Angiogenesis: A Team Effort Coordinated by Notch

被引:631
作者
Phng, L. -K. [1 ]
Gerhardt, Holger [1 ]
机构
[1] Canc Res UK, Vasc Biol Lab, London Res Inst, London WC2A 3PX, England
关键词
ENDOTHELIAL-GROWTH-FACTOR; ARTERIAL-VENOUS DIFFERENTIATION; TRANSCRIPTION FACTOR HESR1; INHIBITS TUMOR-GROWTH; ARTERIOVENOUS-MALFORMATIONS; VASCULAR MORPHOGENESIS; SIGNALING PATHWAYS; IN-VITRO; CELL; VEGF;
D O I
10.1016/j.devcel.2009.01.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The past two decades of angiogenesis research have identified a wealth of pro- and antiangiogenic signals originating from the tissue environment, which control blood vessel density and function. Understanding when and how blood vessels respond to the combination of signals they encounter to achieve a balanced cellular response is a major challenge for the field of developmental and tumor angiogenesis. This review focuses on how endothelial cell-cell communication via the Notch pathway contributes to this signal integration and is essential for functional vessel patterning.
引用
收藏
页码:196 / 208
页数:13
相关论文
共 113 条
[1]   Phenotypic heterogeneity of the endothelium I. Structure, function, and mechanisms [J].
Aird, William C. .
CIRCULATION RESEARCH, 2007, 100 (02) :158-173
[2]   Brothers and Sisters Molecular Insights Into Arterial-Venous Heterogeneity [J].
Aitsebaomo, Julius ;
Portbury, Andrea L. ;
Schisler, Jonathan C. ;
Patterson, Cam .
CIRCULATION RESEARCH, 2008, 103 (09) :929-939
[3]   Microfibril-associate glycoprotein-2 (MAGP-2) promotes angiogenic cell sprouting by blocking notch signaling in endothelial cells [J].
Albig, Allan R. ;
Becenti, Darryl J. ;
Roy, Thessa G. ;
Schiemann, William P. .
MICROVASCULAR RESEARCH, 2008, 76 (01) :7-14
[4]   Transcriptome analysis of endothelial cell gene expression induced by growth on matrigel matrices: Identification and characterization of MAGP-2 and lumican as novel regulators of angiogenesis [J].
Albig A.R. ;
Roy T.G. ;
Becenti D.J. ;
Schiemann W.P. .
Angiogenesis, 2007, 10 (3) :197-216
[5]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[6]   Cellular changes in normal blood capillaries undergoing regression after inhibition of VEGF signaling [J].
Baffert, F ;
Le, T ;
Sennino, B ;
Thurston, G ;
Kuo, CJ ;
Hu-Lowe, D ;
McDonald, DM .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2006, 290 (02) :H547-H559
[7]   Loss of Notch signalling induced by Dll4 causes arterial calibre reduction by increasing endothelial cell response to angiogenic stimuli [J].
Benedito, Rui ;
Trindade, Alexandre ;
Hirashima, Masanori ;
Henrique, Domingos ;
da Costa, Luis Lopes ;
Rossant, Janet ;
Gill, Parkash S. ;
Duarte, Antonio .
BMC DEVELOPMENTAL BIOLOGY, 2008, 8
[8]   Agent-based simulation of notch-mediated tip cell selection in angiogenic sprout initialisation [J].
Bentley, Katie ;
Gerhardt, Holger ;
Bates, Paul A. .
JOURNAL OF THEORETICAL BIOLOGY, 2008, 250 (01) :25-36
[9]   Complex cell rearrangements during intersegmental vessel sprouting and vessel fusion in the zebrafish embryo [J].
Blum, Yannick ;
Belting, Heinz-Georg ;
Ellertsdottir, Elin ;
Herwig, Lukas ;
Lueders, Florian ;
Affolter, Markus .
DEVELOPMENTAL BIOLOGY, 2008, 316 (02) :312-322
[10]   Notch signalling: a simple pathway becomes complex [J].
Bray, Sarah J. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2006, 7 (09) :678-689