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转录组分析在高温抑制精原干细胞体外分化中的作用。

Transcriptome Analysis in High Temperature Inhibiting Spermatogonial Stem Cell Differentiation In Vitro.

机构信息

Key Laboratory of Fertility Preservation and Maintenance of Ministry of Education, and Key Laboratory of Reproduction and Genetics of Ningxia Hui Autonomous Region, Department of Human Anatomy and Histoembryology, School of Basic Medical Science, Ningxia Medical University, Yinchuan, 750004, China.

出版信息

Reprod Sci. 2023 Jun;30(6):1938-1951. doi: 10.1007/s43032-022-01133-4. Epub 2022 Dec 20.

Abstract

As one of the factors of male infertility, high temperature induces apoptosis of differentiated spermatogenic cells, sperm DNA oxidative damage, and changes in morphology and function of Sertoli cells. Spermatogonial stem cells (SSCs) are a type of germline stem cells that maintain spermatogenesis through self-renewal and differentiation. At present, however, the effect of high temperature on SSC differentiation remains unknown. In this study, an in vitro SSC differentiation model was used to investigate the effect of heat stress treatment on SSC differentiation, and RNA sequencing (RNA-seq) was used to enrich the key genes and pathways in high temperature inhibiting SSC differentiation. Results show that 2 days of 37 °C or 43 °C (30 min per day) heat stress treatment significantly inhibited SSC differentiation. The differentiation-related genes c-kit, stra8, Rec8, Sycp3, and Ovol1 were down-regulated after 2 and 4 days of heat stress at 37 °C. The transcriptome of SSCs was significantly differentially expressed on days 2 and 4 after heat stress treatment at 37 °C. In total, 1660 and 7252 differentially expressed genes (DEGs) were identified by RNA-seq in SSCs treated with heat stress at 37 °C for 2 and 4 days, respectively. KEGG pathway analysis showed that p53, ribosome, and carbon metabolism signaling pathways promoting stem cell differentiation were significantly enriched after heat stress treatment at 37 °C. In conclusion, 37 °C significantly inhibited SSC differentiation, and p53, ribosome, and carbon metabolism signaling pathways were involved in this differentiation inhibition process. The results of this study provide a reference for further investigation into the mechanism by which high temperature inhibits SSC differentiation.

摘要

作为男性不育症的因素之一,高温会诱导分化的精原细胞凋亡、精子 DNA 氧化损伤以及支持细胞的形态和功能发生变化。精原干细胞(SSC)是一种生殖细胞干细胞,通过自我更新和分化维持精子发生。然而,目前高温对 SSC 分化的影响尚不清楚。在本研究中,我们使用体外 SSC 分化模型来研究热应激处理对 SSC 分化的影响,并通过 RNA 测序(RNA-seq)富集高温抑制 SSC 分化的关键基因和通路。结果表明,37°C 或 43°C(每天 30 分钟)的 2 天热应激处理显著抑制了 SSC 的分化。在 37°C 下热应激处理 2 天和 4 天后,分化相关基因 c-kit、stra8、Rec8、Sycp3 和 Ovol1 下调。热应激处理 2 天和 4 天后,SSC 的转录组发生明显差异表达。总共在 37°C 热应激处理 2 天和 4 天后的 SSCs 中鉴定出 1660 和 7252 个差异表达基因(DEGs)。KEGG 通路分析表明,p53、核糖体和碳代谢信号通路促进干细胞分化在 37°C 热应激处理后显著富集。总之,37°C 显著抑制 SSC 的分化,p53、核糖体和碳代谢信号通路参与了这一分化抑制过程。本研究结果为进一步研究高温抑制 SSC 分化的机制提供了参考。

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