Maroto María, Torvisco Sara N, García-Merino Cristina, Fernández-González Raúl, Pericuesta Eva
National Institute for Agricultural and Food Research and Technology (INIA-CSIC), 28040 Madrid, Spain.
School of Agriculture and Food Science, University College Dublin, D04 W6F6 Dublin, Ireland.
Biomolecules. 2025 Mar 29;15(4):500. doi: 10.3390/biom15040500.
Spermatogenesis is a complex and highly regulated process involving the proliferation, differentiation, and apoptosis of germ cells. This process is controlled by various hormonal, genetic, and environmental factors, including temperature. In hormonal regulation, follicle-stimulating hormone (FSH), luteinizing hormone (LH), and testosterone (T) are essential for correct spermatogenesis development from the early stages and spermatogonia proliferation to germ cell maturation. Other hormones, like inhibin and activin, finely participate tuning the process of spermatogenesis. Genetic regulation involves various transcription factors, such as , , and , which are crucial for the development and maintenance of the testis and germ cells. MicroRNAs (miRNAs) play a significant role by regulating gene expression post-transcriptionally. Epigenetic modifications, including DNA methylation, histone modifications, and chromatin remodelling, are also vital. Temperature regulation is another critical aspect, with the testicular temperature maintained around 2-4 °C below body temperature, essential for efficient spermatogenesis. Heat shock proteins (HSPs) protect germ cells from heat-induced damage by acting as molecular chaperones, ensuring proper protein folding and preventing the aggregation of misfolded proteins during thermal stress. Elevated testicular temperature can impair spermatogenesis, increasing germ cell apoptosis and inducing oxidative stress, DNA damage, and the disruption of the blood-testis barrier, leading to germ cell death and impaired differentiation. The cellular mechanisms of germ cell proliferation, differentiation, and death include the mitotic divisions of spermatogonia to maintain the germ cell pool and produce spermatocytes. Spermatocytes undergo meiosis to produce haploid spermatids, which then differentiate into mature spermatozoa. Apoptosis, or programmed cell death, ensures the removal of defective germ cells and regulates the germ cell population. Hormonal imbalance, genetic defects, and environmental stress can trigger apoptosis during spermatogenesis. Understanding these mechanisms is crucial for addressing male infertility and developing therapeutic interventions. Advances in molecular biology and genetics continue to uncover the intricate details of how spermatogenesis is regulated at multiple levels, providing new insights and potential targets for treatment.
精子发生是一个复杂且高度受调控的过程,涉及生殖细胞的增殖、分化和凋亡。这个过程受多种激素、遗传和环境因素控制,包括温度。在激素调节中,促卵泡生成素(FSH)、黄体生成素(LH)和睾酮(T)对于从早期阶段正确的精子发生发育以及精原细胞增殖到生殖细胞成熟至关重要。其他激素,如抑制素和激活素,精细地参与调节精子发生过程。遗传调控涉及多种转录因子,如 、 和 ,它们对于睾丸和生殖细胞的发育及维持至关重要。微小RNA(miRNA)通过转录后调控基因表达发挥重要作用。表观遗传修饰,包括DNA甲基化、组蛋白修饰和染色质重塑,也至关重要。温度调节是另一个关键方面,睾丸温度维持在比体温低约2 - 4°C,这对高效精子发生至关重要。热休克蛋白(HSP)作为分子伴侣保护生殖细胞免受热诱导损伤,确保蛋白质正确折叠并防止热应激期间错误折叠蛋白质的聚集。睾丸温度升高会损害精子发生,增加生殖细胞凋亡并诱导氧化应激、DNA损伤以及血睾屏障破坏,导致生殖细胞死亡和分化受损。生殖细胞增殖、分化和死亡的细胞机制包括精原细胞的有丝分裂以维持生殖细胞库并产生精母细胞。精母细胞进行减数分裂产生单倍体精子细胞,然后分化为成熟精子。凋亡,即程序性细胞死亡,确保清除有缺陷的生殖细胞并调节生殖细胞数量。激素失衡、遗传缺陷和环境应激可在精子发生过程中触发凋亡。了解这些机制对于解决男性不育问题和开发治疗干预措施至关重要。分子生物学和遗传学的进展不断揭示精子发生在多个层面如何被调控的复杂细节,为治疗提供新的见解和潜在靶点。