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Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice

Neovascularization of the erectile tissue emerges as a beneficial curative approach to treat erectile dysfunction (ED). Here we for the first time report the unexpected role of vasohibin-1 (VASH1), mainly known as an anti-angiogenic factor, in restoring erectile function in diabetic mice. A diabetic...

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Autores principales: Song, Kang-Moon, Kim, Woo Jean, Choi, Min-Ji, Kwon, Ki-Dong, Limanjaya, Anita, Ghatak, Kalyan, Ock, Jiyeon, Yin, Guo Nan, Sato, Yasufumi, Hong, Soon-Sun, Ryu, Ji-Kan, Suh, Jun-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807034/
https://www.ncbi.nlm.nih.gov/pubmed/33441910
http://dx.doi.org/10.1038/s41598-020-80925-7
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author Song, Kang-Moon
Kim, Woo Jean
Choi, Min-Ji
Kwon, Ki-Dong
Limanjaya, Anita
Ghatak, Kalyan
Ock, Jiyeon
Yin, Guo Nan
Sato, Yasufumi
Hong, Soon-Sun
Ryu, Ji-Kan
Suh, Jun-Kyu
author_facet Song, Kang-Moon
Kim, Woo Jean
Choi, Min-Ji
Kwon, Ki-Dong
Limanjaya, Anita
Ghatak, Kalyan
Ock, Jiyeon
Yin, Guo Nan
Sato, Yasufumi
Hong, Soon-Sun
Ryu, Ji-Kan
Suh, Jun-Kyu
author_sort Song, Kang-Moon
collection PubMed
description Neovascularization of the erectile tissue emerges as a beneficial curative approach to treat erectile dysfunction (ED). Here we for the first time report the unexpected role of vasohibin-1 (VASH1), mainly known as an anti-angiogenic factor, in restoring erectile function in diabetic mice. A diabetic patient has lower cavernous VASH1 expression than in the potent man. VASH1 was mainly expressed in endothelial cells. There were significant decreases in cavernous endothelial cell and pericyte contents in VASH1 knockout mice compared with those in wild-type mice, which resulted in impairments in erectile function. Intracavernous injection of VASH1 protein successfully restored erectile function in the diabetic mice (~ 90% of control values). VASH1 protein reinstated endothelial cells, pericytes, and endothelial cell–cell junction proteins and induced phosphorylation of eNOS (Ser1177) in the diabetic mice. The induction of angiogenic factors, such as angiopoietin-1 and vascular endothelial growth factor, is responsible for cavernous angiogenesis and the restoration of erectile function mediated by VASH1. Altogether, these findings suggest that VASH1 is proangiogenic in diabetic penis and is a new potential target for diabetic ED.
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spelling pubmed-78070342021-01-14 Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice Song, Kang-Moon Kim, Woo Jean Choi, Min-Ji Kwon, Ki-Dong Limanjaya, Anita Ghatak, Kalyan Ock, Jiyeon Yin, Guo Nan Sato, Yasufumi Hong, Soon-Sun Ryu, Ji-Kan Suh, Jun-Kyu Sci Rep Article Neovascularization of the erectile tissue emerges as a beneficial curative approach to treat erectile dysfunction (ED). Here we for the first time report the unexpected role of vasohibin-1 (VASH1), mainly known as an anti-angiogenic factor, in restoring erectile function in diabetic mice. A diabetic patient has lower cavernous VASH1 expression than in the potent man. VASH1 was mainly expressed in endothelial cells. There were significant decreases in cavernous endothelial cell and pericyte contents in VASH1 knockout mice compared with those in wild-type mice, which resulted in impairments in erectile function. Intracavernous injection of VASH1 protein successfully restored erectile function in the diabetic mice (~ 90% of control values). VASH1 protein reinstated endothelial cells, pericytes, and endothelial cell–cell junction proteins and induced phosphorylation of eNOS (Ser1177) in the diabetic mice. The induction of angiogenic factors, such as angiopoietin-1 and vascular endothelial growth factor, is responsible for cavernous angiogenesis and the restoration of erectile function mediated by VASH1. Altogether, these findings suggest that VASH1 is proangiogenic in diabetic penis and is a new potential target for diabetic ED. Nature Publishing Group UK 2021-01-13 /pmc/articles/PMC7807034/ /pubmed/33441910 http://dx.doi.org/10.1038/s41598-020-80925-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Song, Kang-Moon
Kim, Woo Jean
Choi, Min-Ji
Kwon, Ki-Dong
Limanjaya, Anita
Ghatak, Kalyan
Ock, Jiyeon
Yin, Guo Nan
Sato, Yasufumi
Hong, Soon-Sun
Ryu, Ji-Kan
Suh, Jun-Kyu
Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
title Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
title_full Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
title_fullStr Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
title_full_unstemmed Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
title_short Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
title_sort vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807034/
https://www.ncbi.nlm.nih.gov/pubmed/33441910
http://dx.doi.org/10.1038/s41598-020-80925-7
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