Department of Urology, Gongli Hospital of Shanghai Pudong New Area, Shanghai, China.
School of Medicine, Qingdao University, Qingdao, China.
Am J Reprod Immunol. 2024 Jan;91(1):e13811. doi: 10.1111/aji.13811.
Male infertility is a common disease affecting male reproductive health. Leptin is an important hormone that regulates various physiological processes, including reproductive function. However, few experimental studies have been carried out to elucidate the mechanism of leptin's effects on male reproductive function.
The purpose of this study was to investigate the effects of leptin on testicular spermatogenesis and its mechanism, so as to provide potential targets for the treatment of patients with spermatogenic dysfunction.
Testicular tissues were collected from eight prostate cancer patients undergoing surgical castration. GPR125-positive spermatogonia were isolated by two consecutive magnetic activated cell sorting (MACS), followed by incubation with conditioned medium. To identify the signaling pathway(s) involved in the effects of leptin, undifferentiated spermatogonia were treated with different concentrations of leptin and antagonists of leptin-related pathways. The proliferative effect of leptin was evaluated by cell counting using a hemocytometer. Expressions of p-AKT, p-ERK, p-STAT, and p-S6K were determined by western blotting analysis.
Leptin promoted the growth of human GPR125-positive spermatogonia in a concentration-dependent manner. The most significant proliferative effect was observed using 100 ng/mL leptin after 6 days of culture. Leptin significantly increased the phosphorylation of STAT3, AKT, and ERK in undifferentiated spermatogonia. Phosphatidylinositol 3-kinase (PI3K) inhibitor LY294002 inhibited the leptin-induced activation of AKT, ERK, and downstream S6K. Treatment with the mammalian target of rapamycin (mTOR) inhibitor rapamycin also inhibited S6K phosphorylation. Moreover, both LY294002 and rapamycin were found to inhibit the leptin-induced proliferation of undifferentiated spermatogonia. These results suggested that the leptin-induced proliferation of GPR125-positive spermatogonia was dependent on the PI3K/AKT/mTOR pathway. Further exploration of proliferation and apoptotic markers suggested that leptin may alleviate cell apoptosis by regulating the expression of Bax and FasL.
A certain concentration of leptin (25∼100 ng/mL) could promote proliferation of undifferentiated spermatogonia, which was mediated by PI3K/AKT/mTOR pathway.
男性不育是一种常见的影响男性生殖健康的疾病。瘦素是一种重要的激素,它调节着包括生殖功能在内的各种生理过程。然而,很少有实验研究阐明瘦素对男性生殖功能的影响机制。
本研究旨在探讨瘦素对睾丸生精功能的影响及其机制,为治疗生精功能障碍患者提供潜在靶点。
收集 8 例行手术去势的前列腺癌患者的睾丸组织。通过连续两次磁激活细胞分选(MACS)分离 GPR125 阳性精原细胞,然后用条件培养基孵育。为了鉴定瘦素作用涉及的信号通路,用不同浓度的瘦素和瘦素相关通路的拮抗剂处理未分化的精原细胞。用血细胞计数器评估瘦素的增殖作用。通过 Western blot 分析测定 p-AKT、p-ERK、p-STAT 和 p-S6K 的表达。
瘦素以浓度依赖的方式促进人 GPR125 阳性精原细胞的生长。培养 6 天后,使用 100ng/mL 的瘦素可观察到最显著的增殖效果。瘦素显著增加了未分化精原细胞中 STAT3、AKT 和 ERK 的磷酸化。磷脂酰肌醇 3-激酶(PI3K)抑制剂 LY294002 抑制了瘦素诱导的 AKT、ERK 和下游 S6K 的激活。使用雷帕霉素(mTOR)抑制剂 rapamycin 处理也抑制了 S6K 的磷酸化。此外,LY294002 和 rapamycin 均能抑制瘦素诱导的未分化精原细胞增殖。这些结果表明,瘦素诱导 GPR125 阳性精原细胞的增殖依赖于 PI3K/AKT/mTOR 通路。进一步探索增殖和凋亡标志物表明,瘦素可能通过调节 Bax 和 FasL 的表达来减轻细胞凋亡。
一定浓度的瘦素(25∼100ng/mL)可促进未分化精原细胞增殖,这是由 PI3K/AKT/mTOR 通路介导的。