Caveolin-1, cellular senescence and pulmonary emphysema

被引:33
作者
Volonte, Daniela [1 ]
Galbiati, Ferruccio [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15261 USA
来源
AGING-US | 2009年 / 1卷 / 09期
关键词
Caveolin; oxidative stress; premature senescence; p53; INDUCED PREMATURE SENESCENCE; LUNG FIBROBLASTS; GROWTH ARREST; CELLS; EXPRESSION; CULTURE; GENES; G(1); SHOW;
D O I
10.18632/aging.100079
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:831 / 835
页数:5
相关论文
共 36 条
  • [1] BARTHOLOMEW JN, 2009, CANC RES IN PRESS
  • [2] Transient deactivation of ERK signalling is sufficient for stable entry into G0 in primary avian fibroblasts
    Black, EJ
    Clark, W
    Gillespie, DAF
    [J]. CURRENT BIOLOGY, 2000, 10 (18) : 1119 - 1122
  • [3] Inflamm-aging: autoimmunity, and the immune-risk phenotype
    Boren, E
    Gershwin, ME
    [J]. AUTOIMMUNITY REVIEWS, 2004, 3 (05) : 401 - 406
  • [4] Senescent cells, tumor suppression, and organismal aging: Good citizens, bad neighbors
    Campisi, J
    [J]. CELL, 2005, 120 (04) : 513 - 522
  • [5] SENESCENCE-LIKE GROWTH ARREST INDUCED BY HYDROGEN-PEROXIDE IN HUMAN-DIPLOID FIBROBLAST F65 CELLS
    CHEN, Q
    AMES, BN
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) : 4130 - 4134
  • [6] Chen QM, 2000, ANN NY ACAD SCI, V908, P111
  • [7] Molecular analysis of H2O2-induced senescent-like growth arrest in normal human fibroblasts:: p53 and Rb control G1 arrest but not cell replication
    Chen, QM
    Bartholomew, JC
    Campisi, J
    Acosta, M
    Reagan, JD
    Ames, BN
    [J]. BIOCHEMICAL JOURNAL, 1998, 332 : 43 - 50
  • [8] Morphological adjustment of senescent cells by modulating caveolin-1 status
    Cho, KA
    Ryu, SJ
    Oh, YS
    Park, JH
    Lee, JW
    Kim, HP
    Kim, KT
    Jang, IS
    Park, SC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (40) : 42270 - 42278
  • [9] Senescent phenotype can be reversed by reduction of caveolin status
    Cho, KA
    Ryu, SJ
    Park, JS
    Jang, IS
    Ahn, JS
    Kim, KT
    Park, SC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (30) : 27789 - 27795
  • [10] Molecular inflammation hypothesis of aging based on the anti-aging mechanism of calorie restriction
    Chung, HY
    Kim, HJ
    Kim, KW
    Choi, JS
    Yu, BP
    [J]. MICROSCOPY RESEARCH AND TECHNIQUE, 2002, 59 (04) : 264 - 272