EP300-interacting inhibitor of differentiation 3 is required for spermatogenesis in mice.

IF 3.2 2区 医学 Q1 ANDROLOGY Andrology Pub Date : 2024-11-17 DOI:10.1111/andr.13800
Ping Zhang, Longsheng Zhang, Li Yu, Xinli Zhou, Xu Chen, Yuchuan Zhou, Ningling Wang, Hui Zhu
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Abstract

Background: 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.

Objective: To investigate the role of EID3 in male spermatogenesis and explore the potential underlying mechanism.

Materials and methods: 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.

Results: 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.

Discussion and conclusions: 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.

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小鼠精子发生需要 EP300 交互作用分化抑制因子 3。
背景:哺乳动物的精子发生是一个非常复杂的过程,包括细胞增殖、减数分裂和分化。一系列基因以一种有序而精确的方式表达,以确保精子发生,染色质在整个过程中发生着复杂的变化。EP300相互作用分化抑制因子3(Eid3)是一种睾丸富集基因,但其在男性生殖中的作用仍不清楚:研究EID3在男性精子发生中的作用,并探索其潜在的内在机制:我们利用CRISPR-Cas9系统建立了EID3基因敲除小鼠模型。通过qRT-PCR和Western blot检测EID3在小鼠组织和睾丸细胞群中的表达。为了评估EID3对小鼠精子发生的影响,我们进行了组织学分析,包括苏木精和伊红(H&E)染色、周期性酸-Schiff(PAS)染色以及计算机辅助精子分析(CASA)。光镜和超微结构镜用于评估Eid3-/-精子的形态和结构。我们利用Western印迹和免疫荧光进一步分析了EID3在精子发生中的功能:结果:Eid3-/-小鼠的精子数量、活力和形态均显著下降。结果:EID3-/-小鼠的精子数量、活力和形态均明显下降,EID3缺失会影响正常的减数分裂过程,并诱导发育异常的精母细胞凋亡,最终导致精子细胞数量减少。此外,EID3的缺乏导致精子中组蛋白乙酰化水平下降,组蛋白向质粒转化和染色质凝聚过程受损,最终导致精子形态异常:本研究首次证实了EID3对精子发生过程中的减数分裂和染色质凝集至关重要,EID3缺乏会导致精子参数显著下降。鉴于EID3在人类睾丸中的高表达范例,EID3很可能在人类生殖过程中发挥作用。未来的研究可能会为男性不育症的临床诊断和治疗提供一个新的靶点。
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来源期刊
Andrology
Andrology ANDROLOGY-
CiteScore
9.10
自引率
6.70%
发文量
200
期刊介绍: Andrology is the study of the male reproductive system and other male gender related health issues. Andrology deals with basic and clinical aspects of the male reproductive system (gonads, endocrine and accessory organs) in all species, including the diagnosis and treatment of medical problems associated with sexual development, infertility, sexual dysfunction, sex hormone action and other urological problems. In medicine, Andrology as a specialty is a recent development, as it had previously been considered a subspecialty of urology or endocrinology
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