The Tpl2-MEK pathway plays a critical role in spheroid-cultured endometriotic stromal cells

Am J Reprod Immunol. 2023 May;89(5):e13689. doi: 10.1111/aji.13689. Epub 2023 Feb 22.

Abstract

Problem: Endometriosis is a proliferative disease characterized by cytokine-induced inflammation. The objective of this study was to assess cell growth and PGE2 production induced by TNF-α in endometriotic stromal cells (ESCs) in spheroid cell culture and to identify the signaling pathway involved with a view to finding new therapeutic targets for endometriosis.

Method of study: Tissue samples were collected from patients with and without endometriosis. ESCs were isolated from ovarian endometrioma (OE). Gene expression was evaluated by real-time PCR and DNA microarray analysis, the proliferative effect on ESCs by WST-8 assay, and PGE2 production by ELISA. Protein phosphorylation was detected using western blotting.

Results: COX-2, aromatase and VEGFA mRNA expression and PGE2 production were significantly elevated in spheroid cell cultures compared to monolayer cell cultures. TNF-α receptor (TNFR) 1 and TNFR2 mRNA was also significantly increased. TNF-α promoted the proliferation and PGE2 production of ESCs in spheroid cell cultures significantly more than in monolayer cell cultures. TNF-α increased the expression of several genes related to the pathophysiology of endometriosis in spheroid ESCs. DNA microarray analysis revealed that the Tpl2 gene, which codes for a MAPK upstream of MEK, was upregulated in OE and endometrium with endometriosis compared to normal endometrium. TNF-α increased the phosphorylation and expression of Tpl2 and MEK, and Tpl2 and MEK inhibitors inhibited TNF-α-induced proliferation and PGE2 production in spheroid ESCs.

Conclusion: The Tpl2-MEK signaling pathway may play a critical role in the cell growth and PGE2 production induced by TNF-α in spheroid ESCs.

Keywords: TNF-α; Tpl2-MEK pathway; endometriosis; inflammation; proliferation; spheroid culture.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • DNA / metabolism
  • Dinoprostone / metabolism
  • Endometriosis* / metabolism
  • Endometrium / metabolism
  • Female
  • Humans
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mitogen-Activated Protein Kinase Kinases / pharmacology
  • Mitogen-Activated Protein Kinase Kinases / therapeutic use
  • RNA, Messenger / metabolism
  • Stromal Cells / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Dinoprostone
  • DNA
  • Mitogen-Activated Protein Kinase Kinases
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • MAP3K8 protein, human