1. Academic Validation
  2. PM2.5 exposure induces reproductive injury through IRE1/JNK/autophagy signaling in male rats

PM2.5 exposure induces reproductive injury through IRE1/JNK/autophagy signaling in male rats

  • Ecotoxicol Environ Saf. 2021 Mar 15;211:111924. doi: 10.1016/j.ecoenv.2021.111924.
Yang Yang 1 Yajing Feng 2 Hui Huang 2 Liuxin Cui 2 Fuqin Li 3
Affiliations

Affiliations

  • 1 Department of Nosocomial Infection Management, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China. Electronic address: [email protected].
  • 2 Department of Environmental Health, College of Public Health, Zhengzhou University, Zhengzhou 450001, China.
  • 3 Department of Nosocomial Infection Management, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Abstract

Fine particulate matter (PM2.5) constitutes the most significant air pollutant that causes health risks. However, the mechanism(s) underlying PM2.5-induced male reproductive injury has not been clarified. In the present study we explored whether PM2.5 activated the inositol-requiring Enzyme 1 (IRE1)/c-Jun NH 2-terminal kinase (JNK)/autophagy-signaling pathway, and whether this pathway mediated reproductive injury in male rats. We established a male Sprague-Dawley rat model of PM2.5 (1.5 mg/kg) exposure-induced reproductive injury, and observed the intervention effects of STF083010 (an IRE1 Inhibitor, 1 mg/kg). After 4 weeks of exposure, reproductive injury-related indicators and IRE1-cascade protein expression were analyzed. Our results showed that sperm quality and serum testosterone level significantly decreased and apoptotic index increased after exposure to PM2.5. After STF083010 intervention, sperm quality and serum testosterone level were significantly improved, while the apoptotic index was reduced. Under LIGHT microscopy, we observed that the structure of spermatogenic cells in the PM2.5 group was loose, and that the numbers of spermatogenic cells and mature spermatozoa were reduced. After STF083010 intervention, the structural damage to spermatogenic cells was improved, and the number of cells shed was reduced. Western blotting analysis showed that the expression of IRE1, phosphorylated JNK (p-JNK), beclin-1, and microtubule-associated protein 1 LIGHT chain 3(LC3)II/LC3I proteins was significantly upregulated, and that the expression of p62 protein was significantly downregulated in the PM2.5 group. The concomitant administration of STF083010 significantly antagonized the aforementioned adverse effects. STF083010 exerted specific protective effects on reproductive injury-related effects in male rats exposed to PM2.5, with effects mediated via IRE1/JNK/Autophagy signaling.

Keywords

Autophagy; C-Jun NH 2-terminal kinase; Fine particulate matter; Inositol-requiring enzyme 1; Reproductive injury.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-15845
    ≥98.0%, IRE1 Inhibitor