liquid chromatography mass spectrometry (LC-MS/MS) to identify other granule associated proteins. RESULTS: A number of additional cytoskeletal (e.g. Myosin Vc) and regulatory proteins (e.g. Protein phosphatase 4) associated with the granules and could play a role in secretion were discovered. This is the first description of the airway goblet cell "granulome." BioMed Central 2011 2011-09-06 /pmc/articles/PMC3184067/ /pubmed/21896166 http://dx.doi.org/10.1186/1465-9921-12-118 Text en Copyright ©2011 Raiford et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Raiford, Kimberly L
Park, Joungjoa
Lin, Ko-Wei
Fang, Shijing
Crews, Anne L
Adler, Kenneth B
Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"
title Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"
title_full Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"
title_fullStr Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"
title_full_unstemmed Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"
title_short Mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"
title_sort mucin granule-associated proteins in human bronchial epithelial cells: the airway goblet cell "granulome"
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184067/
https://www.ncbi.nlm.nih.gov/pubmed/21896166
http://dx.doi.org/10.1186/1465-9921-12-118
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