New insights into bone morphogenetic protein signaling: focus on angiogenesis

被引:45
作者
Moreno-Miralles, Isabel
Schisler, Jonathan C.
Patterson, Cam [1 ,2 ]
机构
[1] Univ N Carolina, Div Cardiol, Carolina Cardiovasc Biol Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
关键词
angiogenesis; bone morphogenetic protein; bone morphogenetic protein endothelial cell precursor-derived regulator; cyclooxygenase; 2; endothelial cells; extracellular signal-regulated kinase; gremlin; matrix gamma-carboxyglutamate protein; micro-RNA; myosin-X; MATRIX GLA PROTEIN; ENDOTHELIAL-CELLS; TRANSCRIPTION FACTORS; BMP; CROSSVEINLESS-2; EXPRESSION; SMAD1; PATHWAYS; MOUSE; GASTRULATION;
D O I
10.1097/MOH.0b013e32832a07d6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review The role of bone morphogenetic proteins (BMPs) in vasculogenesis is still not well understood, despite many recent developments in this area of research. In this review, we discuss the most recent studies that identify new critical mechanisms through which BMP signaling acts with a focus on angiogenesis. Recent findings New evidence brought to light over the last few years suggests that BMP-binding proteins, formerly thought of as antagonists, can also increase BMP activity under certain conditions. It has also recently been determined that components of the extracellular matrix are involved in the BMP signaling pathways that regulate angiogenesis. Through the BMP pathway, myosin-X and cyclooxygenase 2 serve as target genes that have been determined to play a role in blood vessel formation. BMPs also conduct Smad-independent signaling and crosstalk with other pathways. Finally, BMPs have been shown to play an antiangiogenic role in specific settings. Summary Better understanding of the BMP signaling pathway and its regulators can have potentially great effects on therapeutic strategies from cardiovascular disease to cancer.
引用
收藏
页码:195 / 201
页数:7
相关论文
共 57 条
[21]   Essential pro-Bmp roles of crossveinless 2 in mouse organogenesis [J].
Ikeya, Makoto ;
Kawada, Masako ;
Kiyonari, Hiroshi ;
Sasai, Noriaki ;
Nakao, Kazuki ;
Furuta, Yasuhide ;
Sasai, Yoshiki .
DEVELOPMENT, 2006, 133 (22) :4463-4473
[22]  
Kane R, 2008, MOL VIS, V14, P1138
[23]   Inhibitory Smad transcription factors protect arterial endothelial cells from apoptosis induced by BMP4 [J].
Kiyono, M. ;
Shibuya, M. .
ONCOGENE, 2006, 25 (54) :7131-7137
[24]   Bone morphogenetic protein 4 mediates apoptosis of capillary endothelial cells during rat pupillary membrane regression [J].
Kiyono, M ;
Shibuya, M .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (13) :4627-4636
[25]  
Koki Alane T, 2002, Cancer Control, V9, P28
[26]   Opposing BMP and EGF signalling pathways converge on the TGF-beta family mediator Smad1 [J].
Kretzschmar, M ;
Doody, J ;
Massague, J .
NATURE, 1997, 389 (6651) :618-622
[27]  
Langenfeld EM, 2004, MOL CANCER RES, V2, P141
[28]  
Larraín J, 2001, DEVELOPMENT, V128, P4439
[29]   Targeted mutagenesis of Smad1 reveals an essential role in chorioallantoic fusion [J].
Lechleider, RJ ;
Ryan, JL ;
Garrett, L ;
Eng, C ;
Deng, CX ;
Wynshaw-Boris, A ;
Roberts, AB .
DEVELOPMENTAL BIOLOGY, 2001, 240 (01) :157-167
[30]  
Mathura JR, 2000, INVEST OPHTH VIS SCI, V41, P592