Cholesterol-Regulated Stress Fiber Formation

被引:29
作者
Qi, Maosong [1 ]
Liu, Yuzhen [1 ]
Freeman, Michael R. [2 ,3 ,4 ]
Solomn, Keith R. [1 ,2 ,5 ]
机构
[1] Harvard Univ, Sch Med, Dept Orthopaed Surg, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Childrens Hosp, Dept Urol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Surg, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dept Orthopaed Surg, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
CHOLESTEROL; STRESS FIBER; RHO; ROCK; SRC; CAVEOLIN-1; SRC TYROSINE KINASES; SMOOTH-MUSCLE-CELLS; PLASMA-MEMBRANE; LIPID RAFTS; ACTIN CYTOSKELETON; C-SRC; CELLULAR CHOLESTEROL; OXIDATIVE-STRESS; FOCAL ADHESIONS; IN-VITRO;
D O I
10.1002/jcb.22081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dynamic interactions between cellular membranes and the cytoskeleton are known to play major roles in many cellular responses to environmental cues. External signals resulting in proliferation, differentiation, polarization, and motility must be translated from chemical signals into changes of state, often involving the cytoskeleton-dependent altering of cell shape and redistribution of molecules. Cholesterol, a critical component of eukaryotic cell membranes, performs vital roles in regulating membrane dynamics and function. Here we demonstrate, using mesenchymal and epithelial cell lines, that depletion of membrane cholesterol results in Src kinase-mediated Rho activation and caveolin phosphorylation, which together collaborate to form stress fibers. These results demonstrate that cholesterol is a critical regulator of membrane-cytoskeletal dynamics and suggest that altered cholesterol concentrations may result in dramatic changes in cellular responses mediated by the cytoskeleton. J. Cell. Biochem. 106: 1031-1040, 2009. (c) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1031 / 1040
页数:10
相关论文
共 66 条
[21]   DAP kinase mediates the phosphorylation of tropomyosin-1 downstream of the ERK pathway, which regulates the formation of stress fibers in response to oxidative stress [J].
Houle, Francois ;
Poirier, Andree ;
Dumaresq, Jeannot ;
Huot, Jacques .
JOURNAL OF CELL SCIENCE, 2007, 120 (20) :3666-3677
[22]  
Hughes-Fulford Millie, 2004, Sci STKE, V2004, pRE12
[23]   Cholesterol modulates the volume-regulated anion current in Ehrlich-Lettre ascites cells via effects on Rho and F-actin [J].
Klausen, Thomas Kjaer ;
Hougaard, Charlotte ;
Hoffmann, Else K. ;
Pedersen, Stine F. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 291 (04) :C757-C771
[24]   Membrane cholesterol, lateral mobility, and the phosphatidylinositol 4,5-bisphosphate-dependent organization of cell actin [J].
Kwik, J ;
Boyle, S ;
Fooksman, D ;
Margolis, L ;
Sheetz, MP ;
Edidin, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (24) :13964-13969
[25]   Src-mediated tyrosine phosphorylation of caveolin-1 induces its association with membrane type 1 matrix metalloproteinase [J].
Labrecque, L ;
Nyalendo, C ;
Langlois, S ;
Durocher, Y ;
Roghi, C ;
Murphy, G ;
Gingras, D ;
Béliveau, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (50) :52132-52140
[26]   Caveolin-1 mutations (P132L and null) and the pathogenesis of breast cancer - Caveolin-1 (P132L) behaves in a dominant-negative manner and Caveolin-1 (-/-) null mice show mammary epithelial cell hyperplasia [J].
Lee, H ;
Park, DS ;
Razani, B ;
Russell, RG ;
Pestell, RG ;
Lisanti, MP .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (04) :1357-1369
[27]   Constitutive and growth factor-regulated phosphorylation of caveolin-1 occurs at the same site (Tyr-14) in vivo:: Identification of a c-Src/Cav-1/Grb7 signaling cassette [J].
Lee, H ;
Volonte, D ;
Galbiati, F ;
Iyengar, P ;
Lublin, DM ;
Bregman, DB ;
Wilson, MT ;
Campos-Gonzalez, R ;
Bouzahzah, B ;
Pestell, RG ;
Scherer, PE ;
Lisanti, MP .
MOLECULAR ENDOCRINOLOGY, 2000, 14 (11) :1750-1775
[28]  
Leitinger B, 2002, J CELL SCI, V115, P963
[29]   Src tyrosine kinases, G(alpha) subunits, and H-Ras share a common membrane-anchored scaffolding protein, caveolin - Caveolin binding negatively regulates the auto-activation of Src tyrosine kinases [J].
Li, SW ;
Couet, J ;
Lisanti, MP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (46) :29182-29190
[30]  
Li SW, 1996, J BIOL CHEM, V271, P3863