Dicer-dependent endothelial microRNAs are necessary for postnatal angiogenesis

被引:392
作者
Suarez, Yajaira [2 ]
Fernandez-Hernando, Carlos [1 ]
Yu, Jun [1 ]
Gerber, Scott A. [2 ]
Harrison, Kenneth D. [1 ]
Pober, Jordan S. [2 ]
Iruela-Arispe, M. Luisa [3 ]
Merkenschlager, Matthias [4 ]
Sessa, William C. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pharmacol, Vasc Biol & Therapeut Program, New Haven, CT 06519 USA
[2] Yale Univ, Sch Med, Dept Immunobiol, Vasc Biol & Therapeut Program, New Haven, CT 06519 USA
[3] Univ Calif Los Angeles, Dept Mol Cellular & Dev Biol, Los Angeles, CA 90095 USA
[4] Univ London Imperial Coll Sci Technol & Med, Med Res Council Clin Sci Ctr, Lymphocyte Dev Grp, London W12 0NN, England
基金
英国医学研究理事会;
关键词
endothelium; VEGF;
D O I
10.1073/pnas.0804597105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Posttranscriptional gene regulation by microRNAs (miRNAs) is important for many aspects of development, homeostasis, and disease. Here, we show that reduction of endothelial miRNAs by cell-specific inactivation of Dicer, the terminal endonuclease responsible for the generation of miRNAs, reduces postnatal angiogenic response to a variety of stimuli, including exogenous VEGF, tumors, limb ischemia, and wound healing. Furthermore, VEGF regulated the expression of several miRNAs including the up-regulation of components of the c-Myc oncogenic cluster miR-17-92. Transfection of endothelial cells with components of the miR-17-92 cluster, induced by VEGF treatment, rescued the induced expression of thrombospondin-1 and the defect in endothelial cell proliferation and morphogenesis initiated by the loss of Dicer. Thus, endothelial miRNAs regulate postnatal angiogenesis and VEGF induces the expression of miRNAs implicated in the regulation of an integrated angiogenic response.
引用
收藏
页码:14082 / 14087
页数:6
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