MiR-30a regulates endothelial tip cell formation and arteriolar branching

Jiang Q, Lagos-Quintana M, Liu D, Shi Y, Helker C, Herzog W, Le Noble F (2013)

Publication Type: Journal article

Publication year: 2013

Journal

Hypertension American Heart Association

Book Volume: 62

Pages Range: 592-598

Journal Issue: 3

DOI: 10.1161/HYPERTENSIONAHA.113.01767

Abstract

Microvascular rarefaction increases vascular resistance and pressure in systemic arteries and is a hallmark of fixed essential hypertension. Preventing rarefaction by activation of angiogenic processes could lower blood pressure. Endothelial tip cells in angiogenic sprouts direct branching of microvascular networks; the process is regulated by microRNAs, particularly the miR-30 family. We investigated the contribution of miR-30 family members in arteriolar branching morphogenesis via delta-like 4 (Dll4)-Notch signaling in a zebrafish model. The miR-30 family consists of 5 members (miR-30a-e). Loss-of-function experiments showed that only miR-30a reduced growth of intersegmental arterioles involving impaired tip cell function. Overexpression of miR-30a stimulated tip cell behavior resulting in augmented branching of intersegmental arterioles. In vitro and in vivo reporter assays showed that miR-30a directly targets the Notch ligand Dll4, a key inhibitor of tip cell formation. Coadministration of a Dll4 targeting morpholino in miR-30a morphants rescued the branching defects. Conversely, conditional overexpression of Notch intracellular domain restored arteriolar branching in miR-30a gain-of-function embryos. In human endothelial cells, loss of miR-30a increased DLL4 protein levels, activated Notch signaling as indicated in Notch reporter assays, and augmented Notch downstream effector, HEY2 and EFNB2 (ephrin-B2), expression. In spheroid assays, miR-30a loss- and gain-of-function affected tip cell behavior, consistent with miR-30a targeting Dll4. Our data suggest that miR-30a stimulates arteriolar branching by downregulating endothelial Dll4 expression, thereby controlling endothelial tip cell behavior. These findings could have relevance to the rarefaction process and, therefore, to hypertension. © 2013 American Heart Association, Inc.

Authors with CRIS profile

Wiebke Herzog

Involved external institutions

Max-Delbrück-Centrum für Molekulare Medizin / Max Delbrück Center for Molecular Medicine (MDC) Berlin-Buch DE Germany (DE) Westfälische Wilhelms-Universität (WWU) Münster DE Germany (DE)

How to cite

APA:

Jiang, Q., Lagos-Quintana, M., Liu, D., Shi, Y., Helker, C., Herzog, W., & Le Noble, F. (2013). MiR-30a regulates endothelial tip cell formation and arteriolar branching. Hypertension, 62(3), 592-598. https://dx.doi.org/10.1161/HYPERTENSIONAHA.113.01767

MLA:

Jiang, Qiu, et al. "MiR-30a regulates endothelial tip cell formation and arteriolar branching." Hypertension 62.3 (2013): 592-598.

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