Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1782213051563376640 |
---|---|
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." |
format | Online Article Text |
id | pubmed-3184067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT raifordkimberlyl mucingranuleassociatedproteinsinhumanbronchialepithelialcellstheairwaygobletcellgranulome AT parkjoungjoa mucingranuleassociatedproteinsinhumanbronchialepithelialcellstheairwaygobletcellgranulome AT linkowei mucingranuleassociatedproteinsinhumanbronchialepithelialcellstheairwaygobletcellgranulome AT fangshijing mucingranuleassociatedproteinsinhumanbronchialepithelialcellstheairwaygobletcellgranulome AT crewsannel mucingranuleassociatedproteinsinhumanbronchialepithelialcellstheairwaygobletcellgranulome AT adlerkennethb mucingranuleassociatedproteinsinhumanbronchialepithelialcellstheairwaygobletcellgranulome |