17β-estradiol inhibits Notch1 activation in murine macrophage cell line RAW 264.7

Mol Biol Rep. 2024 Nov 8;51(1):1134. doi: 10.1007/s11033-024-10058-x.

Abstract

Background: Macrophages are major effectors in regulating immune response and inflammation. The pro-inflammatory phenotype (M1) is induced by the activation of the Toll-like receptor 4 (TLR4) on the macrophage surface, which recognizes lipopolysaccharide (LPS), a component of Gram-negative bacterial wall, and by the binding of interferon-gamma (IFNγ), a cytokine released by activated T lymphocytes, to its receptor (IFNGR). Among the pathways activated by LPS/IFNγ is the Notch pathway, which promotes the M1 phenotype. Conversely, 17β-estradiol (E2) has been shown to blunt LPS-mediated inflammatory response. While it has been shown that E2 regulates the activity of the Notch1 receptor in human endothelial cells, there is no evidence of estrogen-mediated regulation of Notch1 in macrophages.

Methods and results: In this study, RAW 264.7 cells were stimulated with LPS/IFNγ in the presence or absence of E2 and/or N-[N-(3,5-difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl ester (DAPT), an inhibitor of γ-secretase, the enzyme involved in Notch activation. The effects of treatment on inducible nitric oxide synthase (iNOS), on components of the Notch pathway, and MAPK (mitogen-activated protein kinase) were assessed by quantitative PCR and Western blotting. We found that E2, through a mechanism involving the inhibition of p38 phosphorylation, reduces the activation of Notch1 induced by LPS/IFNγ. On the contrary, Notch1 exerts a negative control on the estrogen receptor α (ERα) since Notch1 inhibition increases the protein levels of this receptor.

Conclusion: In conclusion, we report for the first time a Notch-ERα interaction in macrophages. Our data suggest that E2 may reduce LPS/IFNγ-mediated M1 pro-inflammatory phenotype in macrophages by inhibiting Notch1. This finding encourages further studies on Notch1 inhibitors as novel treatments for inflammation-related diseases.

Keywords: 17β-estradiol; Inflammation; Macrophages; Notch pathway.

MeSH terms

  • Animals
  • Dipeptides / pharmacology
  • Estradiol* / pharmacology
  • Interferon-gamma* / metabolism
  • Lipopolysaccharides* / pharmacology
  • Macrophages* / drug effects
  • Macrophages* / metabolism
  • Mice
  • Phosphorylation / drug effects
  • RAW 264.7 Cells
  • Receptor, Notch1* / genetics
  • Receptor, Notch1* / metabolism
  • Signal Transduction / drug effects
  • Toll-Like Receptor 4 / metabolism

Substances

  • Receptor, Notch1
  • Estradiol
  • Lipopolysaccharides
  • Interferon-gamma
  • Notch1 protein, mouse
  • Toll-Like Receptor 4
  • Dipeptides