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

Author:

Bridge Gemma1,Monteiro Rui2,Henderson Stephen1,Emuss Victoria1,Lagos Dimitris3,Georgopoulou Dimitra1,Patient Roger2,Boshoff Chris1

Affiliation:

1. Cancer Research UK Viral Oncology Group, UCL Cancer Institute, University College London, London, United Kingdom;

2. MRC Molecular Haematology Unit, The Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom; and

3. Centre for Immunology and Infection, Department of Biology and Hull York Medical School, University of York, York, United Kingdom

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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