Xing Huilin, Chen Shu, Wang Mingxia, Zheng Tingting, Yang Bo
Shenzhen Key Laboratory for Drug Addiction and Medication Safety, Peking University Shenzhen Hospital, Shenzhen Peking University‑Hong Kong University of Science and Technology Medical Center, Shenzhen, Guangdong 518036, P.R. China.
The Reproductive Medicine Center, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Mol Med Rep. 2025 Oct;32(4). doi: 10.3892/mmr.2025.13634. Epub 2025 Jul 25.
Infertility is a multifactorial condition that affects ~7% of the male population. The mechanism of male infertility primarily involves intrinsic and environmental factors, of which genetic defects are key for its occurrence. Sirtuin 5 (SIRT5) is primarily localized in mitochondria and associated with male reproduction. SIRT5 is downregulated in asthenozoospermic sperm compared with normal sperm. To explore the role of SIRT5 in male reproduction, Cell Counting Kit‑8, EdU, wound healing, and apoptosis assayswere performed in GC‑2 spd cells (mouse spermatocytes) which revealed that SIRT5 inhibited apoptosis and promoted cell proliferation and migration. Western blotting was performed and the results showed that SIRT5 was involved in the proliferation of GC‑2 spd cells by regulating the PI3K/AKT signaling pathway. The present study demonstrated a mechanism of male infertility, which may aid in its treatment.
不育是一种多因素疾病,影响约7%的男性人群。男性不育的机制主要涉及内在因素和环境因素,其中遗传缺陷是其发生的关键。沉默调节蛋白5(SIRT5)主要定位于线粒体,与男性生殖有关。与正常精子相比,SIRT5在弱精子症精子中表达下调。为了探究SIRT5在男性生殖中的作用,在GC-2 spd细胞(小鼠精母细胞)中进行了细胞计数试剂盒-8、EdU、伤口愈合和凋亡检测,结果显示SIRT5抑制凋亡并促进细胞增殖和迁移。进行了蛋白质免疫印迹分析,结果表明SIRT5通过调节PI3K/AKT信号通路参与GC-2 spd细胞的增殖。本研究揭示了一种男性不育的机制,可能有助于其治疗。