Local Guidance of Emerging Vessel Sprouts Requires Soluble Flt-1

被引:171
作者
Chappell, John C. [2 ,3 ]
Taylor, Sarah M. [2 ,3 ]
Ferrara, Napoleone [1 ]
Bautch, Victoria L. [2 ,3 ,4 ]
机构
[1] Genentech Inc, San Francisco, CA 94080 USA
[2] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Carolina Cardiovasc Biol Ctr, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
ENDOTHELIAL GROWTH-FACTOR; VASCULAR DEVELOPMENT; BRANCHING MORPHOGENESIS; VEGF; RECEPTOR; CELLS; NOTCH; DIFFERENTIATION; VASCULOGENESIS; ANGIOGENESIS;
D O I
10.1016/j.devcel.2009.07.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Blood vessel networks form via sprouting of endothelial cells from parent vessels. Extrinsic cues guide sprouts after they leave the initiation site, but these cues are likely insufficient to regulate initial outward movement, and many embryonic vessel networks form in the absence of a strong extrinsic gradient. We hypothesized that nascent sprouts are guided by spatial cues produced along their own vessels, and that soluble Flt-1 (sFlt-1) participates in this guidance. Analysis of developing vessels with perturbed flt-1 function revealed misguided emerging sprouts, and transgenic sFlt-1 rescued sprout guidance parameters. sflt-1 activity in endothelial cells immediately adjacent to the emerging sprout significantly improved local sprout guidance. Thus, we propose that a vessel-intrinsic system initially guides emerging sprouts away from the parent vessel, utilizing spatially regulated expression of sFlt-1 in conjunction with exogenous VEGF-A. Local sprout guidance defects are predicted to contribute to vessel dysmorphogenesis during perturbed development and disease.
引用
收藏
页码:377 / 386
页数:10
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