Resatorvid (TAK-242)通过TLR4/JAK2/STAT3信号通路调节巨噬细胞极化和T辅助细胞平衡,从而改善溃疡性结肠炎。

IF 4.5 2区 医学 Q2 CELL BIOLOGY Inflammation Pub Date : 2024-12-01 Epub Date: 2024-05-18 DOI:10.1007/s10753-024-02028-z
Xiaoling Huang, Rong Lin, Huan Liu, Mengying Dai, Jiejie Guo, Wenjia Hui, Weidong Liu, Milamuguli Haerken, Ruixue Zheng, Tangnuer Yushanjiang, Feng Gao
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引用次数: 0

摘要

Resatorvid(TAK-242)是Toll样受体-4(TLR4)的特异性抑制剂,因其抗炎特性而备受关注。尽管如此,很少有研究评估其对溃疡性结肠炎(UC)的影响。本研究旨在探讨TAK-242对巨噬细胞极化和T辅助细胞平衡的影响及其缓解UC的机制。我们的研究结果表明,在UC患者、UC小鼠模型和发生炎症反应的HT29细胞中,TLR4表达升高。TAK-242治疗可减少TNF-α和LPS刺激下HT29细胞的凋亡,缓解右旋糖酐硫酸钠(DSS)诱导的体内结肠炎症状。TAK-242 下调了 TLR4 的表达,减少了促炎细胞因子 TNF-α、IL-6 和 IL-1β 的分泌,同时提高了 IL-10 的分泌。TAK-242 还能降低 M1 巨噬细胞的极化,减少 Th1 和 Th17 细胞的浸润,同时增加 Th2 细胞的浸润和 M2 巨噬细胞的极化。从机理上讲,TAK-242抑制了巨噬细胞极化和T辅助细胞平衡的重要调节因子JAK2/STAT3信号通路。此外,服用JAK2/STAT3拮抗剂AG490可部分抵消TAK-242在体内和体外的作用,这表明TAK-242是通过抑制JAK2/STAT3通路来发挥其生物活性的。综上所述,这项研究强调了TAK-242是一种很有前景的抗UC药物,它通过TLR4/JAK2/STAT3信号通路调节巨噬细胞极化和T辅助细胞平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Resatorvid (TAK-242) Ameliorates Ulcerative Colitis by Modulating Macrophage Polarization and T Helper Cell Balance via TLR4/JAK2/STAT3 Signaling Pathway.

Resatorvid (TAK-242), a specific inhibitor of Toll-like receptor-4 (TLR4), has attracted attention for its anti-inflammatory properties. Despite this, few studies have evaluated its effects on ulcerative colitis (UC). This study aimed to investigate the effects of TAK-242 on macrophage polarization and T helper cell balance and the mechanism by which it alleviates UC. Our findings indicated that TLR4 expression was elevated in patients with UC, a mouse model of UC, and HT29 cells undergoing an inflammatory response. TAK‑242 treatment reduced apoptosis in TNF-α and LPS-stimulated HT29 cells and alleviated symptoms of dextran sulfate sodium (DSS)‑induced colitis in vivo. TAK‑242 downregulated TLR4 expression and decreased the secretion of pro-inflammatory cytokines TNF-α, IL-6, and IL-1β while enhancing IL-10 production. TAK-242 also reduced M1 macrophage polarization and diminished Th1 and Th17 cell infiltration while increasing Th2 cell infiltration and M2 macrophage polarization both in vitro and in vivo. Mechanistically, TAK-242 inhibited the JAK2/STAT3 signaling pathway, an important regulator of macrophage polarization and T helper cell balance. Furthermore, the in vivo and in vitro effects of TAK-242 were partially negated by the administration of the JAK2/STAT3 antagonist AG490, suggesting that TAK-242 inhibits the JAK2/STAT3 pathway to exert its biological activities. Taken together, this study underscores TAK-242 as a promising anti-UC agent, functioning by modulating macrophage polarization and T helper cell balance via the TLR4/JAK2/STAT3 signaling pathway.

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来源期刊
Inflammation
Inflammation 医学-免疫学
CiteScore
9.70
自引率
0.00%
发文量
168
审稿时长
3.0 months
期刊介绍: Inflammation publishes the latest international advances in experimental and clinical research on the physiology, biochemistry, cell biology, and pharmacology of inflammation. Contributions include full-length scientific reports, short definitive articles, and papers from meetings and symposia proceedings. The journal''s coverage includes acute and chronic inflammation; mediators of inflammation; mechanisms of tissue injury and cytotoxicity; pharmacology of inflammation; and clinical studies of inflammation and its modification.
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