Zhang Ping, Zhang Longsheng, Yu Li, Zhou Xinli, Chen Xu, Zhou Yuchuan, Wang Ningling, Zhu Hui
International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Shanghai Key Laboratory of Embryo Original Diseases, Shanghai, China.
Andrology. 2025 Oct;13(7):1901-1912. doi: 10.1111/andr.13800. Epub 2024 Nov 17.
Mammalian spermatogenesis is a highly complex process of cell proliferation, meiosis, and differentiation. A series of genes are expressed in an orderly and precise manner to ensure spermatogenesis, with chromatin undergoing intricate changes throughout. EP300-interacting inhibitor of differentiation 3 (Eid3) is a testis-enriched gene, but its role in male reproduction remains unclear.
To investigate the role of EID3 in male spermatogenesis and explore the potential underlying mechanism.
We generated Eid3 knockout mouse model using the CRISPR-Cas9 system. We measured the expression of EID3 in mouse tissues and testicular cell populations by qRT-PCR and western blot. Histological analysis, including hematoxylin and eosin (H&E) and periodic acid-Schiff (PAS) staining, together with computer-assisted sperm analysis (CASA), were performed to evaluate the effect of EID3 on spermatogenesis in mice. Light and ultrastructural microscopy were used to evaluate the morphology and structure of the Eid3 spermatozoa. We used western blot and immunofluorescence to further analyze the function of EID3 in spermiogenesis.
Eid3 mouse showed a significant decrease in sperm count, motility, and morphology. Loss of EID3 impaired the normal meiotic process and induced apoptosis of abnormally developing spermatocytes, ultimately resulting in the decrease of sperm cell number. Additionally, EID3 deficiency led to a decrease in histone acetylation levels in spermatids, impaired histone-to-protamine transition and chromatin condensation process, and ultimately resulted in abnormal sperm morphology.
This study confirms for the first time that EID3 is crucial for meiosis and chromatin condensation during spermatogenesis, and EID3 deficiency leads to a significant decrease in sperm parameters. Given the high expression paradigm of Eid3 in human testis, EID3 likely plays a role in human reproduction. Future research could provide a new target for the clinical diagnosis and treatment of male infertility.
哺乳动物精子发生是一个涉及细胞增殖、减数分裂和分化的高度复杂过程。一系列基因以有序且精确的方式表达以确保精子发生,在此过程中染色质经历复杂变化。EP300相互作用分化抑制因子3(Eid3)是一个睾丸富集基因,但其在雄性生殖中的作用尚不清楚。
研究EID3在雄性精子发生中的作用并探索其潜在机制。
我们使用CRISPR-Cas9系统构建了Eid3基因敲除小鼠模型。通过qRT-PCR和蛋白质免疫印迹法检测小鼠组织和睾丸细胞群体中EID3的表达。进行组织学分析,包括苏木精-伊红(H&E)染色和过碘酸-希夫(PAS)染色,并结合计算机辅助精子分析(CASA)来评估EID3对小鼠精子发生的影响。利用光学和超微结构显微镜评估Eid3基因敲除小鼠精子的形态和结构。我们通过蛋白质免疫印迹法和免疫荧光进一步分析EID3在精子形成中的功能。
Eid3基因敲除小鼠的精子数量、活力和形态显著下降。EID3缺失破坏了正常的减数分裂过程,诱导异常发育的精母细胞凋亡,最终导致精子细胞数量减少。此外,EID3缺乏导致精子细胞中组蛋白乙酰化水平降低,损害组蛋白向鱼精蛋白的转变以及染色质凝聚过程,最终导致精子形态异常。
本研究首次证实EID3在精子发生过程中的减数分裂和染色质凝聚中起关键作用,EID3缺乏导致精子参数显著下降。鉴于Eid3在人类睾丸中的高表达模式,EID3可能在人类生殖中发挥作用。未来的研究可为男性不育症的临床诊断和治疗提供新靶点。