Cargando…

Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM

BACKGROUND: Caveolae are involved in diverse cellular functions such as signal transduction, cholesterol homeostasis, endo- and transcytosis, and also may serve as entry sites for microorganisms. Hence, their occurrence in epithelium of the airways might be expected but, nonetheless, has not yet bee...

Descripción completa

Detalles Bibliográficos
Autores principales: Krasteva, Gabriela, Pfeil, Uwe, Drab, Marek, Kummer, Wolfgang, König, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563466/
https://www.ncbi.nlm.nih.gov/pubmed/16904002
http://dx.doi.org/10.1186/1465-9921-7-108
_version_ 1782129511113949184
author Krasteva, Gabriela
Pfeil, Uwe
Drab, Marek
Kummer, Wolfgang
König, Peter
author_facet Krasteva, Gabriela
Pfeil, Uwe
Drab, Marek
Kummer, Wolfgang
König, Peter
author_sort Krasteva, Gabriela
collection PubMed
description BACKGROUND: Caveolae are involved in diverse cellular functions such as signal transduction, cholesterol homeostasis, endo- and transcytosis, and also may serve as entry sites for microorganisms. Hence, their occurrence in epithelium of the airways might be expected but, nonetheless, has not yet been examined. METHODS: Western blotting, real-time quantitative PCR analysis of abraded tracheal epithelium and laser-assisted microdissection combined with subsequent mRNA analysis were used to examine the expression of cav-1 and cav-2, two major caveolar coat proteins, in rat tracheal epithelium. Fluorescence immunohistochemistry was performed to locate caveolae and cav-1 and -2 in the airway epithelium of rats, mice and humans. Electron-microscopic analysis was used for the identification of caveolae. CLSM-FRET analysis determined the interaction of cav-1α and cav-2 in situ. RESULTS: Western blotting and laser-assisted microdissection identified protein and transcripts, respectively, of cav-1 and cav-2 in airway epithelium. Real-time quantitative RT-PCR analysis of abraded tracheal epithelium revealed a higher expression of cav-2 than of cav-1. Immunoreactivities for cav-1 and for cav-2 were co-localized in the cell membrane of the basal cells and basolaterally in the ciliated epithelial cells of large airways of rat and human. However, no labeling for cav-1 or cav-2 was observed in the epithelial cells of small bronchi. Using conventional double-labeling indirect immunofluorescence combined with CLSM-FRET analysis, we detected an association of cav-1α and -2 in epithelial cells. The presence of caveolae was confirmed by electron microscopy. In contrast to human and rat, cav-1-immunoreactivity and caveolae were confined to basal cells in mice. Epithelial caveolae were absent in cav-1-deficient mice, implicating a requirement of this caveolar protein in epithelial caveolae formation. CONCLUSION: These results show that caveolae and caveolins are integral membrane components in basal and ciliated epithelial cells, indicating a crucial role in these cell types. In addition to their physiological role, they may be involved in airway infection.
format Text
id pubmed-1563466
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-15634662006-09-09 Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM Krasteva, Gabriela Pfeil, Uwe Drab, Marek Kummer, Wolfgang König, Peter Respir Res Research BACKGROUND: Caveolae are involved in diverse cellular functions such as signal transduction, cholesterol homeostasis, endo- and transcytosis, and also may serve as entry sites for microorganisms. Hence, their occurrence in epithelium of the airways might be expected but, nonetheless, has not yet been examined. METHODS: Western blotting, real-time quantitative PCR analysis of abraded tracheal epithelium and laser-assisted microdissection combined with subsequent mRNA analysis were used to examine the expression of cav-1 and cav-2, two major caveolar coat proteins, in rat tracheal epithelium. Fluorescence immunohistochemistry was performed to locate caveolae and cav-1 and -2 in the airway epithelium of rats, mice and humans. Electron-microscopic analysis was used for the identification of caveolae. CLSM-FRET analysis determined the interaction of cav-1α and cav-2 in situ. RESULTS: Western blotting and laser-assisted microdissection identified protein and transcripts, respectively, of cav-1 and cav-2 in airway epithelium. Real-time quantitative RT-PCR analysis of abraded tracheal epithelium revealed a higher expression of cav-2 than of cav-1. Immunoreactivities for cav-1 and for cav-2 were co-localized in the cell membrane of the basal cells and basolaterally in the ciliated epithelial cells of large airways of rat and human. However, no labeling for cav-1 or cav-2 was observed in the epithelial cells of small bronchi. Using conventional double-labeling indirect immunofluorescence combined with CLSM-FRET analysis, we detected an association of cav-1α and -2 in epithelial cells. The presence of caveolae was confirmed by electron microscopy. In contrast to human and rat, cav-1-immunoreactivity and caveolae were confined to basal cells in mice. Epithelial caveolae were absent in cav-1-deficient mice, implicating a requirement of this caveolar protein in epithelial caveolae formation. CONCLUSION: These results show that caveolae and caveolins are integral membrane components in basal and ciliated epithelial cells, indicating a crucial role in these cell types. In addition to their physiological role, they may be involved in airway infection. BioMed Central 2006 2006-08-11 /pmc/articles/PMC1563466/ /pubmed/16904002 http://dx.doi.org/10.1186/1465-9921-7-108 Text en Copyright © 2006 Krasteva 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
Krasteva, Gabriela
Pfeil, Uwe
Drab, Marek
Kummer, Wolfgang
König, Peter
Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM
title Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM
title_full Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM
title_fullStr Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM
title_full_unstemmed Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM
title_short Caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by FRET-CLSM
title_sort caveolin-1 and -2 in airway epithelium: expression and in situ association as detected by fret-clsm
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563466/
https://www.ncbi.nlm.nih.gov/pubmed/16904002
http://dx.doi.org/10.1186/1465-9921-7-108
work_keys_str_mv AT krastevagabriela caveolin1and2inairwayepitheliumexpressionandinsituassociationasdetectedbyfretclsm
AT pfeiluwe caveolin1and2inairwayepitheliumexpressionandinsituassociationasdetectedbyfretclsm
AT drabmarek caveolin1and2inairwayepitheliumexpressionandinsituassociationasdetectedbyfretclsm
AT kummerwolfgang caveolin1and2inairwayepitheliumexpressionandinsituassociationasdetectedbyfretclsm
AT konigpeter caveolin1and2inairwayepitheliumexpressionandinsituassociationasdetectedbyfretclsm