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Clara cell adhesion and migration to extracellular matrix

BACKGROUND: Clara cells are the epithelial progenitor cell of the small airways, a location known to be important in many lung disorders. Although migration of alveolar type II and bronchiolar ciliated epithelial cells has been examined, the migratory response of Clara cells has received little atte...

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Autores principales: Atkinson, Jeffrey J, Adair-Kirk, Tracy L, Kelley, Diane G, deMello, Daphne, Senior, Robert M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2249579/
https://www.ncbi.nlm.nih.gov/pubmed/18179694
http://dx.doi.org/10.1186/1465-9921-9-1
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author Atkinson, Jeffrey J
Adair-Kirk, Tracy L
Kelley, Diane G
deMello, Daphne
Senior, Robert M
author_facet Atkinson, Jeffrey J
Adair-Kirk, Tracy L
Kelley, Diane G
deMello, Daphne
Senior, Robert M
author_sort Atkinson, Jeffrey J
collection PubMed
description BACKGROUND: Clara cells are the epithelial progenitor cell of the small airways, a location known to be important in many lung disorders. Although migration of alveolar type II and bronchiolar ciliated epithelial cells has been examined, the migratory response of Clara cells has received little attention. METHODS: Using a modification of existing procedures for Clara cell isolation, we examined mouse Clara cells and a mouse Clara-like cell line (C22) for adhesion to and migration toward matrix substrate gradients, to establish the nature and integrin dependence of migration in Clara cells. RESULTS: We observed that Clara cells adhere preferentially to fibronectin (Fn) and type I collagen (Col I) similar to previous reports. Migration of Clara cells can be directed by a fixed gradient of matrix substrates (haptotaxis). Migration of the C22 cell line was similar to the Clara cells so integrin dependence of migration was evaluated with this cell line. As determined by competition with an RGD containing-peptide, migration of C22 cells toward Fn and laminin (Lm) 511 (formerly laminin 10) was significantly RGD integrin dependent, but migration toward Col I was RGD integrin independent, suggesting that Clara cells utilize different receptors for these different matrices. CONCLUSION: Thus, Clara cells resemble alveolar type II and bronchiolar ciliated epithelial cells by showing integrin mediated pro-migratory changes to extracellular matrix components that are present in tissues after injury.
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spelling pubmed-22495792008-02-22 Clara cell adhesion and migration to extracellular matrix Atkinson, Jeffrey J Adair-Kirk, Tracy L Kelley, Diane G deMello, Daphne Senior, Robert M Respir Res Research BACKGROUND: Clara cells are the epithelial progenitor cell of the small airways, a location known to be important in many lung disorders. Although migration of alveolar type II and bronchiolar ciliated epithelial cells has been examined, the migratory response of Clara cells has received little attention. METHODS: Using a modification of existing procedures for Clara cell isolation, we examined mouse Clara cells and a mouse Clara-like cell line (C22) for adhesion to and migration toward matrix substrate gradients, to establish the nature and integrin dependence of migration in Clara cells. RESULTS: We observed that Clara cells adhere preferentially to fibronectin (Fn) and type I collagen (Col I) similar to previous reports. Migration of Clara cells can be directed by a fixed gradient of matrix substrates (haptotaxis). Migration of the C22 cell line was similar to the Clara cells so integrin dependence of migration was evaluated with this cell line. As determined by competition with an RGD containing-peptide, migration of C22 cells toward Fn and laminin (Lm) 511 (formerly laminin 10) was significantly RGD integrin dependent, but migration toward Col I was RGD integrin independent, suggesting that Clara cells utilize different receptors for these different matrices. CONCLUSION: Thus, Clara cells resemble alveolar type II and bronchiolar ciliated epithelial cells by showing integrin mediated pro-migratory changes to extracellular matrix components that are present in tissues after injury. BioMed Central 2008 2008-01-07 /pmc/articles/PMC2249579/ /pubmed/18179694 http://dx.doi.org/10.1186/1465-9921-9-1 Text en Copyright © 2008 Atkinson 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
Atkinson, Jeffrey J
Adair-Kirk, Tracy L
Kelley, Diane G
deMello, Daphne
Senior, Robert M
Clara cell adhesion and migration to extracellular matrix
title Clara cell adhesion and migration to extracellular matrix
title_full Clara cell adhesion and migration to extracellular matrix
title_fullStr Clara cell adhesion and migration to extracellular matrix
title_full_unstemmed Clara cell adhesion and migration to extracellular matrix
title_short Clara cell adhesion and migration to extracellular matrix
title_sort clara cell adhesion and migration to extracellular matrix
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2249579/
https://www.ncbi.nlm.nih.gov/pubmed/18179694
http://dx.doi.org/10.1186/1465-9921-9-1
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