VEGF coordinates interaction of pericytes and endothelial cells during vasculogenesis and experimental angiogenesis

被引:82
作者
Hagedorn, M
Balke, M
Schmidt, A
Bloch, W
Kurz, H
Javerzat, S
Rousseau, B
Wilting, J
Bikfalvi, A
机构
[1] Univ Bordeaux 1, INSERM, EO113, F-33405 Talence, France
[2] Inst Anat Med Zellbiol & Mikroskop Anat 1, Cologne, Germany
[3] Univ Freiburg, Inst Anat & Zellbiol, Freiburg, Germany
[4] Univ Gottingen, Kinderklin, Abt Padiatrie 1, D-3400 Gottingen, Germany
关键词
vascular progenitor cells; desmin; microvasculature; chick chorioallantoic membrane assay; sambucus nigra lectin; confocal microscopy analysis;
D O I
10.1002/dvdy.20020
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Biological activities of vascular enclothelial growth factor (VEGF) have been studied extensively in endothelial cells (ECs), but few data are available regarding its effects on pericytes. In murine embryoid body cultures, VEGF-induced expression of desmin and a-smooth muscle actin (alpha-SMA) in CD-31(+) cells. The number of CD-31(+)/desmin(+) vascular chords increased with VEGF treatment time and peaked during a differentiation window between 6 and 9 days after plating. In vivo, VEGF-induced elongation and migration of desmin-positive pericytes and coverage of angiogenic capillaries, as revealed by analysis of Sambucus nigra lectin-stained vascular beds of the chick chorioallantoic membrane, VEGF also caused significant decrease of intercapillary spaces, an indicator for intussusceptive vascular growth. These VEGF-mediated effects point at a more intricate interaction between ECs and pericytes cells than previously demonstrated and suggest that pericytes may be derived from EC progenitors in vitro and not only stabilize capillaries but also participate in vascular remodeling in vivo. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:23 / 33
页数:11
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