Recovery of ovarian function by human embryonic stem cell-derived mesenchymal stem cells in cisplatin-induced premature ovarian failure in mice
Autor: | Sang Woo Lyu, Eun-Young Shin, Jin Hee Eum, Mira Park, Dong Ryul Lee, Haengseok Song, Sook Young Yoon, Jeoung Eun Lee, Jung Ah Yoon, Sookyung Jung, Woo Sik Lee |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
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Population Human Embryonic Stem Cells Chemotherapy-induced premature ovarian failure Medicine (miscellaneous) Ovarian stromal cell apoptosis Ovary Primary Ovarian Insufficiency Mesenchymal Stem Cell Transplantation Biochemistry Genetics and Molecular Biology (miscellaneous) Andrology lcsh:Biochemistry Mice medicine Human embryonic stem cell-derived MSC Animals Humans lcsh:QD415-436 education Ovulation reproductive and urinary physiology media_common education.field_of_study lcsh:R5-920 business.industry Research Mesenchymal stem cell Recovery of ovarian function Mesenchymal Stem Cells Cell Biology medicine.disease Premature ovarian failure Transplantation medicine.anatomical_structure embryonic structures Molecular Medicine Female Folliculogenesis Stem cell Cisplatin business lcsh:Medicine (General) |
Zdroj: | Stem Cell Research & Therapy, Vol 11, Iss 1, Pp 1-13 (2020) Stem Cell Research & Therapy |
ISSN: | 1757-6512 |
DOI: | 10.1186/s13287-020-01769-6 |
Popis: | Background Clinical use of mesenchymal stem cells (MSCs) requires a uniform cell population, and their harvesting is invasive and produces a limited number of cells. Human embryonic stem cell-derived MSCs (hESC-MSCs) can differentiate into three germ layers and possess immunosuppressive effects in vitro. Anticancer treatment is a well-known risk factor for premature ovarian failure (POF). In this study, we investigated the effect of hESC-MSC on recovery of ovarian function in cisplatin-induced POF in mice. Methods Female mice received intraperitoneal cisplatin for 10 days. On day 12, CHA15-derived hESC-MSCs were transplanted into the mice by tail vein injection. An injection of PBS served as the negative control. Ovaries were removed 28 days after transplantation for assessment of ovarian histology, immunostaining, and fertility testing by superovulation and in vitro fertilization. hESC-MSC transplantation into mice with cisplatin-induced damage restored body weight and ovary size. Results Mean primary and primordial follicle counts in the hESC-MSC group were significantly improved compared to the PBS group (P P Conclusions hESC-MSC restored structure and function in the cisplatin-damaged ovary. Our study provides new insights into the great clinical potential of human hESC-MSC in treating POF. |
Databáze: | OpenAIRE |
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