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二酰基甘油激酶亚型特异性激活剂和抑制剂的筛选。

Screening of subtype-specific activators and inhibitors for diacylglycerol kinase.

机构信息

Department of Applied Chemistry in Bioscience, Graduate School of Agricultural Science, Faculty of Agriculture, Kobe University, Rokkodai-cho 1-1, Nada-ku, Kobe, Japan.

Department of Chemistry, Graduate School of Science, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba, Japan.

出版信息

J Biochem. 2019 Jun 1;165(6):517-522. doi: 10.1093/jb/mvz008.

Abstract

Diacylglycerol kinase (DGK) is a lipid kinase that converts diacylglycerol (DG) into phosphatidic acid (PA). DG and PA function as lipid messengers contributing to various signalling pathways. Thus, DGK plays a pivotal role in the signalling pathways by maintaining DG and PA levels. For example, DGKδ is involved in diabetes and DGKβ is important for higher brain function including memory and emotion. Recently, we also revealed that the activation of DGKα ameliorated diabetic nephropathy (DN) in mice, suggesting that DGK can be therapeutic target. However, there is no commercially available DGK subtype-specific inhibitors or activators. Therefore, in a series of experiment to find DGK subtype-specific inhibitors or activators, we tried to screen novel DGKα activators from 9,600 randomly selected compounds by using high-throughput screening we had recently developed. Finally, we obtained two lead compounds for DGKα activators, KU-8 and KU-10. Focusing KU-8, we assessed the effect of KU-8 on all mammalian DGKs activities. Thus, KU-8 activates not only DGKα but also DGKθ by approximately 20%, and strongly inhibited DGKκ. In conclusion, KU-8 would be a good lead compound for DGKα and DGKθ activators, and useful as a DGKκ inhibitor.

摘要

二酰基甘油激酶(DGK)是一种脂质激酶,可将二酰基甘油(DG)转化为磷酸脂酰基酸(PA)。DG 和 PA 作为脂质信使发挥作用,参与各种信号通路。因此,DGK 通过维持 DG 和 PA 水平在信号通路中发挥关键作用。例如,DGKδ 参与糖尿病,DGKβ 对包括记忆和情绪在内的高级大脑功能很重要。最近,我们还发现 DGKα 的激活可改善小鼠的糖尿病肾病(DN),表明 DGK 可以作为治疗靶点。然而,目前尚无商业上可用的 DGK 亚型特异性抑制剂或激活剂。因此,在一系列寻找 DGK 亚型特异性抑制剂或激活剂的实验中,我们尝试通过最近开发的高通量筛选,从 9600 种随机选择的化合物中筛选新型 DGKα 激活剂。最终,我们获得了两种 DGKα 激活剂的先导化合物,KU-8 和 KU-10。聚焦 KU-8,我们评估了 KU-8 对所有哺乳动物 DGKs 活性的影响。因此,KU-8 不仅可激活 DGKα,还可激活 DGKθ,约 20%,并强烈抑制 DGKκ。总之,KU-8 将成为 DGKα 和 DGKθ 激活剂的良好先导化合物,并可用作 DGKκ 抑制剂。

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