Quinoline-Pyrazole Scaffold as a Novel Ligand of Galectin-3 and Suppressor of TREM2 Signaling

被引:18
作者
Gabr, Moustafa [3 ]
Rehman, Ashfaq Ur [1 ,2 ]
Chen, Hai-Feng [2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med SJTU SM, Med Bioinformat Ctr, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, State Key Lab Microbial Metab, Natl Expt Teaching Ctr Life Sci & Biotechnol, Dept Bioinformat & Biostat,Coll Life Sci & Biotec, Shanghai 200240, Peoples R China
[3] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
关键词
Galectin-3; neurological disorders; FRET assay; neuroinflammation; Alzheimer's disease; ALZHEIMERS-DISEASE; HEART-FAILURE; MICROGLIA; AFFINITY; DERIVATIVES; INHIBITION; ACTIVATION; ARGININE; UPDATE; TARGET;
D O I
10.1021/acsmedchemlett.0c00330
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Galectin-3 has been identified as a critical player in driving the neuroinflammatory responses in Alzheimer's disease (AD). A key feature of this function of galectin-3 is associated with its interaction with the triggering receptor expressed on myeloid cells-2 (TREM2). Herein, we report a high-throughput screening (HTS) platform that can be used for the identification of inhibitors of TREM2 and galectin-3 interaction. We have utilized this HTS assay to screen a focused library of compounds optimized for the central nervous system (CNS)-related diseases. MG-257 was identified from this screen as the first example of a small molecule that can attenuate TREM2 signaling based on its high affinity to galectin-3 (endogenous ligand of TREM2). Remarkably, MG-257 reduced the levels of proinflammatory cytokines in activated microglial cells, which highlights its ability to inhibit the neuroinflammatory response associated with AD.
引用
收藏
页码:1759 / 1765
页数:7
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