Reactive oxygen species (ROS) production triggered by prostaglandin D2 (PGD2) regulates lactate dehydrogenase (LDH) expression/activity in TM4 Sertoli cells

Mol Cell Endocrinol. 2016 Oct 15:434:154-65. doi: 10.1016/j.mce.2016.06.021. Epub 2016 Jun 18.

Abstract

Reactive oxygen species (ROS) regulate testicular function in health and disease. We previously described a prostaglandin D2 (PGD2) system in Sertoli cells. Now, we found that PGD2 increases ROS and hydrogen peroxide (H2O2) generation in murine TM4 Sertoli cells, and also induces antioxidant enzymes expression suggesting that defense systems are triggered as an adaptive stress mechanism that guarantees cell survival. ROS and specially H2O2 may act as second messengers regulating signal transduction pathways and gene expression. We describe a stimulatory effect of PGD2 on lactate dehydrogenase (LDH) expression via DP1/DP2 receptors, which is prevented by the antioxidant N-acetyl-L-cysteine and the PI3K/Akt pathway inhibitor LY 294002. PGD2 also enhances Akt and CREB/ATF-1 phosphorylation. Our results provide evidence for a role of PGD2 in the regulation of the oxidant/antioxidant status in Sertoli cells and, more importantly, in the modulation of LDH expression which takes place through ROS generation and the Akt-CREB/ATF-1 pathway.

Keywords: H(2)O(2); Lactate dehydrogenase; Prostaglandin D(2); Reactive oxygen species; Sertoli cell; Testis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Cell Line
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation / drug effects
  • Humans
  • Hydrogen Peroxide / metabolism
  • Lactate Dehydrogenases / metabolism*
  • Male
  • Mice
  • Prostaglandin D2 / pharmacology*
  • Reactive Oxygen Species / metabolism*
  • Sertoli Cells / drug effects
  • Sertoli Cells / metabolism*
  • Signal Transduction / drug effects
  • Transcription Factor DP1 / genetics
  • Transcription Factor DP1 / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • DNA-Binding Proteins
  • Reactive Oxygen Species
  • TFDP1 protein, human
  • TFDP2 protein, human
  • Transcription Factor DP1
  • Transcription Factors
  • Hydrogen Peroxide
  • Lactate Dehydrogenases
  • Prostaglandin D2