Apelin, the ligand for the endothelial G-protein-coupled receptor, APJ, is a potent angiogenic factor required for normal vascular development of the frog embryo

被引:261
作者
Cox, Christopher M.
D'Agostino, Susan L.
Miller, Melanie K.
Heimark, Ronald L.
Krieg, Paul A.
机构
[1] Univ Arizona, Hlth Sci Ctr, Dept Cell Biol & Anat, Tucson, AZ 85724 USA
[2] Univ Arizona, Hlth Sci Ctr, Dept Surg, Tucson, AZ 85724 USA
关键词
angiogenesis; apelin; APJ; Xenopus; CAM assay; hypoxia; endothelial mitogen;
D O I
10.1016/j.ydbio.2006.04.452
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The peptide growth factor apelin is the high affinity ligand for the G-protein-coupled receptor APJ. During embryonic development of mouse and frog, APJ receptor is expressed at high levels in endothelial precursor cells and in nascent vascular structures. Characterization of Xenopus apelin shows that the sequence of the bioactive region of the peptide is perfectly conserved between frogs and mammals. Embryonic expression studies indicate that apelin is expressed in, or immediately adjacent to, a subset of the developing vascular structures, particularly the intersegmental vessels. Experimental inhibition of either apelin or AN expression, using antisense morpholino oligos, results in elimination or disruption of intersegmental vessels in a majority of embryos. In gain of function experiments, apelin peptide is a potent angiogenic factor when tested using two in vivo angiogenesis assays, the frog embryo and the chicken chorioallantoic membrane. Furthermore, studies using the mouse brain microvascular cell line bEnd.3 show that apelin acts as a mitogenic, chemotactic and anti-apoptotic agent for endothelial cells in culture. Finally, we show that, similar to a number of other angiogenic factors, expression of the apelin gene is increased under conditions of hypoxia. Taken together, these studies indicate that apelin is required for normal vascular development in the frog embryo and has properties consistent with a role during normal and pathological angiogenesis. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:177 / 189
页数:13
相关论文
共 71 条
[1]  
Ahmad SA, 2001, CANCER RES, V61, P1255
[2]  
Baltzinger M, 1999, DEV DYNAM, V216, P420, DOI 10.1002/(SICI)1097-0177(199912)216:4/5<420::AID-DVDY10>3.0.CO
[3]  
2-C
[4]   Dual control of glut1 glucose transporter gene expression by hypoxia and by inhibition of oxidative phosphorylation [J].
Behrooz, A ;
IsmailBeigi, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (09) :5555-5562
[5]   Apelin has in vivo inotropic effects on normal and failing hearts [J].
Berry, MF ;
Pirolli, TJ ;
Jayasankar, V ;
Burdick, J ;
Morine, KJ ;
Gardner, TJ ;
Woo, YJ .
CIRCULATION, 2004, 110 (11) :II187-II193
[6]   Vascular actions of calcitonin gene-related peptide and adrenomedullin [J].
Brain, SD ;
Grant, AD .
PHYSIOLOGICAL REVIEWS, 2004, 84 (03) :903-934
[7]   REQUIREMENT OF VASCULAR INTEGRIN ALPHA(V)BETA(3) FOR ANGIOGENESIS [J].
BROOKS, PC ;
CLARK, RAF ;
CHERESH, DA .
SCIENCE, 1994, 264 (5158) :569-571
[8]   Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele [J].
Carmeliet, P ;
Ferreira, V ;
Breier, G ;
Pollefeyt, S ;
Kieckens, L ;
Gertsenstein, M ;
Fahrig, M ;
Vandenhoeck, A ;
Harpal, K ;
Eberhardt, C ;
Declercq, C ;
Pawling, J ;
Moons, L ;
Collen, D ;
Risau, W ;
Nagy, A .
NATURE, 1996, 380 (6573) :435-439
[9]   Novel role for the potent endogenous inotrope apelin in human cardiac dysfunction [J].
Chen, MM ;
Ashley, EA ;
Deng, DXF ;
Tsalenko, A ;
Deng, A ;
Tabibiazar, R ;
Ben-Dor, A ;
Fenster, B ;
Yang, E ;
King, JY ;
Fowler, M ;
Robbins, R ;
Johnson, FL ;
Bruhn, L ;
McDonagh, T ;
Dargie, H ;
Yakhini, Z ;
Tsao, PS ;
Quertermous, T .
CIRCULATION, 2003, 108 (12) :1432-1439
[10]   Venous dilator effect of apelin, an endogenous peptide ligand for the orphan APJ receptor, in conscious rats [J].
Cheng, X ;
Cheng, XS ;
Pang, CCY .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 470 (03) :171-175