The CXCL12/CXCR4 Axis Plays a Critical Role in Coronary Artery Development

被引:119
作者
Ivins, Sarah [1 ]
Chappell, Joel [1 ]
Vernay, Bertrand [1 ]
Suntharalingham, Jenifer [1 ]
Martineau, Alexandrine [2 ]
Mohun, Timothy J. [2 ]
Scambler, Peter J. [1 ]
机构
[1] UCL Inst Child Hlth, Dev Biol Birth Defects, London WC1N 1EH, England
[2] MRC Natl Inst Med Res, Dev Biol Div, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
CHEMOKINE RECEPTOR CXCR4; VEGF FAMILY-MEMBERS; PROGENITOR CELLS; CHICK-EMBRYO; MICE LACKING; HEART; MIGRATION; FORM; ANGIOGENESIS; ORIGIN;
D O I
10.1016/j.devcel.2015.03.026
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The chemokine CXCL12 and its receptor CXCR4 have many functions during embryonic and postnatal life. We used murine models to investigate the role of CXCL12/CXCR4 signaling in cardiac development and found that embryonic Cxcl12-null hearts lacked intra-ventricular coronary arteries (CAs) and exhibited absent or misplaced CA stems. We traced the origin of this phenotype to defects in the early stages of CA stem formation. CA stems derive from the peritruncal plexus, an encircling capillary network that invades the wall of the developing aorta. We showed that CXCL12 is present at high levels in the outflow tract, while peritruncal endothelial cells (ECs) express CXCR4. In the absence of CXCL12, ECs were abnormally localized and impaired in their ability to anastomose with the aortic lumen. We propose that CXCL12 is required for connection of peritruncal plexus ECs to the aortic endothelium and thus plays a vital role in CA formation.
引用
收藏
页码:455 / 468
页数:14
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