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Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice

Secreted Slit proteins and their Roundabout (Robo) receptors act as a repulsive cue to preventaxons from migrating to inappropriate locations during the development of the nervous system. Slit/Robo has also been implicated in reproductive system development, but the molecular mechanism of the Slit/R...

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Autores principales: Li, Jiangchao, Ye, Yuxiang, Zhang, Renli, Zhang, Lili, Hu, Xiwen, Han, Dong, Chen, Jiayuan, He, Xiaodong, Wang, Guang, Yang, Xuesong, Wang, Lijing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437031/
https://www.ncbi.nlm.nih.gov/pubmed/25988316
http://dx.doi.org/10.1038/srep09720
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author Li, Jiangchao
Ye, Yuxiang
Zhang, Renli
Zhang, Lili
Hu, Xiwen
Han, Dong
Chen, Jiayuan
He, Xiaodong
Wang, Guang
Yang, Xuesong
Wang, Lijing
author_facet Li, Jiangchao
Ye, Yuxiang
Zhang, Renli
Zhang, Lili
Hu, Xiwen
Han, Dong
Chen, Jiayuan
He, Xiaodong
Wang, Guang
Yang, Xuesong
Wang, Lijing
author_sort Li, Jiangchao
collection PubMed
description Secreted Slit proteins and their Roundabout (Robo) receptors act as a repulsive cue to preventaxons from migrating to inappropriate locations during the development of the nervous system. Slit/Robo has also been implicated in reproductive system development, but the molecular mechanism of the Slit/Robo pathway in the reproductive system remains poorly understood. Using a transgenic mouse model, we investigated the function of the Slit/Robo pathway on ovarian follicle development and atresia. We first demonstrated that more offspring were born to mice with a partial knockout of the Robo1/2 genes in mice. We next showed that Robo1 and Robo2 are strongly expressed in ovarian granulosacells. Apoptosis in granulosa cells was reduced when Robo1/2 were partially knocked out, and this observation was further verified by in vitro Robo1/2 knockout experiments in mouse and human granulosa cells. We also found that ovarian angiogenesis wasenhanced by a partial lack of Robo1/2 genes. In summary, our data suggest that the Slit/Robo pathway can impact follicle development and atresia by influencinggranulosa cell apoptosis.
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spelling pubmed-44370312015-06-01 Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice Li, Jiangchao Ye, Yuxiang Zhang, Renli Zhang, Lili Hu, Xiwen Han, Dong Chen, Jiayuan He, Xiaodong Wang, Guang Yang, Xuesong Wang, Lijing Sci Rep Article Secreted Slit proteins and their Roundabout (Robo) receptors act as a repulsive cue to preventaxons from migrating to inappropriate locations during the development of the nervous system. Slit/Robo has also been implicated in reproductive system development, but the molecular mechanism of the Slit/Robo pathway in the reproductive system remains poorly understood. Using a transgenic mouse model, we investigated the function of the Slit/Robo pathway on ovarian follicle development and atresia. We first demonstrated that more offspring were born to mice with a partial knockout of the Robo1/2 genes in mice. We next showed that Robo1 and Robo2 are strongly expressed in ovarian granulosacells. Apoptosis in granulosa cells was reduced when Robo1/2 were partially knocked out, and this observation was further verified by in vitro Robo1/2 knockout experiments in mouse and human granulosa cells. We also found that ovarian angiogenesis wasenhanced by a partial lack of Robo1/2 genes. In summary, our data suggest that the Slit/Robo pathway can impact follicle development and atresia by influencinggranulosa cell apoptosis. Nature Publishing Group 2015-05-19 /pmc/articles/PMC4437031/ /pubmed/25988316 http://dx.doi.org/10.1038/srep09720 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Li, Jiangchao
Ye, Yuxiang
Zhang, Renli
Zhang, Lili
Hu, Xiwen
Han, Dong
Chen, Jiayuan
He, Xiaodong
Wang, Guang
Yang, Xuesong
Wang, Lijing
Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
title Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
title_full Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
title_fullStr Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
title_full_unstemmed Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
title_short Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
title_sort robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437031/
https://www.ncbi.nlm.nih.gov/pubmed/25988316
http://dx.doi.org/10.1038/srep09720
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