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TNF-α 通过 TRAF2-GRK2 复合物的关联损害原代成纤维样滑膜细胞中的 EP4 信号。

TNF-α impairs EP4 signaling through the association of TRAF2-GRK2 in primary fibroblast-like synoviocytes.

机构信息

Institute of Clinical Pharmacology, Anhui Medical University, Key Laboratory of Anti-inflammatory and Immune Medicine (Anhui Medical University), Ministry of Education, Hefei, 230032, China.

Department of Pharmacy, Maanshan Hospital of Traditional Chinese Medicine, Maanshan, 243000, China.

出版信息

Acta Pharmacol Sin. 2022 Feb;43(2):401-416. doi: 10.1038/s41401-021-00654-z. Epub 2021 Apr 15.

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.

摘要

我们之前的研究表明,肿瘤坏死因子-α(TNF-α)的慢性治疗会降低胶原诱导关节炎(CIA)大鼠成纤维样滑膜细胞(FLS)中的 cAMP 浓度。在这项研究中,我们研究了 TNF-α如何损害 cAMP 动态平衡,特别是阐明 TNF-α和前列腺素受体 4(EP4)信号的潜在下游分子,这些分子可能相互作用。使用 cAMP FRET 生物传感器 PM-ICUE3,我们证明 TNF-α(20ng/mL)阻断了 ONO-4819 触发的 EP4 信号,但不阻断 Butaprost 触发的 EP2 信号在正常大鼠 FLS 中。我们表明,TNF-α(0.02-20ng/mL)剂量依赖性地降低了正常大鼠 FLS 中 EP4 的膜分布。TNF-α通过募集肿瘤坏死因子受体相关因子 2(TRAF2)到细胞膜显著增加人成纤维样滑膜细胞(hFLS)中的 TNF 受体 2(TNFR2)表达并刺激增殖。更有趣的是,我们揭示了 TRAF2 在原代 hFLS 的细胞质中与 G 蛋白偶联受体激酶(GRK2)相互作用,并在 TNF-α刺激时帮助将 GRK2 带到细胞膜上,TRAF2 和 GRK2 的复合物在膜上分离,然后转位 GRK2 诱导 EP4 的脱敏和内化,导致细胞内 cAMP 产生减少。siRNA 沉默 TRAF2 显著减少了 TRAF2-GRK2 相互作用,阻断了 GRK2 的易位,并导致膜上 EP4 和细胞内 cAMP 的表达上调。在 CIA 大鼠中,给予帕罗西汀抑制 GRK2 可有效改善症状和临床参数,显著减少关节滑膜炎症和骨破坏。这些结果阐明了 TNFR(细胞因子受体)和 EP4(典型的 G 蛋白偶联受体)信号通路之间的一种新的串扰形式。TRAF2 和 GRK2 之间的相互作用可能成为治疗炎症性疾病的潜在新药物靶点。

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Structure of TRAF Family: Current Understanding of Receptor Recognition.TRAF 家族结构:受体识别的最新认识。
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