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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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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 |
format | Online Article Text |
id | pubmed-4720519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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