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Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents

The bio-engineered ovary is an essential technology for treating female infertility. Especially the development of relevant in vitro models could be a critical step in a drug study. Herein, we develop a semi-opened culturing system (SOCS) strategy that maintains a 3D structure of follicles during th...

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Autores principales: Ye, Min, Shan, Yiran, Lu, Bingchuan, Luo, Hao, Li, Binhan, Zhang, Yanmei, Wang, Zixuan, Guo, Yuzhi, Ouyang, Liliang, Gu, Jin, Xiong, Zhuo, Zhang, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017366/
https://www.ncbi.nlm.nih.gov/pubmed/36936809
http://dx.doi.org/10.1016/j.bioactmat.2023.02.029
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author Ye, Min
Shan, Yiran
Lu, Bingchuan
Luo, Hao
Li, Binhan
Zhang, Yanmei
Wang, Zixuan
Guo, Yuzhi
Ouyang, Liliang
Gu, Jin
Xiong, Zhuo
Zhang, Ting
author_facet Ye, Min
Shan, Yiran
Lu, Bingchuan
Luo, Hao
Li, Binhan
Zhang, Yanmei
Wang, Zixuan
Guo, Yuzhi
Ouyang, Liliang
Gu, Jin
Xiong, Zhuo
Zhang, Ting
author_sort Ye, Min
collection PubMed
description The bio-engineered ovary is an essential technology for treating female infertility. Especially the development of relevant in vitro models could be a critical step in a drug study. Herein, we develop a semi-opened culturing system (SOCS) strategy that maintains a 3D structure of follicles during the culture. Based on the SOCS, we further developed micro-cavity ovary (MCO) with mouse follicles by the microsphere-templated technique, where sacrificial gelatin microspheres were mixed with photo-crosslinkable gelatin methacryloyl (GelMA) to engineer a micro-cavity niche for follicle growth. The semi-opened MCO could support the follicle growing to the antral stage, secreting hormones, and ovulating cumulus-oocyte complex out of the MCO without extra manipulation. The MCO-ovulated oocyte exhibits a highly similar transcriptome to the in vivo counterpart (correlation of 0.97) and can be fertilized. Moreover, we found that a high ROS level could affect the cumulus expansion, which may result in anovulation disorder. The damage could be rescued by melatonin, but the end of cumulus expansion was 3h earlier than anticipation, validating that MCO has the potential for investigating ovarian toxic agents in vitro. We provide a novel approach for building an in vitro ovarian model to recapitulate ovarian functions and test chemical toxicity, suggesting it has the potential for clinical research in the future.
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spelling pubmed-100173662023-03-17 Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents Ye, Min Shan, Yiran Lu, Bingchuan Luo, Hao Li, Binhan Zhang, Yanmei Wang, Zixuan Guo, Yuzhi Ouyang, Liliang Gu, Jin Xiong, Zhuo Zhang, Ting Bioact Mater Article The bio-engineered ovary is an essential technology for treating female infertility. Especially the development of relevant in vitro models could be a critical step in a drug study. Herein, we develop a semi-opened culturing system (SOCS) strategy that maintains a 3D structure of follicles during the culture. Based on the SOCS, we further developed micro-cavity ovary (MCO) with mouse follicles by the microsphere-templated technique, where sacrificial gelatin microspheres were mixed with photo-crosslinkable gelatin methacryloyl (GelMA) to engineer a micro-cavity niche for follicle growth. The semi-opened MCO could support the follicle growing to the antral stage, secreting hormones, and ovulating cumulus-oocyte complex out of the MCO without extra manipulation. The MCO-ovulated oocyte exhibits a highly similar transcriptome to the in vivo counterpart (correlation of 0.97) and can be fertilized. Moreover, we found that a high ROS level could affect the cumulus expansion, which may result in anovulation disorder. The damage could be rescued by melatonin, but the end of cumulus expansion was 3h earlier than anticipation, validating that MCO has the potential for investigating ovarian toxic agents in vitro. We provide a novel approach for building an in vitro ovarian model to recapitulate ovarian functions and test chemical toxicity, suggesting it has the potential for clinical research in the future. KeAi Publishing 2023-03-07 /pmc/articles/PMC10017366/ /pubmed/36936809 http://dx.doi.org/10.1016/j.bioactmat.2023.02.029 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ye, Min
Shan, Yiran
Lu, Bingchuan
Luo, Hao
Li, Binhan
Zhang, Yanmei
Wang, Zixuan
Guo, Yuzhi
Ouyang, Liliang
Gu, Jin
Xiong, Zhuo
Zhang, Ting
Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents
title Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents
title_full Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents
title_fullStr Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents
title_full_unstemmed Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents
title_short Creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents
title_sort creating a semi-opened micro-cavity ovary through sacrificial microspheres as an in vitro model for discovering the potential effect of ovarian toxic agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017366/
https://www.ncbi.nlm.nih.gov/pubmed/36936809
http://dx.doi.org/10.1016/j.bioactmat.2023.02.029
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