Revealing the role of phospholipase Cβ3 in the regulation of VEGF-induced vascular permeability

Author:

Hoeppner Luke H.1,Phoenix Kathryn N.2,Clark Karl J.1,Bhattacharya Resham1,Gong Xun1,Sciuto Tracey E.34,Vohra Pawan1,Suresh Sandip1,Bhattacharya Santanu1,Dvorak Ann M.34,Ekker Stephen C.1,Dvorak Harold F.34,Claffey Kevin P.2,Mukhopadhyay Debabrata1

Affiliation:

1. Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, MN;

2. Department of Cell Biology, University of Connecticut Health Center, Farmington, CT; and

3. Center for Vascular Biology Research and

4. Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA

Abstract

AbstractVEGF induces vascular permeability (VP) in ischemic diseases and cancer, leading to many pathophysiological consequences. The molecular mechanisms by which VEGF acts to induce hyperpermeability are poorly understood and in vivo models that easily facilitate real-time, genetic studies of VP do not exist. In the present study, we report a heat-inducible VEGF transgenic zebrafish (Danio rerio) model through which VP can be monitored in real time. Using this approach with morpholino-mediated gene knock-down and knockout mice, we describe a novel role of phospholipase Cβ3 as a negative regulator of VEGF-mediated VP by regulating intracellular Ca2+ release. Our results suggest an important effect of PLCβ3 on VP and provide a new model with which to identify genetic regulators of VP crucial to several disease processes.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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