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

被引:10
作者
Kalluri, Mani D. [1 ]
Datla, Praneel [2 ]
Bellary, Akshaya [1 ]
Basha, Khalander [1 ]
Sharma, Ashwani [1 ]
Sharma, Anuradha [1 ]
Singh, Shiva [1 ]
Upadhyay, Shakti [2 ]
Rajagopal, Vikram [1 ]
机构
[1] Reliance Life Sci Pvt Ltd, Drug Discovery & Dev Grp, Dhirubhai Ambani Life Sci Ctr, Navi Mumbai 400701, India
[2] EID Parry India Ltd, Chennai, Tamil Nadu, India
关键词
inflammation; lipopolysaccharide; monocytes; NF-kappa B; TLR signalling; tumour necrosis factor-alpha; NF-KAPPA-B; ENDOTOXIN ANTAGONIST; GENE-EXPRESSION; IN-VIVO; INNATE; RECOGNITION; TLR4; LPS; INHIBITION; ACTIVATION;
D O I
10.1111/j.1742-4658.2010.07589.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mu m 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.
引用
收藏
页码:1639 / 1652
页数:14
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