Cargando…

Caveolin-1, cellular senescence and pulmonary emphysema

Caveolae are vesicular invaginations of the plasma membrane. Caveolin-1 is the structural protein component of caveolae. Caveolin-1 participates in signal transduction processes by acting as a scaffolding protein that concentrates, organizes and functional regulates signaling molecules within caveol...

Descripción completa

Detalles Bibliográficos
Autores principales: Volonte, Daniela, Galbiati, Ferruccio
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2815740/
https://www.ncbi.nlm.nih.gov/pubmed/20157570
_version_ 1782177036180127744
author Volonte, Daniela
Galbiati, Ferruccio
author_facet Volonte, Daniela
Galbiati, Ferruccio
author_sort Volonte, Daniela
collection PubMed
description Caveolae are vesicular invaginations of the plasma membrane. Caveolin-1 is the structural protein component of caveolae. Caveolin-1 participates in signal transduction processes by acting as a scaffolding protein that concentrates, organizes and functional regulates signaling molecules within caveolar membranes. Cigarette smoke, a source of oxidants, is an environmental hazard that causes pulmonary emphysema. Recently, we reported that the development of cigarette smoking-induced pulmonary emphysema was inhibited in caveolin-1 null mice, which do not express caveolin-1. We demonstrated that lack of caveolin-1 expression in lung fibroblasts dramatically inhibited premature senescence induced by oxidants contained in cigarette smoke. Mechanistically, we uncovered that premature senescence of lung fibroblasts induced by oxidative stress occurred through activation of an ataxia telangiectasia-mutated (ATM)/p53-depedent pathway following sequestration of the catalytic subunit of protein phosphatase 2A (PP2A-C), an inhibitor of ATM, by caveolin-1 into caveolar membranes. We propose caveolin-1 as a key player of a novel signaling pathway that links cigarette smoke to premature senescence of lung fibroblasts and development of pulmonary emphysema.
format Text
id pubmed-2815740
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-28157402010-02-12 Caveolin-1, cellular senescence and pulmonary emphysema Volonte, Daniela Galbiati, Ferruccio Aging (Albany NY) Research Perspective Caveolae are vesicular invaginations of the plasma membrane. Caveolin-1 is the structural protein component of caveolae. Caveolin-1 participates in signal transduction processes by acting as a scaffolding protein that concentrates, organizes and functional regulates signaling molecules within caveolar membranes. Cigarette smoke, a source of oxidants, is an environmental hazard that causes pulmonary emphysema. Recently, we reported that the development of cigarette smoking-induced pulmonary emphysema was inhibited in caveolin-1 null mice, which do not express caveolin-1. We demonstrated that lack of caveolin-1 expression in lung fibroblasts dramatically inhibited premature senescence induced by oxidants contained in cigarette smoke. Mechanistically, we uncovered that premature senescence of lung fibroblasts induced by oxidative stress occurred through activation of an ataxia telangiectasia-mutated (ATM)/p53-depedent pathway following sequestration of the catalytic subunit of protein phosphatase 2A (PP2A-C), an inhibitor of ATM, by caveolin-1 into caveolar membranes. We propose caveolin-1 as a key player of a novel signaling pathway that links cigarette smoke to premature senescence of lung fibroblasts and development of pulmonary emphysema. Impact Journals LLC 2009-08-10 /pmc/articles/PMC2815740/ /pubmed/20157570 Text en Copyright: ©2009 Volonte et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Perspective
Volonte, Daniela
Galbiati, Ferruccio
Caveolin-1, cellular senescence and pulmonary emphysema
title Caveolin-1, cellular senescence and pulmonary emphysema
title_full Caveolin-1, cellular senescence and pulmonary emphysema
title_fullStr Caveolin-1, cellular senescence and pulmonary emphysema
title_full_unstemmed Caveolin-1, cellular senescence and pulmonary emphysema
title_short Caveolin-1, cellular senescence and pulmonary emphysema
title_sort caveolin-1, cellular senescence and pulmonary emphysema
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2815740/
https://www.ncbi.nlm.nih.gov/pubmed/20157570
work_keys_str_mv AT volontedaniela caveolin1cellularsenescenceandpulmonaryemphysema
AT galbiatiferruccio caveolin1cellularsenescenceandpulmonaryemphysema