Focal adhesions - Paradigm for a signaling nexus

被引:204
作者
Romer, LH
Birukov, KG
Garcia, JGN
机构
[1] Johns Hopkins Univ, Sch Med, Dept Anesthesiol & Crit Care Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Dept Cell Biol, Baltimore, MD 21287 USA
[4] Univ Chicago, Dept Med, Chicago, IL 60637 USA
关键词
cell adhesion; extracellular matrix; integrin; mechanical force; cell signaling; focal adhesion; vascular endothelium; vascular smooth muscle;
D O I
10.1161/01.RES.0000207408.31270.db
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The vascular wall contains intimal endothelium and medial smooth muscle that act as contiguous tissues with tight spatial and functional coordination in response to tonic and episodic input from the bloodstream and the surrounding parenchyma. Focal adhesions are molecular bridges between the intracellular and extracellular spaces that integrate a variety of environmental stimuli and mediate 2-way crosstalk between the extracellular matrix and the cytoskeleton. Focal adhesion components are targets for biochemical and mechanical stimuli that evoke crucial developmental and injury response mechanisms including cell growth, movement, and differentiation, and tailoring of the extracellular microenvironment. Focal adhesions provide the vascular wall constituents with flexible and specific tools for exchanging cues in a complex system. The molecular mechanisms that underlie these vital communications are detailed in this review with the goal of defining future targets for vascular tissue engineering and for the therapeutic modulation of disordered vascular growth, inflammation, thrombosis, and angiogenesis.
引用
收藏
页码:606 / 616
页数:11
相关论文
共 148 条
[61]  
INGBER DE, 1979, ANNU REV PHYSIOL, V59, P575
[62]   Vinculin activation by talin through helical bundle conversion [J].
Izard, T ;
Evans, G ;
Borgon, RA ;
Rush, CL ;
Bricogne, G ;
Bois, PRJ .
NATURE, 2004, 427 (6970) :171-175
[63]   Cytoskeletal activation and altered gene expression in endothelial barrier regulation by simvastatin [J].
Jacobson, JR ;
Dudek, SM ;
Birukov, KG ;
Ye, SQ ;
Grigoryev, DN ;
Girgis, RE ;
Garcia, JGN .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2004, 30 (05) :662-670
[64]   Integrin activation and matrix binding mediate cellular responses to mechanical stretch [J].
Katsumi, A ;
Naoe, T ;
Matsushita, T ;
Kaibuchi, K ;
Schwartz, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) :16546-16549
[65]   Targeting membrane-localized focal adhesion kinase to focal adhesions - Roles of tyrosine phosphorylation and Src family kinases [J].
Katz, BZ ;
Romer, L ;
Miyamoto, S ;
Volberg, T ;
Matsumoto, K ;
Cukierman, E ;
Geiger, B ;
Yamada, KM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (31) :29115-29120
[66]   Physical state of the extracellular matrix regulates the structure and molecular composition of cell-matrix adhesions [J].
Katz, BZ ;
Zamir, E ;
Bershadsky, A ;
Kam, Z ;
Yamada, KM ;
Geiger, B .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (03) :1047-1060
[67]   Processive capping by formin suggests a force-driven mechanism of actin polymerization [J].
Kozlov, MM ;
Bershadsky, AD .
JOURNAL OF CELL BIOLOGY, 2004, 167 (06) :1011-1017
[68]   Forced unfolding of the fibronectin type III module reveals a tensile molecular recognition switch [J].
Krammer, A ;
Lu, H ;
Isralewitz, B ;
Schulten, K ;
Vogel, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1351-1356
[69]   Focal adhesion kinase suppresses apoptosis by binding to the death domain of receptor-interacting protein [J].
Kurenova, E ;
Xu, LH ;
Yang, XH ;
Baldwin, AS ;
Craven, RJ ;
Hanks, SK ;
Liu, ZG ;
Cance, WG .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (10) :4361-4371
[70]   ADAM12 and α9β1 integrin are instrumental in human myogenic cell differentiation [J].
Lafuste, P ;
Sonnet, C ;
Chazaud, B ;
Dreyfus, PA ;
Gherardi, RK ;
Wewer, UM ;
Authier, FJ .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (02) :861-870