Mice lacking the vascular endothelial growth factor-B gene (Vegfb) have smaller hearts, dysfunctional coronary vasculature, and impaired recovery from cardiac ischemia

被引:226
作者
Bellomo, D
Headrick, JP
Silins, GU
Paterson, CA
Thomas, PS
Gartside, M
Mould, A
Cahill, MM
Tonks, ID
Grimmond, SM
Townson, S
Wells, C
Little, M
Cummings, MC
Hayward, NK
Kay, GF
机构
[1] Univ Queensland, Queensland Inst Med Res, Joint Expt Oncol Program, QCF Transgen Lab & Human Genet Lab, Brisbane, Qld, Australia
[2] Univ Queensland, Dept Pathol, Brisbane, Qld, Australia
[3] Griffith Univ, Southport, Qld, Australia
[4] Natl Heart & Lung Inst, Dept Cardiothorac Surg, Imperial Coll, Sch Med, London SW3 6LY, England
[5] Univ Queensland, Ctr Cellular & Mol Biol, Brisbane, Qld, Australia
关键词
angiogenesis; cardiac ischemia; coronary vasculature;
D O I
10.1161/01.RES.86.2.e29
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular endothelial growth factor-B (VEGF-B) is closely related to VEGF-A, an effector of blood vessel growth during development and disease and a strong candidate for angiogenic therapies. To further study the in vivo function of VEGF-B, we have generated Vegfb knockout mice (Vegfb(-/-)). Unlike Vegfa knockout mice, which die during embryogenesis, Vegfb(-/-) mice are healthy and fertile. Despite appearing overtly normal, Vegfb(-/-) hearts are reduced in size and display vascular dysfunction after coronary occlusion and impaired recovery from experimentally induced myocardial ischemia. These findings reveal a role for VEGF-B in the development or function of coronary vasculature and suggest potential clinical use in therapeutic angiogenesis. The full text of this article is available at http://www.circresaha.org.
引用
收藏
页码:E29 / E35
页数:13
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