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

机译:喹啉 - 吡唑脚手架作为Galectin-3的新型配体和Trem2信号传导的抑制剂

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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.
机译:Galectin-3已被识别为在阿尔茨海默病(AD)中驱动神经炎炎症反应的关键球员。 Galectin-3的这种功能的关键特征与其与髓样细胞-2(Trem2)的触发受体的相互作用有关。 在此,我们报告了一种高通量筛选(HTS)平台,可用于鉴定Trem2和Galectin-3相互作用的抑制剂。 我们利用这种HTS测定来筛选针对中枢神经系统(CNS)相关疾病优化的聚焦文库。 将Mg-257从该屏幕中鉴定为可以基于其对Galectin-3(Trem2的内源性配体)的高亲和力来衰减Trem2信号传导的小分子的第一实例。 值得注意的是,MG-257减少了活性的小胶质细胞中促炎细胞因子的水平,其突出了其抑制与广告相关的神经炎性反应的能力。

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