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


Autoria(s): Bellomo, D.; Headrick, J. P.; Silins, G. U.; Paterson, C. A.; Thomas, P. S.; Gartside, M.; Mould, A.; Cahill, M. M.; Tonks, I. D.; Grimmond, S. M.; Wells, C. A.; Little, M. H.; Cummings, M. C.; Hayward, N. K.; Kay, G. F.
Data(s)

04/02/2000

Resumo

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.

Identificador

http://espace.library.uq.edu.au/view/UQ:84711

Idioma(s)

eng

Publicador

Lippincott, Williams & Wilkins

Palavras-Chave #Cardiac & Cardiovascular Systems #Hematology #Peripheral Vascular Disease #Angiogenesis #Cardiac Ischemia #Coronary Vasculature #Tyrosine Kinase #Expression #Mouse #Circulation #Cells #Organization #Lethality #Responses #Rat #321020 Pathology #730106 Cardiovascular system and diseases #C1
Tipo

Journal Article