Frontiers in Endocrinology (Oct 2024)

Activation of estrogen-related receptor γ by calcium and cadmium

  • Qiaochu Wang,
  • Nanxi Huang,
  • John B. Psaltis,
  • Reem M. Gahtani,
  • Gai Yan,
  • Dajun Lu,
  • Shannon R. Cahalan,
  • Xu Shi,
  • Robert L. Copeland,
  • Bassem R. Haddad,
  • Mary Beth Martin,
  • Mary Beth Martin

DOI
https://doi.org/10.3389/fendo.2024.1400022
Journal volume & issue
Vol. 15

Abstract

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ObjectiveEstrogen-related receptor γ (ERRγ) is a metabolic regulator with no identified physiological ligands. This study investigates whether calcium is an ERRγ ligand that mediates the effects of glucagon and whether cadmium, which mimics the effects of calcium, disrupts metabolism through ERRγ.MethodHepG2, MCF-7, and HEK293T transfected with ERRγ were treated with glucagon, calcium, cadmium, ERRγ agonist, or ERRγ inhibitor. Cells were then collected for in vitro assays including real-time qPCR, Western blot, ChIP, immunofluorescence, mutational analysis, or gene set enrichment analysis. Molecular dynamics simulations were performed to study mutation sites.ResultsIn HepG2 cells, treatment with glucagon, calcium, or cadmium re-localized ERRγ to the cell nucleus, recruited ERRγ to estrogen-related response elements, induced the expression of ERRγ-regulated genes, and increased extracellular glucose that was blocked by an ERRγ antagonist. In MCF-7 cells and HEK293T cells transfected with ERRγ, similar treatments induced the expression of metabolic genes. Mutational analysis identified S303, T429, and E452 in the ligand-binding domain as potential interaction sites. Molecular dynamics simulations showed that calcium induced changes in ERRγ similar to ERRγ agonist.ConclusionThe results suggest that calcium is a potential ligand of ERRγ that mediates the effects of glucagon and cadmium disrupts metabolism through ERRγ.

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