首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >15-Deoxy-Delta (12,14)-PGJ2 inhibits astrocyte IL-1 signaling: inhibition of NF-kappaB and MAP kinase pathways and suppression of cytokine and chemokine expression.
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15-Deoxy-Delta (12,14)-PGJ2 inhibits astrocyte IL-1 signaling: inhibition of NF-kappaB and MAP kinase pathways and suppression of cytokine and chemokine expression.

机译:15-脱氧-三角洲(12,14)-PGJ2抑制星形胶质细胞IL-1信号传导:抑制NF-κB和MAP激酶途径,并抑制细胞因子和趋化因子的表达。

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摘要

We studied the role of 15-deoxy-Delta (12,14)-PGJ2 (15d-PGJ2), a macrophage inhibitor with reported therapeutic effects on experimental allergic encephalomyelitis, in human astrocyte activation in vitro. 15d-PGJ2 inhibited a broad range of astrocyte inflammatory gene expression induced by IL-1, including cytokines (TNFalpha and IL-6), chemokines (RANTES/CCL5 and IP-10/CXCL10) and inducible nitric oxide synthase. 15d-PGJ2 inhibited transactivation of NF-kappaB-dependent promoters, as well as p38 and JNK MAPK phosphorylation induced by IL-1, while having no inhibitory effect on IFN-induced Stat signaling pathways. Our results demonstrating 15d-PGJ2-mediated astrocyte deactivation through inhibition of NF-kappaB are similar to those described for macrophages, and add astrocytes as additional targets for this prostaglandin (PG).
机译:我们研究了15-脱氧-三角洲(12,14)-PGJ2(15d-PGJ2)的作用,在人类星形胶质细胞体外激活中,巨噬细胞抑制剂对实验性变应性脑脊髓炎具有治疗作用。 15d-PGJ2抑制由IL-1诱导的多种星形胶质细胞炎症基因表达,包括细胞因子(TNFα和IL-6),趋化因子(RANTES / CCL5和IP-10 / CXCL10)和诱导型一氧化氮合酶。 15d-PGJ2抑制NF-κB依赖性启动子的反式激活,以及IL-1诱导的p38和JNK MAPK磷酸化,而对IFN诱导的Stat信号通路没有抑制作用。我们的研究结果表明,通过抑制NF-κB介导的15d-PGJ2介导的星形胶质细胞失活与针对巨噬细胞描述的结果相似,并添加了星形胶质细胞作为该前列腺素(PG)的其他靶标。

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