Abstract
Premature ovarian failure (POF) is a refractory disease; one of the most important goals of treatment is to improve fertility. In the study, collagen scaffold loaded with human umbilical cord–derived mesenchymal stem cells (collagen/UC-MSCs) transplantation in POF mice preserved ovarian function, as supported by increased estrogen (E2) and anti-Mullerian hormone (AMH) levels, increased ovarian volume, and an increased number of antral follicles. Immunohistochemistry results of Ki67 indicated transplantation of collagen/UC-MSCs promoted granulosa cell proliferation, which is crucial to oocyte maturation and follicular development. Additionally, transplantation of collagen/UC-MSCs significantly promoted ovarian angiogenesis with the increased expression of CD31. In general, collagen/UC-MSCs transplantation probably is an effective therapeutic strategy of POF.
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Funding
Haixiang Sun is supported by National Nature Science Foundation of China (31571189), Strategic Priority Research Program of the Chinese Academy of Sciences (XDA01030501), Jiangsu Province Social Development Project (BE2018602). This work is also supported from Lijun Ding by grants National Key Research and Development Program of China (2018YFC1004700), National Nature Science Foundation of China (81871128, 81571391, 30900847), Nanjing Medical Science Development Project (JQX14004, ZKX16042), and Jiangsu Provincial Medical Youth Talent (QNRC2016006). Shanshan Wang is supported by National Nature Science Foundation of China (81601277).
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Editor: Tetsuji Okamoto
Yanjun Yang, Lei Lei, and Shanshan Wang are equal contributors
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Supplementary Fig. 1
The body weight of POF mice after collagen/UC-MSCs transplantation. (a) The body weight of mice underwent different treatments. (PNG 29 kb)
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Yang, Y., Lei, L., Wang, S. et al. Transplantation of umbilical cord–derived mesenchymal stem cells on a collagen scaffold improves ovarian function in a premature ovarian failure model of mice. In Vitro Cell.Dev.Biol.-Animal 55, 302–311 (2019). https://doi.org/10.1007/s11626-019-00337-4
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DOI: https://doi.org/10.1007/s11626-019-00337-4