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Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure

Premature ovarian failure (POF) is one of the principal causes of female infertility, and although its causes are complex and diverse, autoimmune deficiency may be involved. Human umbilical cord mesenchymal stem cells (UCMSCs) can be used for tissue regeneration and repair. Therefore, the present st...

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Autores principales: Wang, Zhe, Wei, Quanwei, Wang, Hao, Han, Linxiao, Dai, Hongjian, Qian, Xiaoxin, Yu, Hongliang, Yin, Manqun, Shi, Fangxiong, Qi, Nianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355366/
https://www.ncbi.nlm.nih.gov/pubmed/32714395
http://dx.doi.org/10.1155/2020/3249495
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author Wang, Zhe
Wei, Quanwei
Wang, Hao
Han, Linxiao
Dai, Hongjian
Qian, Xiaoxin
Yu, Hongliang
Yin, Manqun
Shi, Fangxiong
Qi, Nianmin
author_facet Wang, Zhe
Wei, Quanwei
Wang, Hao
Han, Linxiao
Dai, Hongjian
Qian, Xiaoxin
Yu, Hongliang
Yin, Manqun
Shi, Fangxiong
Qi, Nianmin
author_sort Wang, Zhe
collection PubMed
description Premature ovarian failure (POF) is one of the principal causes of female infertility, and although its causes are complex and diverse, autoimmune deficiency may be involved. Human umbilical cord mesenchymal stem cells (UCMSCs) can be used for tissue regeneration and repair. Therefore, the present study was designed to determine the role of UCMSCs in immune factor-induced POF in rats. In this study, different concentrations of UCMSCs were injected into induced POF rats. Ovarian functions were examined by evaluating the estrus cycle, follicular morphology, hormonal secretion, and the proliferation and apoptosis of granulosa cells. Our results showed that the estrus cycle of rats returned to normal and follicular development was significantly improved after transplantation of UCMSCs. In addition, serum concentrations of 17-estradiol (E2), progesterone (P4), and anti-Müllerian hormone (AMH) increased significantly with treatment. Transplantation of UCMSCs also reduced the apoptosis of granulosa cells and promoted the proliferation of granulosa cells. All of these improvements were dose dependent. Furthermore, the results of related gene expression showed that transplanted human UCMSCs upregulated the expression of Bcl-2, AMH, and FSHR in the ovary of POF rats and downregulated the expression of caspase-3. These results further validated the potential mechanisms of promoting the release of cell growth factors and enhancing tissue regeneration and provide a theoretical basis for the clinical application of stem cells in the treatment of premature ovarian failure.
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spelling pubmed-73553662020-07-23 Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure Wang, Zhe Wei, Quanwei Wang, Hao Han, Linxiao Dai, Hongjian Qian, Xiaoxin Yu, Hongliang Yin, Manqun Shi, Fangxiong Qi, Nianmin Stem Cells Int Research Article Premature ovarian failure (POF) is one of the principal causes of female infertility, and although its causes are complex and diverse, autoimmune deficiency may be involved. Human umbilical cord mesenchymal stem cells (UCMSCs) can be used for tissue regeneration and repair. Therefore, the present study was designed to determine the role of UCMSCs in immune factor-induced POF in rats. In this study, different concentrations of UCMSCs were injected into induced POF rats. Ovarian functions were examined by evaluating the estrus cycle, follicular morphology, hormonal secretion, and the proliferation and apoptosis of granulosa cells. Our results showed that the estrus cycle of rats returned to normal and follicular development was significantly improved after transplantation of UCMSCs. In addition, serum concentrations of 17-estradiol (E2), progesterone (P4), and anti-Müllerian hormone (AMH) increased significantly with treatment. Transplantation of UCMSCs also reduced the apoptosis of granulosa cells and promoted the proliferation of granulosa cells. All of these improvements were dose dependent. Furthermore, the results of related gene expression showed that transplanted human UCMSCs upregulated the expression of Bcl-2, AMH, and FSHR in the ovary of POF rats and downregulated the expression of caspase-3. These results further validated the potential mechanisms of promoting the release of cell growth factors and enhancing tissue regeneration and provide a theoretical basis for the clinical application of stem cells in the treatment of premature ovarian failure. Hindawi 2020-07-04 /pmc/articles/PMC7355366/ /pubmed/32714395 http://dx.doi.org/10.1155/2020/3249495 Text en Copyright © 2020 Zhe Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Zhe
Wei, Quanwei
Wang, Hao
Han, Linxiao
Dai, Hongjian
Qian, Xiaoxin
Yu, Hongliang
Yin, Manqun
Shi, Fangxiong
Qi, Nianmin
Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure
title Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure
title_full Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure
title_fullStr Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure
title_full_unstemmed Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure
title_short Mesenchymal Stem Cell Therapy Using Human Umbilical Cord in a Rat Model of Autoimmune-Induced Premature Ovarian Failure
title_sort mesenchymal stem cell therapy using human umbilical cord in a rat model of autoimmune-induced premature ovarian failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355366/
https://www.ncbi.nlm.nih.gov/pubmed/32714395
http://dx.doi.org/10.1155/2020/3249495
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