Sarkar Souvik, Siddiqui Asim A, Mazumder Somnath, De Rudranil, Saha Shubhra J, Banerjee Chinmoy, Iqbal Mohd S, Adhikari Susanta, Alam Athar, Roy Siddhartha, Bandyopadhyay Uday
†Division of Infectious Diseases and Immunology, CSIR-Indian Institute of Chemical Biology, 4, Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, West Bengal, India.
‡Department of Chemistry, University of Calcutta, 92, A. P. C. Road, Kolkata 700 009, West Bengal, India.
J Agric Food Chem. 2015 May 27;63(20):4988-98. doi: 10.1021/acs.jafc.5b00921. Epub 2015 May 15.
Ellagic acid (EA), a phenolic lactone, inhibited tautomerase activity of human macrophage migration inhibitory factor (MIF) noncompetitively (Ki = 1.97 ± 0.7 μM). The binding of EA to MIF was determined by following the quenching of tryptophan fluorescence. We synthesized several EA derivatives, and their structure-activity relationship studies indicated that the planar conjugated lactone moiety of EA was essential for MIF inhibition. MIF induces nuclear translocation of NF-κB and chemotaxis of peripheral blood mononuclear cells (PBMCs) to promote inflammation. We were interested in evaluating the effect of EA on nuclear translocation of NF-κB and chemotactic activity in human PBMCs in the presence of MIF. The results showed that EA inhibited MIF-induced NF-κB nuclear translocation in PBMCs, as evident from confocal immunofluorescence microscopic data. EA also inhibited MIF-mediated chemotaxis of PBMCs. Thus, we report MIF-inhibitory activity of EA and inhibition of MIF-mediated proinflammatory responses in PBMCs by EA.
鞣花酸(EA)是一种酚内酯,它以非竞争性方式抑制人巨噬细胞移动抑制因子(MIF)的互变异构酶活性(Ki = 1.97 ± 0.7 μM)。通过追踪色氨酸荧光的淬灭来确定EA与MIF的结合。我们合成了几种EA衍生物,它们的构效关系研究表明,EA的平面共轭内酯部分对于抑制MIF至关重要。MIF诱导NF-κB的核转位以及外周血单核细胞(PBMC)的趋化作用以促进炎症。我们有兴趣评估在存在MIF的情况下EA对人PBMC中NF-κB核转位和趋化活性的影响。结果表明,从共聚焦免疫荧光显微镜数据可以明显看出,EA抑制了PBMC中MIF诱导的NF-κB核转位。EA还抑制了MIF介导的PBMC趋化作用。因此,我们报道了EA对MIF的抑制活性以及EA对PBMC中MIF介导的促炎反应的抑制作用。