E2F1在隐睾小鼠中促进EIF4EBP1转录的作用:与生殖细胞自噬的关联

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY
Frontiers in Genetics Pub Date : 2025-05-23 eCollection Date: 2025-01-01 DOI:10.3389/fgene.2025.1536672
Jianguo Zhang, Yanhui Liu, Hailong Zhang, Lin Yang, Danjing Sun, Lili Xiao, Xiaoyun Wang, Xiangming Wu
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引用次数: 0

摘要

隐睾症可引起生殖细胞过度自噬和凋亡,从而影响生育能力。本研究探讨了E2F1在隐睾中调控EIF4EBP1表达的作用及其在隐睾过度自噬和凋亡中的作用。方法:采用手术干预法建立小鼠隐睾模型,热应激法建立体外隐睾精原细胞模型。通过逆转录定量聚合酶链反应(RT-qPCR)和Western blotting检测EIF4EBP1及自噬和凋亡相关关键蛋白的表达水平,通过HE染色和Masson染色评估睾丸损伤和纤维化。测定血清和睾丸睾酮水平,以及氧化应激标志物。双荧光素酶报告基因检测和ChIP证实了E2F1对EIF4EBP1的调控作用。通过调控EIF4EBP1的表达,进一步分析了E2F1和EIF4EBP1对睾丸损伤、细胞凋亡和自噬的影响。结果:在隐睾小鼠模型中,观察到睾丸体积和重量减少,睾丸损伤和纤维化增加,睾酮水平下降,精子数量和活力受损。体外隐睾精原细胞模型细胞活力降低,氧化应激升高。在这些模型中,自噬和细胞凋亡均加重。EIF4EBP1表达上调,其敲低可改善不良反应。E2F1被鉴定为EIF4EBP1的上游调控因子,敲低E2F1可显著降低EIF4EBP1启动子的活性和结合。用HLM006474抑制E2F1降低了EIF4EBP1的表达,而EIF4EBP1过表达加重了自噬和细胞凋亡。结论:E2F1在隐睾中调控EIF4EBP1的表达,导致隐睾细胞过度自噬和凋亡。抑制E2F1可减少这些病理过程,减轻睾丸损伤,提高生育能力,突出了隐睾的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of E2F1 in promoting EIF4EBP1 transcription in cryptorchid mice: association with autophagy in germ cells.

Introduction: Cryptorchidism can cause excessive germ cell autophagy and apoptosis to impair fertility. This study investigates the role of E2F1 in regulating EIF4EBP1 expression and its contribution to excessive autophagy and apoptosis in cryptorchidism.

Methods: A cryptorchidism mouse model was established through surgical intervention, while an in vitro cryptorchid spermatogonial cell model was created using heat stress. Expression levels of EIF4EBP1 and key proteins involved in autophagy and apoptosis were assessed by reverse transcription quantitative polymerase chain reaction (RT-qPCR) and Western blotting Testicular damage and fibrosis were evaluated through HE staining and Masson staining. Serum and testicular testosterone levels were measured, alongside markers of oxidative stress. The regulatory role of E2F1 on EIF4EBP1 was confirmed by dual-luciferase reporter assays and ChIP. Further analysis of the effects of E2F1 and EIF4EBP1 on testicular damage, apoptosis, and autophagy was performed by manipulating EIF4EBP1 expression.

Results: In the cryptorchidism mouse model, reduced testicular volume and weight, increased testicular damage and fibrosis, decreased testosterone levels, and impaired sperm count and vitality were observed. In the in vitro cryptorchid spermatogonial cell model, cell viability was reduced, while oxidative stress was elevated. Both autophagy and apoptosis were exacerbated in these models. EIF4EBP1 expression was upregulated, and its knockdown ameliorated the adverse effects. E2F1 was identified as an upstream regulator of EIF4EBP1, with knockdown of E2F1 significantly decreasing EIF4EBP1 promoter activity and binding. Inhibition of E2F1 using HLM006474 reduced EIF4EBP1 expression, while EIF4EBP1 overexpression aggravated autophagy and apoptosis.

Conclusion: E2F1 regulates EIF4EBP1 expression in cryptorchidism, contributing to excessive autophagy and apoptosis. Inhibiting E2F1 reduces these pathological processes, alleviating testicular damage and improving fertility, highlighting potential therapeutic targets for cryptorchidism.

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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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