Molecular dissection of PINCH-1 reveals a mechanism of coupling and uncoupling of cell shape modulation and survival

被引:33
作者
Xu, Z
Fukuda, T
Li, Y
Zha, XL
Qin, J
Wu, CY
机构
[1] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA 15261 USA
[2] Fudan Univ, Shanghai Med Coll, Dept Biochem & Mol Biol, Shanghai 200032, Peoples R China
[3] Cleveland Clin Fdn, Lerner Res Inst, Struct Biol Program, Cleveland, OH 44195 USA
关键词
D O I
10.1074/jbc.M504189200
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
How cells couple and uncouple regulation of cellular processes such as shape change and survival is an important question in molecular cell biology. PINCH-1, a widely expressed protein consisting of five LIM domains and a C-terminal tail, is an essential focal adhesion protein with multiple functions including regulation of the integrin-linked kinase ( ILK) level, cell shape, and survival signaling. We show here that the LIM1-mediated interaction with ILK regulates all these three processes. By contrast, the LIM4-mediated interaction with Nck-2, which regulates cell morphology and migration, is not required for the control of the ILK level and survival. Remarkably, a short 15-residue tail C-terminal to LIM5 is required for both cell shape modulation and survival, albeit it is not required for the control of the ILK level. The C-terminal tail not only regulates PINCH-1 localization to focal adhesions but also functions after it localizes there. These findings suggest that PINCH-1 functions as a molecular platform for coupling and uncoupling diverse cellular processes via overlapping but yet distinct domain interactions.
引用
收藏
页码:27631 / 27637
页数:7
相关论文
共 42 条
[1]   The murine Nck SH2/SH3 adaptors are important for the development of mesoderm-derived embryonic structures and for regulating the cellular actin network [J].
Bladt, F ;
Aippersbach, E ;
Gelkop, S ;
Strasser, GA ;
Nash, P ;
Tafuri, A ;
Gertler, FB ;
Pawson, T .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (13) :4586-4597
[2]   Thymosin β4 activates integrin-linked kinase and promotes cardiac cell migration, survival and cardiac repair [J].
Bock-Marquette, I ;
Saxena, A ;
White, MD ;
DiMaio, JM ;
Srivastava, D .
NATURE, 2004, 432 (7016) :466-472
[3]   PINCH2 is a new five LIM domain protein, homologous to PINCH and localized to focal adhesions [J].
Braun, A ;
Bordoy, R ;
Stanchi, F ;
Moser, M ;
Kostka, G ;
Ehler, E ;
Brandau, O ;
Fässler, R .
EXPERIMENTAL CELL RESEARCH, 2003, 284 (02) :239-250
[4]   The Nck family of adapter proteins:: Regulators of actin cytoskeleton [J].
Buday, L ;
Wunderlich, L ;
Tamás, P .
CELLULAR SIGNALLING, 2002, 14 (09) :723-731
[5]   Identification of PINCH in Schwann cells and DRG neurons: Shuttling and signaling after nerve injury [J].
Campana, WM ;
Myers, RR ;
Rearden, A .
GLIA, 2003, 41 (03) :213-223
[6]   Analysis of PINCH function in Drosophila demonstrates its requirement in integrin-dependent cellular processes [J].
Clark, KA ;
McGrail, M ;
Beckerle, MC .
DEVELOPMENT, 2003, 130 (12) :2611-2621
[7]   Cell-substrate interactions and signaling through ILK [J].
Dedhar, S .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (02) :250-256
[8]   Integrin-linked kinase (ILK): a regulator of integrin and growth-factor signalling [J].
Dedhar, S ;
Williams, B ;
Hannigan, G .
TRENDS IN CELL BIOLOGY, 1999, 9 (08) :319-323
[9]   Integrin signaling to the actin cytoskeleton [J].
DeMali, KA ;
Wennerberg, K ;
Burridge, K .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (05) :572-582
[10]   The Ras suppressor Rsu-1 binds to the LIM 5 domain of the adaptor protein PINCH1 and participates in adhesion-related functions [J].
Dougherty, GW ;
Chopp, T ;
Qi, S ;
Cutler, ML .
EXPERIMENTAL CELL RESEARCH, 2005, 306 (01) :168-179