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Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model
Granulosa cells (GCs) play a critical role in follicular development, which cannot be separated from the assistance of theca cells (TCs). In the present study, we used a transwell system to develop three stages of goose GCs in vitro mono-culture and co-culture models, and we analyzed the morphology,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414519/ https://www.ncbi.nlm.nih.gov/pubmed/32706022 http://dx.doi.org/10.1042/BSR20200445 |
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author | Gan, Xiang Wang, Yushi Gao, Shanyan Chen, Xi Hu, Shenqiang Wang, Jiwen Hu, Jiwei Li, Liang Han, Chunchun |
author_facet | Gan, Xiang Wang, Yushi Gao, Shanyan Chen, Xi Hu, Shenqiang Wang, Jiwen Hu, Jiwei Li, Liang Han, Chunchun |
author_sort | Gan, Xiang |
collection | PubMed |
description | Granulosa cells (GCs) play a critical role in follicular development, which cannot be separated from the assistance of theca cells (TCs). In the present study, we used a transwell system to develop three stages of goose GCs in vitro mono-culture and co-culture models, and we analyzed the morphology, activity, intracellular lipid content and the expression of core genes involved in de novo lipogenesis (DNL), steroidogenesis, proliferation and apoptosis of the GCs. In the co-culture group, the activity of all three stages of GCs showed significant (P<0.01) changes, and they had a strong (P<0.01) correlation with culture time; further, the intracellular lipid deposition of hierarchical GCs was significantly different (P<0.01) between the two methods. Moreover, after co-culture, in pre-hierarchical GCs, the expression of SREBP, CYP11 and 3βHSD was promoted (P<0.01). In hierarchical GCs, the expression of ACC, SREBP, STAR, CYP11, 3βHSD and CCND1 was promoted at 48 h, but they were inhibited (P<0.05) at 96 h. In F1 GCs, the expression of ACC, FAS, SREBP, CYP11, BCL2 and CAS3 was inhibited (P<0.01). The results indicate that goose TCs had complex and time-dependent effects on the biological function of GCs at each corresponding stage, and the effects were distinct in the different stages. In addition, DNL, steroidogenesis, proliferation and apoptosis in hierarchical and F1 GCs might have some synergistic relationships in the effects of TCs on GCs. Furthermore, we speculated that TCs might play an important role in the differentiation and maturation of GCs during follicular development. |
format | Online Article Text |
id | pubmed-7414519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74145192020-08-13 Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model Gan, Xiang Wang, Yushi Gao, Shanyan Chen, Xi Hu, Shenqiang Wang, Jiwen Hu, Jiwei Li, Liang Han, Chunchun Biosci Rep Molecular Interactions Granulosa cells (GCs) play a critical role in follicular development, which cannot be separated from the assistance of theca cells (TCs). In the present study, we used a transwell system to develop three stages of goose GCs in vitro mono-culture and co-culture models, and we analyzed the morphology, activity, intracellular lipid content and the expression of core genes involved in de novo lipogenesis (DNL), steroidogenesis, proliferation and apoptosis of the GCs. In the co-culture group, the activity of all three stages of GCs showed significant (P<0.01) changes, and they had a strong (P<0.01) correlation with culture time; further, the intracellular lipid deposition of hierarchical GCs was significantly different (P<0.01) between the two methods. Moreover, after co-culture, in pre-hierarchical GCs, the expression of SREBP, CYP11 and 3βHSD was promoted (P<0.01). In hierarchical GCs, the expression of ACC, SREBP, STAR, CYP11, 3βHSD and CCND1 was promoted at 48 h, but they were inhibited (P<0.05) at 96 h. In F1 GCs, the expression of ACC, FAS, SREBP, CYP11, BCL2 and CAS3 was inhibited (P<0.01). The results indicate that goose TCs had complex and time-dependent effects on the biological function of GCs at each corresponding stage, and the effects were distinct in the different stages. In addition, DNL, steroidogenesis, proliferation and apoptosis in hierarchical and F1 GCs might have some synergistic relationships in the effects of TCs on GCs. Furthermore, we speculated that TCs might play an important role in the differentiation and maturation of GCs during follicular development. Portland Press Ltd. 2020-08-07 /pmc/articles/PMC7414519/ /pubmed/32706022 http://dx.doi.org/10.1042/BSR20200445 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). |
spellingShingle | Molecular Interactions Gan, Xiang Wang, Yushi Gao, Shanyan Chen, Xi Hu, Shenqiang Wang, Jiwen Hu, Jiwei Li, Liang Han, Chunchun Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model |
title | Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model |
title_full | Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model |
title_fullStr | Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model |
title_full_unstemmed | Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model |
title_short | Exploration of the effects of goose TCs on GCs at different follicular stages using a co-culture model |
title_sort | exploration of the effects of goose tcs on gcs at different follicular stages using a co-culture model |
topic | Molecular Interactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414519/ https://www.ncbi.nlm.nih.gov/pubmed/32706022 http://dx.doi.org/10.1042/BSR20200445 |
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