National Chengdu Center for Safety Evaluation of Drugs and National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu 610041, People's Republic of China.
Department of Pathology, West China Hospital, Sichuan University, Chengdu 610041, People's Republic of China.
Int J Nanomedicine. 2020 Nov 27;15:9499-9514. doi: 10.2147/IJN.S276606. eCollection 2020.
Gold nanoparticles (AuNPs) have shown great promise in various biomedical applications, but their effects on male reproductive function remain to be ascertained. The aim of this study was to investigate the uptake, cytotoxicity and testosterone production inhibition of AuNPs in mouse Leydig cells, as well as their accumulation in the testes of male mice and their effects on male reproductive function.
AuNPs (5 nm) were able to be internalized into the endosomes/lysosomes of TM3 Leydig cells, induce the formation of autophagosomes, increase the production of reactive oxygen species (ROS), and disrupt the cell cycle in S phase, resulting in concentration-dependent cytotoxicity and DNA damage. Interestingly, AuNPs significantly reduced testosterone production in TM3 cells by inhibiting the expression of 17α-hydroxylase, an important enzyme in androgen synthesis. After repeated intravenous injection, AuNPs gradually accumulated and retained in the testes of male BALB/c mice in a dose-dependent manner. One week after withdrawal, the level of plasma testosterone in the 0.5 mg/kg AuNPs group was significantly reduced compared to that in the PBS control group, accompanied by the decreased expression of 17α-hydroxylase in the testes. In addition, AuNPs treatment significantly increased the rate of epididymal sperm malformation, but without affecting fertility.
Our results suggest that AuNPs can accumulate in the testes and reduce testosterone production in Leydig cells by down-regulating the expression of 17α-hydroxylase, thus affecting the quality of epididymal sperm.
金纳米粒子(AuNPs)在各种生物医学应用中表现出巨大的潜力,但它们对男性生殖功能的影响仍需确定。本研究旨在探讨 AuNPs 在小鼠睾丸间质细胞中的摄取、细胞毒性和睾酮产生抑制作用,以及它们在雄性小鼠睾丸中的积累及其对雄性生殖功能的影响。
5nm 的 AuNPs 能够被 TM3 睾丸间质细胞内吞进入内体/溶酶体,诱导自噬体的形成,增加活性氧(ROS)的产生,并破坏 S 期细胞周期,导致浓度依赖性的细胞毒性和 DNA 损伤。有趣的是,AuNPs 通过抑制雄激素合成的重要酶 17α-羟化酶的表达,显著降低 TM3 细胞中的睾酮产生。经重复静脉注射后,AuNPs 逐渐以剂量依赖性方式在雄性 BALB/c 小鼠的睾丸中积累和保留。在停止注射 AuNPs 1 周后,0.5mg/kg AuNPs 组的血浆睾酮水平与 PBS 对照组相比显著降低,同时睾丸中 17α-羟化酶的表达也降低。此外,AuNPs 处理显著增加了附睾精子畸形的发生率,但不影响生育能力。
我们的结果表明,AuNPs 可以在睾丸中积累,并通过下调 17α-羟化酶的表达降低睾丸间质细胞中的睾酮产生,从而影响附睾精子的质量。