Endothelial Ca2+ oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo

Author:

Yokota Yasuhiro1,Nakajima Hiroyuki1,Wakayama Yuki1,Muto Akira23,Kawakami Koichi23,Fukuhara Shigetomo1,Mochizuki Naoki14

Affiliation:

1. Department of Cell Biology, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan

2. Division of Molecular and Developmental Biology, National Institute of Genetics, Mishima, Japan

3. Department of Genetics, SOKENDAI (The Graduate University for Advanced Studies), National Institute of Genetics, Mishima, Japan

4. AMED-CREST, Japan Agency for Medical Research and Development, Suita, Japan

Abstract

Sprouting angiogenesis is a well-coordinated process controlled by multiple extracellular inputs, including vascular endothelial growth factor (VEGF). However, little is known about when and how individual endothelial cell (EC) responds to angiogenic inputs in vivo. Here, we visualized endothelial Ca2+ dynamics in zebrafish and found that intracellular Ca2+ oscillations occurred in ECs exhibiting angiogenic behavior. Ca2+ oscillations depended upon VEGF receptor-2 (Vegfr2) and Vegfr3 in ECs budding from the dorsal aorta (DA) and posterior cardinal vein, respectively. Thus, visualizing Ca2+ oscillations allowed us to monitor EC responses to angiogenic cues. Vegfr-dependent Ca2+ oscillations occurred in migrating tip cells as well as stalk cells budding from the DA. We investigated how Dll4/Notch signaling regulates endothelial Ca2+ oscillations and found that it was required for the selection of single stalk cell as well as tip cell. Thus, we captured spatio-temporal Ca2+ dynamics during sprouting angiogenesis, as a result of cellular responses to angiogenic inputs.

Funder

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Takeda Science Foundation

Japan Foundation for Applied Enzymology

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference51 articles.

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3. Notch-dependent VEGFR3 upregulation allows angiogenesis without VEGF–VEGFR2 signalling;Benedito;Nature,2012

4. Tumor-secreted vascular permeability factor increases cytosolic Ca2+ and von willebrand factor release in human endothelial cells;Brock;The American Journal of Pathology,1991

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