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- W3153597514 abstract "Our previous study showed that chronic treatment with tumor necrosis factor-α (TNF-α) decreased cAMP concentration in fibroblast-like synoviocytes (FLSs) of collagen-induced arthritis (CIA) rats. In this study we investigated how TNF-α impairs cAMP homeostasis, particularly clarifying the potential downstream molecules of TNF-α and prostaglandin receptor 4 (EP4) signaling that would interact with each other. Using a cAMP FRET biosensor PM-ICUE3, we demonstrated that TNF-α (20 ng/mL) blocked ONO-4819-triggered EP4 signaling, but not Butaprost-triggered EP2 signaling in normal rat FLSs. We showed that TNF-α (0.02–20 ng/mL) dose-dependently reduced EP4 membrane distribution in normal rat FLS. TNF-α significantly increased TNF receptor 2 (TNFR2) expression and stimulated proliferation in human FLS (hFLS) via ecruiting TNF receptor-associated factor 2 (TRAF2) to cell membrane. More interestingly, we revealed that TRAF2 interacted with G protein-coupled receptor kinase (GRK2) in the cytoplasm of primary hFLS and helped to bring GRK2 to cell membrane in response of TNF-α stimulation, the complex of TRAF2 and GRK2 then separated on the membrane, and translocated GRK2 induced the desensitization and internalization of EP4, leading to reduced production of intracellular cAMP. Silencing of TRAF2 by siRNA substantially diminished TRAF2-GRK2 interaction, blocked the translocation of GRK2, and resulted in upregulated expression of membrane EP4 and intracellular cAMP. In CIA rats, administration of paroxetine to inhibit GRK2 effectively improved the symptoms and clinic parameters with significantly reduced joint synovium inflammation and bone destruction. These results elucidate a novel form of cross-talk between TNFR (a cytokine receptor) and EP4 (a typical G protein-coupled receptor) signaling pathways. The interaction between TRAF2 and GRK2 may become a potential new drug target for the treatment of inflammatory diseases." @default.
- W3153597514 created "2021-04-26" @default.
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- W3153597514 date "2021-04-15" @default.
- W3153597514 modified "2023-10-14" @default.
- W3153597514 title "TNF-α impairs EP4 signaling through the association of TRAF2-GRK2 in primary fibroblast-like synoviocytes" @default.
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- W3153597514 cites W1974629810 @default.
- W3153597514 cites W1976645168 @default.
- W3153597514 cites W1985345244 @default.
- W3153597514 cites W1989707466 @default.
- W3153597514 cites W1998364728 @default.
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- W3153597514 cites W2000468514 @default.
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- W3153597514 cites W2018745984 @default.
- W3153597514 cites W2023694551 @default.
- W3153597514 cites W2026679068 @default.
- W3153597514 cites W2027239096 @default.
- W3153597514 cites W2027857069 @default.
- W3153597514 cites W2031716499 @default.
- W3153597514 cites W2035242925 @default.
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- W3153597514 cites W2042161082 @default.
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- W3153597514 cites W2056754627 @default.
- W3153597514 cites W2059000751 @default.
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- W3153597514 cites W2061946742 @default.
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- W3153597514 doi "https://doi.org/10.1038/s41401-021-00654-z" @default.
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