Endothelial extracellular matrix - Biosynthesis, remodeling, and functions during vascular morphogenesis and neovessel stabilization

被引:929
作者
Davis, GE
Senger, DR
机构
[1] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[2] Texas A&M Univ, Syst Hlth Sci Ctr, Dept Pathol, College Stn, TX 77843 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
extracellular matrix; endothelial cells; angiogenesis; vascular morphogenesis; vessel stabilization;
D O I
10.1161/01.RES.0000191547.64391.e3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The extracellular matrix (ECM) is critical for all aspects of vascular biology. In concert with supporting cells, endothelial cells (ECs) assemble a laminin- rich basement membrane matrix that provides structural and organizational stability. During the onset of angiogenesis, this basement membrane matrix is degraded by proteinases, among which membrane-type matrix metalloproteinases (MT-MMPs) are particularly significant. As angiogenesis proceeds, ECM serves essential functions in supporting key signaling events involved in regulating EC migration, invasion, proliferation, and survival. Moreover, the provisional ECM serves as a pliable scaffold wherein mechanical guidance forces are established among distal ECs, thereby providing organizational cues in the absence of cell-cell contact. Finally, through specific integrin-dependent signal transduction pathways, ECM controls the EC cytoskeleton to orchestrate the complex process of vascular morphogenesis by which proliferating ECs organize into multicellular tubes with functional lumens. Thus, the composition of ECM and therefore the regulation of ECM degradation and remodeling serves pivotally in the control of lumen and tube formation and, finally, neovessel stability and maturation.
引用
收藏
页码:1093 / 1107
页数:15
相关论文
共 192 条
[1]   ANALYSIS OF FIBRONECTIN RECEPTOR FUNCTION WITH MONOCLONAL-ANTIBODIES - ROLES IN CELL-ADHESION, MIGRATION, MATRIX ASSEMBLY, AND CYTOSKELETAL ORGANIZATION [J].
AKIYAMA, SK ;
YAMADA, SS ;
CHEN, WT ;
YAMADA, KM .
JOURNAL OF CELL BIOLOGY, 1989, 109 (02) :863-875
[2]   Colocalization of the collagen-binding proteoglycans decorin, biglycan, fibromodulin and lumican with different cells in human gingiva [J].
Alimohamad, H ;
Habijanac, T ;
Larjava, H ;
Häkkinen, L .
JOURNAL OF PERIODONTAL RESEARCH, 2005, 40 (01) :73-86
[3]   EXTRACELLULAR-MATRIX PROTEINS OF HUMAN EPIDERMAL-KERATINOCYTES AND FEEDER 3T3-CELLS [J].
ALITALO, K ;
KUISMANEN, E ;
MYLLYLA, R ;
KIISTALA, U ;
ASKOSELJAVAARA, S ;
VAHERI, A .
JOURNAL OF CELL BIOLOGY, 1982, 94 (03) :497-505
[4]   Pericytes: Cell biology and pathology [J].
Allt, G ;
Lawrenson, JG .
CELLS TISSUES ORGANS, 2001, 169 (01) :1-11
[5]  
ALOISI M, 1971, VIRCHOWS ARCH B, V8, P328
[6]   Matrix attachment regulates Fas-induced apoptosis in endothelial cells: A role for c-Flip and implications for anoikis [J].
Aoudjit, F ;
Vuori, K .
JOURNAL OF CELL BIOLOGY, 2001, 152 (03) :633-643
[7]   Anchorage-dependent regulation of the mitogen-activated protein kinase cascade by growth factors is supported by a variety of integrin α chains [J].
Aplin, AE ;
Short, SM ;
Juliano, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (44) :31223-31228
[8]   Heart valve development - Endothelial cell signaling and differentiation [J].
Armstrong, EJ ;
Bischoff, J .
CIRCULATION RESEARCH, 2004, 95 (05) :459-470
[9]   Thrombospondins 1 and 2 function as inhibitors of angiogenesis [J].
Armstrong, LC ;
Bornstein, P .
MATRIX BIOLOGY, 2003, 22 (01) :63-71
[10]   Coordinate signaling by integrins and receptor tyrosine kinases in the regulation of G1 phase cell-cycle progression [J].
Assoian, RK ;
Schwartz, MA .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2001, 11 (01) :48-53