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Medientyp:
E-Artikel
Titel:
EGFR inhibits TNF-α-mediated pathway by phosphorylating TNFR1 at tyrosine 360 and 401
Beteiligte:
Nam, Young Woo;
Shin, June-Ha;
Kim, Seongmi;
Hwang, Chi Hyun;
Lee, Choong-Sil;
Hwang, Gyuho;
Kim, Hwa-Ryeon;
Roe, Jae-Seok;
Song, Jaewhan
Erschienen:
Springer Science and Business Media LLC, 2024
Erschienen in:
Cell Death & Differentiation, 31 (2024) 10, Seite 1318-1332
Sprache:
Englisch
DOI:
10.1038/s41418-024-01316-3
ISSN:
1350-9047;
1476-5403
Entstehung:
Anmerkungen:
Beschreibung:
AbstractTumour necrosis factor receptor 1 (TNFR1) induces the nuclear factor kappa-B (NF-κB) signalling pathway and regulated cell death processes when TNF-α ligates with it. Although mechanisms regulating the downstream pathways of TNFR1 have been elucidated, the direct regulation of TNFR1 itself is not well known. In this study, we showed that the kinase domain of the epidermal growth factor receptor (EGFR) regulates NF-κB signalling and TNF-α-induced cell death by directly phosphorylating TNFR1 at Tyr 360 and 401 in its death domain. In contrast, EGFR inhibition by EGFR inhibitors, such as erlotinib and gefitinib, prevented their interaction. Once TNFR1 is phosphorylated, its death domain induces the suppression of the NF-κB pathways, complex II-mediated apoptosis, or necrosome-dependent necroptosis. Physiologically, in mouse models, EGF treatment mitigates TNF-α-dependent necroptotic skin inflammation induced by treatment with IAP and caspase inhibitors. Our study revealed a novel role for EGFR in directly regulating TNF-α-related pathways.