The microRNA-30 family targets DLL4 to modulate endothelial cell behavior during angiogenesis

被引:160
作者
Bridge, Gemma [1 ]
Monteiro, Rui [2 ]
Henderson, Stephen [1 ]
Emuss, Victoria [1 ]
Lagos, Dimitris [3 ,4 ]
Georgopoulou, Dimitra [1 ]
Patient, Roger [2 ]
Boshoff, Chris [1 ]
机构
[1] UCL, UCL Canc Inst, Canc Res UK Viral Oncol Grp, London WC1E 6BT, England
[2] Univ Oxford, Weatherall Inst Mol Med, MRC, Mol Haematol Unit, Oxford, England
[3] Univ York, Dept Biol, Ctr Immunol & Infect, York YO10 5DD, N Yorkshire, England
[4] Univ York, Hull York Med Sch, York YO10 5DD, N Yorkshire, England
关键词
INHIBITS TUMOR-GROWTH; VASCULAR DEVELOPMENT; KAPOSIS-SARCOMA; UP-REGULATION; DOWN-REGULATION; IN-VIVO; ZEBRAFISH; MIR-30; NOTCH; EXPRESSION;
D O I
10.1182/blood-2012-04-423004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Delta-like 4 (DLL4), a membrane-bound ligand belonging to the Notch signaling family, plays a fundamental role in vascular development and angiogenesis. We identified a conserved microRNA family, miR-30, which targets DLL4. Overexpression of miR-30b in endothelial cells led to increased vessel number and length in an in vitro model of sprouting angiogenesis. Microinjection of miR-30 mimics into zebrafish embryos resulted in suppression of dll4 and subsequent excessive sprouting of intersegmental vessels and reduction in dorsal aorta diameter. Use of a target protector against the miR-30 site within the dll4 3'UTR up-regulated dll4 and synergized with Vegfa signaling knockdown to inhibit angiogenesis. Furthermore, restoration of miR-30b or miR-30c expression during Kaposi sarcoma herpesvirus (KSHV) infection attenuated viral induction of DLL4. Together these results demonstrate that the highly conserved molecular targeting of DLL4 by the miR-30 family regulates angiogenesis. (Blood. 2012; 120(25): 5063-5072)
引用
收藏
页码:5063 / 5072
页数:10
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