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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4437031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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