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新型合成葡二糖 RSCL-0409——一种脂多糖诱导的 Toll 样受体介导信号通路拮抗剂。

Novel synthetic gluco-disaccharide RSCL-0409--a lipopolysaccharide-induced Toll-like receptor-mediated signalling antagonist.

机构信息

Drug Discovery and Development Group, Reliance Life Sciences Pvt. Ltd, Navi Mumbai, India.

出版信息

FEBS J. 2010 Apr;277(7):1639-52. doi: 10.1111/j.1742-4658.2010.07589.x. Epub 2010 Feb 17.

Abstract

The regulation of cytokines and pro-inflammatory genes is an absolute essentiality to combat inflammatory diseases. The present study investigated the effects of 4-O-chloroacetyl-2,3-di-O-acetyl-6-O-levulinoyl-beta-d-glucopyranosyl]-(1-3)-1-O-(p-methoxyphenyl)-2-deoxy-2-N-trichloroacetyl-4,6-O-benzylidene-alpha-d-glucopyranoside (RSCL-0409), a novel small molecule Toll-like receptor (TLR) signalling antagonist, and its mechanism of action in human monocytic (THP-1) cells stimulated with lipopolysaccharide (LPS). In THP-1 and RAW264.7 cells, RSCL-0409 suppressed LPS-induced production of tumour necrosis factor-alpha (TNF-alpha) with a 50% inhibitory concentration of 10.6 mum and mRNA expression of ICAM-1, Cox-2 and interleukin-8 with no evidence of cytotoxicity. RSCL-0409 also suppressed TNF-alpha production from LPS-stimulated human peripheral blood mononuclear cells. Similar results were obtained in vivo in a murine model of LPS-induced inflammation, where pretreatment with RSCL-0409 resulted in significant inhibition of TNF-alpha. It is also noteworthy that RSCL-0409 suppressed the cytokine production induced by TLR2 and -4 ligands and not for any other TLR ligands. RSCL-0409 significantly inhibited p65 nuclear translocation induced by LPS. In conclusion, RSCL-0409, a novel small molecule, is the first of its kind in the category of carbohydrate-derived TLR signalling antagonists and could definitely be a promising therapeutic agent for inflammatory diseases whose pathogenesis involves TLR2- or TLR4-mediated signalling processes.

摘要

细胞因子和促炎基因的调节对于治疗炎症性疾病是绝对必要的。本研究探讨了新型小分子 Toll 样受体(TLR)信号转导拮抗剂 4-O-氯乙酰基-2,3-二-O-乙酰基-6-O-乙酰基-β-D-吡喃葡萄糖基]-(1-3)-1-O-(对甲氧基苯基)-2-去氧-2-N-三氯乙酰基-4,6-O-苄叉-α-D-吡喃葡萄糖苷(RSCL-0409)及其作用机制在脂多糖(LPS)刺激的人单核细胞(THP-1)细胞中的作用。在 THP-1 和 RAW264.7 细胞中,RSCL-0409 抑制 LPS 诱导的肿瘤坏死因子-α(TNF-α)的产生,其 50%抑制浓度为 10.6 µm,ICAM-1、Cox-2 和白细胞介素-8 的 mRNA 表达也没有证据表明细胞毒性。RSCL-0409 还抑制了 LPS 刺激的人外周血单核细胞中 TNF-α的产生。在 LPS 诱导的炎症的小鼠模型中,体内也获得了类似的结果,其中 RSCL-0409 的预处理导致 TNF-α的显著抑制。值得注意的是,RSCL-0409 抑制了 TLR2 和 TLR4 配体诱导的细胞因子产生,而不是其他任何 TLR 配体。RSCL-0409 显著抑制了 LPS 诱导的 p65 核易位。总之,RSCL-0409 是一种新型小分子,是碳水化合物衍生的 TLR 信号转导拮抗剂中的首例,对于涉及 TLR2 或 TLR4 介导的信号转导过程的炎症性疾病,它肯定是一种有前途的治疗药物。

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