1. 17β-estradiol inhibits Notch1 activation in murine macrophage cell line RAW 264.7.
- Author
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Severi P, Ascierto A, Marracino L, Ouambo Talla AW, Aquila G, Martino V, Dalessandro F, Scarpante I, Minghini G, Haffreingue L, Vieceli Dalla Sega F, Fortini F, and Rizzo P
- Subjects
- Mice, Animals, RAW 264.7 Cells, Signal Transduction drug effects, Toll-Like Receptor 4 metabolism, Phosphorylation drug effects, Dipeptides pharmacology, Receptor, Notch1 metabolism, Receptor, Notch1 genetics, Estradiol pharmacology, Macrophages metabolism, Macrophages drug effects, Lipopolysaccharides pharmacology, Interferon-gamma metabolism
- 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., (© 2024. The Author(s), under exclusive licence to Springer Nature B.V.)
- Published
- 2024
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