Effect of MEHP on testosterone synthesis via Sirt1/Foxo1/Rab7 signaling pathway inhibition of lipophagy in TM3 cells

• Published in: Ecotoxicology and environmental safety 2024-06, Vol.277, p.116394-116394, Article 116394
• Main Authors: Hao, Yu, Tian, Xuan'en, Yan, Fengmei, Wang, Xiuqin, Huang, Jing, Li, Ling
• Format: Article
• Language: English
• Subjects: Animals; Cell Line; Cholesterol; Diethylhexyl Phthalate - analogs & derivatives; Diethylhexyl Phthalate - toxicity; Forkhead Box Protein O1 - metabolism; Foxo1; Lipophagy; Mice; Mono-2-ethylhexyl phthalic acid; Plasticizers - toxicity; rab GTP-Binding Proteins - metabolism; Rab7; rab7 GTP-Binding Proteins; Signal Transduction - drug effects; Sirt1; Sirtuin 1 - metabolism; Testosterone
• ISSN: 0147-6513; 1090-2414
• DOI: 10.1016/j.ecoenv.2024.116394

Mono-2-ethylhexyl phthalic acid (MEHP) is the most toxic metabolite of the plasticizer di-2-ethylhexyl phthalic acid (DEHP), and studies have shown that MEHP causes serious reproductive effects. However, its exact mechanisms of action remain elusive. In this study, we aimed to investigate the reproductive effects of MEHP and preliminarily explore its underlying molecular mechanisms. We found that TM3 cells gradually secreted less testosterone and intracellular free cholesterol with increasing MEHP exposure. MEHP exposure inhibited lipophagy and the Sirt1/Foxo1/Rab7 signaling pathway in TM3 cells, causing aberrant accumulation of intracellular lipid droplets. Addition of the Sirt1 agonist SRT1720 and Rab7 agonist ML-098 alleviated the inhibition of lipophagy and increased free cholesterol and testosterone contents in TM3 cells. SRT1720 alleviated the inhibitory effect of MEHP on the Sirt1/Foxo1/Rab7 signaling pathway, whereas ML-098 only alleviated the inhibition of Rab7 protein expression by MEHP and had no effect on Sirt1 and Foxo1 protein expression. This suggests that MEHP inhibits lipophagy in TM3 cells by suppressing the Sirt1/Foxo1/Rab7 signaling pathway, ultimately leading to a further decrease in cellular testosterone secretion. This study improves our current understanding of the toxicity and molecular mechanisms of action of MEHP and provides new insights into the reproductive effects of phthalic acid esters. [Display omitted] •Lipophagy played a key role in MEHP-induced testosterone biosynthesis disruption in TM3 cell.•MEHP inhibits lipophagy in TM3 cells by suppressing the Sirt1/Foxo1/Rab7 signaling pathway.•Pretreatment with Sirt1 agonist SRT1720 and Rab7 agonist ML-098 attenuates MEHP-induced testosterone synthesis reduction.