Gene regulation and signaling transduction in mediating the self-renewal, differentiation, and apoptosis of spermatogonial stem cells.

Asian journal of andrology Pub Date : 2025-01-01 Epub Date: 2024-08-20 DOI:10.4103/aja202464
Cai-Mei He, Dong Zhang, Zuping He
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引用次数: 0

Abstract

Abstract: Infertility has become one of the most serious diseases worldwide, and 50% of this disease can be attributed to male-related factors. Spermatogenesis, by definition, is a complex process by which spermatogonial stem cells (SSCs) self-renew to maintain stem cell population within the testes and differentiate into mature spermatids. It is of great significance to uncover gene regulation and signaling pathways that are involved in the fate determinations of SSCs with aims to better understand molecular mechanisms underlying human spermatogenesis and identify novel targets for gene therapy of male infertility. Significant achievement has recently been made in demonstrating the signaling molecules and pathways mediating the fate decisions of mammalian SSCs. In this review, we address key gene regulation and crucial signaling transduction pathways in controlling the self-renewal, differentiation, and apoptosis of SSCs, and we illustrate the networks of genes and signaling pathways in SSC fate determinations. We also highlight perspectives and future directions in SSC regulation by genes and their signaling pathways. This review could provide novel insights into the genetic regulation of normal and abnormal spermatogenesis and offer molecular targets to develop new approaches for gene therapy of male infertility.

介导精原干细胞自我更新、分化和凋亡的基因调控和信号转导。
不育症已成为全球最严重的疾病之一,其中50%可归因于与男性有关的因素。根据定义,精子发生是精原干细胞(SSC)自我更新以维持睾丸内干细胞群并分化为成熟精子的复杂过程。揭示参与精原干细胞命运决定的基因调控和信号通路,对于更好地理解人类精子发生的分子机制和确定男性不育症基因治疗的新靶点具有重要意义。近来,在证明介导哺乳动物造精细胞命运决定的信号分子和通路方面取得了重大成就。在这篇综述中,我们探讨了控制造血干细胞自我更新、分化和凋亡的关键基因调控和重要信号转导途径,并阐述了造血干细胞命运决定过程中的基因和信号途径网络。我们还强调了基因及其信号通路对造血干细胞调控的前景和未来方向。本综述可为正常和异常精子发生的基因调控提供新的见解,并为开发男性不育基因治疗的新方法提供分子靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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