External pressure induced the dysfunction of Sertoli cells via the Fas/FasL signaling pathway.

IF 2.1 4区 医学 Q3 ANDROLOGY
Yuxin Liu, Houtao Long, Qihao Sun, Daofeng Zhang, Junhao Zheng, Haiyang Zhang
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引用次数: 0

Abstract

Cryptorchidism, a condition where the testis fails to fully descend into the scrotum during development, is associated with elevated environmental temperatures and pressures, leading to male infertility and germ cell tumors. Factors such as oxidative stress and high temperatures contribute to infertility in cryptorchidism. This study aims to explore how external pressure affects Sertoli cells and discover new mechanisms affecting spermatogenesis in cryptorchidism. Sertoli cells were subjected to various pressure levels (0 mmHg, 25 mmHg, 50 mmHg, 100 mmHg) and durations (0 h, 2 h, 4 h) using an enzyme-linked immunosorbent assay (ELISA) to measure androgen binding protein (ABP) and inhibin B (INH B) secretion. Cell morphology changes were observed using immunofluorescence; apoptosis rates were measured with terminal-deoxynucleotidyl transferase mediated nick end labelling (TUNEL) assay and flow cytometry; ultrastructural variations were examined via transmission electron microscopy; and the expression of apoptosis-related proteins (Fas, FasL, caspase 3, and caspase 8) was analyzed through immunohistochemistry, real-time polymerase chain reaction (real-time PCR), and western blotting. The results showed that elevated pressure suppressed ABP and INH B secretion from Sertoli cells. Structural changes were observed under pressure, including cytoskeleton loosening and nuclear fragmentation. Apoptosis rates increased with higher pressure levels. Ultrastructural analysis revealed chromatin changes, apoptotic bodies, and mitochondrial alterations. Increased expressions of Fas and FasL were detected, along with elevated levels of caspase 3 and caspase 8. The caspase 8 inhibitor blocked pressure-induced apoptosis and caspase 3 activation, while the cytochrome C inhibitor did not show the same effect. Our findings suggested that external pressure induces apoptosis of Sertoli cells via the Fas/FasL signaling pathway, potentially contributing to male infertility associated with cryptorchidism.

外部压力通过 Fas/FasL 信号通路诱发了 Sertoli 细胞的功能障碍。
隐睾症是指睾丸在发育过程中未能完全下降到阴囊内,与环境温度和压力升高有关,导致男性不育和生殖细胞肿瘤。氧化应激和高温等因素导致隐睾症患者不育。本研究旨在探索外部压力如何影响 Sertoli 细胞,并发现影响隐睾症精子发生的新机制。使用酶联免疫吸附试验(ELISA)测量雄激素结合蛋白(ABP)和抑制素B(INH B)的分泌情况,对Sertoli细胞施加不同的压力水平(0毫米汞柱、25毫米汞柱、50毫米汞柱、100毫米汞柱)和持续时间(0小时、2小时、4小时)。免疫荧光法观察细胞形态变化;末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)和流式细胞术测量细胞凋亡率;透射电子显微镜检查超微结构变化;免疫组化、实时聚合酶链反应(real-time PCR)和免疫印迹法分析细胞凋亡相关蛋白(Fas、FasL、caspase 3 和 caspase 8)的表达。结果显示,压力升高抑制了 Sertoli 细胞分泌 ABP 和 INH B。在压力下可观察到结构变化,包括细胞骨架松动和核破碎。细胞凋亡率随压力水平升高而增加。超微结构分析揭示了染色质变化、凋亡体和线粒体改变。检测到 Fas 和 FasL 表达增加,caspase 3 和 caspase 8 水平升高。caspase 8抑制剂阻止了压力诱导的细胞凋亡和caspase 3的激活,而细胞色素C抑制剂没有显示出同样的效果。我们的研究结果表明,外部压力可通过Fas/FasL信号通路诱导Sertoli细胞凋亡,这可能是隐睾症导致男性不育的原因之一。
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来源期刊
CiteScore
4.30
自引率
4.20%
发文量
27
审稿时长
>12 weeks
期刊介绍: Systems Biology in Reproductive Medicine, SBiRM, publishes Research Articles, Communications, Applications Notes that include protocols a Clinical Corner that includes case reports, Review Articles and Hypotheses and Letters to the Editor on human and animal reproduction. The journal will highlight the use of systems approaches including genomic, cellular, proteomic, metabolomic, bioinformatic, molecular, and biochemical, to address fundamental questions in reproductive biology, reproductive medicine, and translational research. The journal publishes research involving human and animal gametes, stem cells, developmental biology and toxicology, and clinical care in reproductive medicine. Specific areas of interest to the journal include: male factor infertility and germ cell biology, reproductive technologies (gamete micro-manipulation and cryopreservation, in vitro fertilization/embryo transfer (IVF/ET) and contraception. Research that is directed towards developing new or enhanced technologies for clinical medicine or scientific research in reproduction is of significant interest to the journal.
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