Department of Physiology, School of Basic Medical Sciences, Nanchang University, Nanchang, China.
Nanchang Emergency Center, Nanchang, China.
Environ Toxicol. 2022 Nov;37(11):2756-2763. doi: 10.1002/tox.23634. Epub 2022 Aug 3.
Lysophosphatidylcholine (LPC), a major class of glycerophospholipids ubiquitously present in most tissues, plays a dominant role in many diseases, while it is still unknown about the potential mechanism of LPC affecting the testicular Leydig cells. In the present study, mouse TM3 Leydig cells in vitro were treated with LPC for 48 h. LPC was found to significantly induce apoptosis and oxidative stress of mouse TM3 Leydig cells; while inhibition of oxidative stress by N-acetyl-L-cysteine, an inhibitor of oxidative stress, could rescue the induction of apoptosis, indicating that LPC induced apoptosis of mouse TM3 Leydig cells via oxidative stress. Interestingly, LPC was showed to inhibit autophagy; however, induction of autophagy by rapamycin significantly alleviated the induction of apoptosis by LPC. Taken together, oxidative stress was involved in LPC-induced apoptosis of mouse TM3 Leydig cells, and autophagy might play a protective role in LPC-induced apoptosis.
溶血磷脂胆碱(LPC)是一种广泛存在于大多数组织中的甘油磷脂的主要类别,在许多疾病中发挥着主导作用,而关于 LPC 影响睾丸间质细胞的潜在机制尚不清楚。在本研究中,用 LPC 处理体外 TM3 间质细胞 48 小时。发现 LPC 可显著诱导 TM3 间质细胞凋亡和氧化应激;而抗氧化应激抑制剂 N-乙酰-L-半胱氨酸可挽救诱导的凋亡,表明 LPC 通过氧化应激诱导 TM3 间质细胞凋亡。有趣的是,LPC 被显示抑制自噬;然而,雷帕霉素诱导的自噬明显减轻了 LPC 诱导的凋亡。总之,氧化应激参与了 LPC 诱导的 TM3 间质细胞凋亡,自噬可能在 LPC 诱导的凋亡中起保护作用。