CXCL12 Signaling Is Essential for Maturation of the Ventricular Coronary Endothelial Plexus and Establishment of Functional Coronary Circulation

被引:83
作者
Cavallero, Susana [1 ]
Shen, Hua [1 ]
Yi, Christopher [2 ]
Lien, Ching-Ling [2 ,3 ]
Kumar, S. Ram [2 ]
Sucov, Henry M. [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Broad Ctr Regenerat Med & Stem Cell Res, Los Angeles, CA 90033 USA
[2] Univ So Calif, Keck Sch Med, Dept Surg, Los Angeles, CA 90033 USA
[3] Childrens Hosp, Saban Res, Los Angeles, CA 90027 USA
关键词
CHEMOKINE RECEPTOR CXCR4; CARDIOMYOCYTE PROLIFERATION; MICE LACKING; BONE-MARROW; CELLS; EXPRESSION; ARTERIES; MIGRATION; FORM; DIFFERENTIATION;
D O I
10.1016/j.devcel.2015.03.018
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Maturation of a vascular plexus is a critical and yet incompletely understood process in organ development, and known maturation factors act universally in all vascular beds. In this study, we show that CXCL12 is an organ-specific maturation factor of particular relevance in coronary arterial vasculature. In vitro, CXCL12 does not influence nascent vessel formation, but promotes higher-order complexity of preinitiated vessels. In the heart, CXCL12 is expressed principally by the epicardium, and its receptor CXCR4 is expressed by coronary endothelial cells. CXCL12 is not a chemotactic signal for endothelial cell migration, but rather acts in a paracrine manner to influence the maturation of the coronary vascular plexus. Mutants in CXCL12 signaling show an excess of immature capillary chains and a selective failure in arterial maturation, and become leaky with the onset of coronary perfusion. Failed maturation of the coronary system explains the late-gestation lethality of these mutants.
引用
收藏
页码:469 / 477
页数:9
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