Integrated RNA sequencing and biochemical studies reveal endoplasmic reticulum stress and autophagy dysregulation contribute to Tri (2-Ethylhexyl) phosphate (TEHP)-induced cell injury in Sertoli cells

Environ Pollut. 2024 Nov 1:360:124536. doi: 10.1016/j.envpol.2024.124536. Epub 2024 Jul 17.

Abstract

Tri (2-Ethylhexyl) phosphate (TEHP), widely used as a fire retardant and plasticizer, has been commonly found in the environment. Its potential health-related risks, especially reproductive toxicity, have aroused concern. However, the potential cellular mechanisms remain unexplored. In this study, we aimed to investigate the molecular mechanisms underlying TEHP-caused cell damage in Sertoli cells, which play a crucial role in supporting spermatogenesis. Our findings indicate that TEHP induces apoptosis in 15P-1 mouse Sertoli cells. Subsequently, we conducted RNA sequencing analyses, which suggested that ER stress, autophagy, and MAPK-related pathways may participate in TEHP-induced cytotoxicity. Furthermore, we demonstrated that TEHP triggers ER stress, activates p38 MAPK, and inhibits autophagy flux. Then, we showed that the inhibition of ER stress or p38 MAPK activation attenuates TEHP-induced apoptosis, while the inhibition of autophagy flux is responsible for TEHP-induced apoptosis. These results collectively reveal that TEHP induces ER stress, activates p38, and inhibits autophagy flux, ultimately leading to apoptosis in Sertoli cells. These shed light on the molecular mechanisms underlying TEHP-associated testicular toxicity.

Keywords: Autophagy dysregulation; Endoplasmic reticulum stress; Reproductive toxicity; Sertoli cell; Tri (2-ethylhexyl) phosphate.

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Autophagy* / drug effects
  • Diethylhexyl Phthalate / analogs & derivatives
  • Diethylhexyl Phthalate / toxicity
  • Endoplasmic Reticulum Stress* / drug effects
  • Flame Retardants / toxicity
  • Male
  • Mice
  • Plasticizers / toxicity
  • Sequence Analysis, RNA
  • Sertoli Cells* / drug effects
  • Sertoli Cells* / metabolism
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • p38 Mitogen-Activated Protein Kinases
  • Flame Retardants
  • Plasticizers
  • Diethylhexyl Phthalate