Cell‐autonomous notch signaling regulates endothelial cell branching and proliferation during vascular tubulogenesis

作者：Richard C.A. Sainson, Jason N. Aoto, Martin N. Nakatsu, Matthew T. Holderfield, Erin M. Conn, Erich Koller, Christopher C.W. Hughes · 发表于：The FASEB Journal · 年份：2005 · DOI：10.1096/fj.04-3172fje · 被引用次数：228 · 研究领域：Angiogenesis and VEGF in Cancer、Developmental Biology and Gene Regulation、Congenital heart defects research

The requirement for notch signaling during vascular development is well-documented but poorly understood. Embryonic and adult endothelial cells (EC) express notch and notch ligands; however, the necessity for cell-autonomous notch signaling during angiogenesis has not been determined. During angiogenesis, EC display plasticity, whereby a subset of previously quiescent cells loses polarity and becomes migratory. To investigate the role of notch in EC, we have used a three-dimensional in vitro system that models all of the early steps of angiogenesis. We find that newly forming sprouts are composed of specialized tip cells that guide the sprout and trunk cells that proliferate and rearrange to form intercellular lumens. Furthermore, we find that notch acts cell-autonomously to suppress EC proliferation, thereby regulating tube diameter. In addition, when notch signaling is blocked, tip cells divide, and both daughter cells take on a tip cell phenotype, resulting in increased branching through vessel bifurcation. In contrast, notch signaling is not required for re-establishment of EC polarity or for lumen formation. Thus, notch is used reiteratively and cell-autonomously by EC to regulate vessel diameter, to limit branching at the tip of sprouts, and to establish a mature, quiescent phenotype.