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Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo

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 C...

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Autores principales: Yokota, Yasuhiro, Nakajima, Hiroyuki, Wakayama, Yuki, Muto, Akira, Kawakami, Koichi, Fukuhara, Shigetomo, Mochizuki, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720519/
https://www.ncbi.nlm.nih.gov/pubmed/26588168
http://dx.doi.org/10.7554/eLife.08817
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author Yokota, Yasuhiro
Nakajima, Hiroyuki
Wakayama, Yuki
Muto, Akira
Kawakami, Koichi
Fukuhara, Shigetomo
Mochizuki, Naoki
author_facet Yokota, Yasuhiro
Nakajima, Hiroyuki
Wakayama, Yuki
Muto, Akira
Kawakami, Koichi
Fukuhara, Shigetomo
Mochizuki, Naoki
author_sort Yokota, Yasuhiro
collection PubMed
description 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 Ca(2+) dynamics in zebrafish and found that intracellular Ca(2+) oscillations occurred in ECs exhibiting angiogenic behavior. Ca(2+) oscillations depended upon VEGF receptor-2 (Vegfr2) and Vegfr3 in ECs budding from the dorsal aorta (DA) and posterior cardinal vein, respectively. Thus, visualizing Ca(2+) oscillations allowed us to monitor EC responses to angiogenic cues. Vegfr-dependent Ca(2+) oscillations occurred in migrating tip cells as well as stalk cells budding from the DA. We investigated how Dll4/Notch signaling regulates endothelial Ca(2+) oscillations and found that it was required for the selection of single stalk cell as well as tip cell. Thus, we captured spatio-temporal Ca(2+) dynamics during sprouting angiogenesis, as a result of cellular responses to angiogenic inputs. DOI: http://dx.doi.org/10.7554/eLife.08817.001
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spelling pubmed-47205192016-03-17 Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo Yokota, Yasuhiro Nakajima, Hiroyuki Wakayama, Yuki Muto, Akira Kawakami, Koichi Fukuhara, Shigetomo Mochizuki, Naoki eLife Developmental Biology and Stem Cells 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 Ca(2+) dynamics in zebrafish and found that intracellular Ca(2+) oscillations occurred in ECs exhibiting angiogenic behavior. Ca(2+) oscillations depended upon VEGF receptor-2 (Vegfr2) and Vegfr3 in ECs budding from the dorsal aorta (DA) and posterior cardinal vein, respectively. Thus, visualizing Ca(2+) oscillations allowed us to monitor EC responses to angiogenic cues. Vegfr-dependent Ca(2+) oscillations occurred in migrating tip cells as well as stalk cells budding from the DA. We investigated how Dll4/Notch signaling regulates endothelial Ca(2+) oscillations and found that it was required for the selection of single stalk cell as well as tip cell. Thus, we captured spatio-temporal Ca(2+) dynamics during sprouting angiogenesis, as a result of cellular responses to angiogenic inputs. DOI: http://dx.doi.org/10.7554/eLife.08817.001 eLife Sciences Publications, Ltd 2015-11-20 /pmc/articles/PMC4720519/ /pubmed/26588168 http://dx.doi.org/10.7554/eLife.08817 Text en © 2015, Yokota et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology and Stem Cells
Yokota, Yasuhiro
Nakajima, Hiroyuki
Wakayama, Yuki
Muto, Akira
Kawakami, Koichi
Fukuhara, Shigetomo
Mochizuki, Naoki
Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo
title Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo
title_full Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo
title_fullStr Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo
title_full_unstemmed Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo
title_short Endothelial Ca(2+) oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo
title_sort endothelial ca(2+) oscillations reflect vegfr signaling-regulated angiogenic capacity in vivo
topic Developmental Biology and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720519/
https://www.ncbi.nlm.nih.gov/pubmed/26588168
http://dx.doi.org/10.7554/eLife.08817
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