The evaluation of retinoic acid and estrogen on mouse induced pluripotent stem cells differentiation into female germ cells

dnshnmh Srm Pub Date : 2020-06-01 DOI:10.52547/sjrm.5.1.18
J. Mahabadi, H. Nikzad, Hassan Hassani Bafrani, Z. Karami, Vajihe Taghdiri Nooshabadi
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Abstract

Authors Aims: The use of stem cells has been able to treat patients with genetic and induced abnormalities and diseases such as non-obstructive azoospermia. Today, more attention has been paid to self-induced induced pluripotent stem cells (iPSCs). The aim of this study was to investigate the role of estrogen with retinoic acid on the differentiation of mouse iPSCs towards female germ cells. Methods: In this study, mouse embryonic fibroblast cells were extracted as feeding cells and inactivated. The target groups were adjusted for estrogen with retinoic acid at intervals of days 0, 4 and 7. Expression of these genes was performed by Real Time PCR technique. Results: In this study, the expression of genes such as Stra8, Stella, Ddx4 and GDF9 was evaluated. Real-time data showed that the expression of these genes increased in estrogen group on day 4 of embryoid bodies culture, while the differences were not significant on other days. Conclusion: It is very difficult to control the differentiation of mouse induced pluripotent stem cells (miPSCs) and the role of estrogen was carefully investigated in vitro in this study. Evidence suggests that female germ cells can differentiate from miPSCs in vitro. Treatment of cells with estrogen showed a greater effect on the differentiation process on day 4.
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视黄酸和雌激素对小鼠多能干细胞向雌性生殖细胞分化的影响
作者的目的:干细胞的使用已经能够治疗遗传和诱导异常以及非梗阻性无精子症等疾病的患者。目前,自诱导多能干细胞(iPSC)受到越来越多的关注。本研究的目的是研究雌激素和维甲酸在小鼠iPSC向雌性生殖细胞分化中的作用。方法:提取小鼠胚胎成纤维细胞作为饲养细胞并灭活。每隔第0、4和7天用视黄酸对靶组进行雌激素调节。通过实时PCR技术进行这些基因的表达。结果:本研究对Stra8、Stella、Ddx4和GDF9等基因的表达进行了评价。实时数据显示,雌激素组在胚状体培养的第4天,这些基因的表达增加,而其他日子的差异不显著。结论:控制小鼠诱导多能干细胞(miPSCs)的分化非常困难,本研究在体外仔细研究了雌激素的作用。有证据表明,女性生殖细胞可以在体外与miPSC分化。用雌激素处理细胞在第4天显示出对分化过程的更大影响。
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