Arteriolar and venular patterning in retinas of mice selectively expressing VEGF isoforms

被引:382
作者
Stalmans, I
Ng, YS
Rohan, R
Fruttiger, M
Bouché, A
Yuce, A
Fujisawa, H
Hermans, B
Shani, M
Jansen, S
Hicklin, D
Anderson, DJ
Gardiner, T
Hammes, HP
Moons, L
Dewerchin, M
Collen, D
Carmeliet, P
D'Amore, PA
机构
[1] Katholieke Univ Leuven VIB, Ctr Transgene Technol & Gene Therapy, B-3000 Leuven, Belgium
[2] Harvard Univ, Sch Med, Schepens Eye Res Inst, Dept Pathol & Ophthalmol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Childrens Hosp, Boston, MA 02115 USA
[4] UCL, Wolfson Inst Biomed Res, London, England
[5] Univ Giessen, Dept Internal Med 3, Giessen, Germany
[6] Nagoya Univ, Dept Mol Biol, Nagoya, Aichi, Japan
[7] Agr Res Org, Volcani Ctr, Inst Anim Sci, IL-50250 Bet Dagan, Israel
[8] ImClone Syst Inc, Dept Immunol, New York, NY USA
[9] CALTECH, Div Biol, Pasadena, CA 91125 USA
[10] CALTECH, Howard Hughes Med Inst, Pasadena, CA 91125 USA
[11] Queens Univ Belfast, Inst Clin Sci, Belfast, Antrim, North Ireland
[12] Univ Clin, Dept Med, Mannheim, Germany
关键词
D O I
10.1172/jci0214362
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The murine VEGF gene is alternatively transcribed to yield the VEGF(120), VEGF(164), and VEGF(188) isoforms, which differ in their potential to bind to heparan sulfate and neuropilin-1 and to stimulate endothelial growth. Here, their role in retinal vascular development was studied in mice selectively expressing single isoforms. VEGF(164/164) mice were normal, healthy, and had normal retinal angiogenesis. In contrast, VEGF(120/120) Mice exhibited severe defects in vascular outgrowth and patterning, whereas VEGF(188/188) mice displayed normal venular outgrowth but impaired arterial development. It is noteworthy that neuropilin-1, a receptor for VEGF164, was predominantly expressed in retinal arterioles. These findings reveal distinct roles of the various VEGF isoforms in vascular patterning and arterial development in the retina.
引用
收藏
页码:327 / 336
页数:10
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