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ORAI钙通道:调节、功能、药理学及治疗靶点

ORAI Calcium Channels: Regulation, Function, Pharmacology, and Therapeutic Targets.

作者信息

Rubaiy Hussein N

机构信息

Department of Laboratory Medicine, Division of Clinical Pharmacology, Karolinska Institute and Karolinska University Hospital, C1:68, 141 86 Stockholm, Sweden.

出版信息

Pharmaceuticals (Basel). 2023 Jan 22;16(2):162. doi: 10.3390/ph16020162.

Abstract

The changes in intracellular free calcium (Ca) levels are one of the most widely regulators of cell function; therefore, calcium as a universal intracellular mediator is involved in very important human diseases and disorders. In many cells, Ca inflow is mediated by store-operated calcium channels, and it is recognized that the store-operated calcium entry (SOCE) is mediated by the two partners: the pore-forming proteins Orai (Orai1-3) and the calcium store sensor, stromal interaction molecule (STIM1-2). Importantly, the Orai/STIM channels are involved in crucial cell signalling processes such as growth factors, neurotransmitters, and cytokines via interaction with protein tyrosine kinase coupled receptors and G protein-coupled receptors. Therefore, in recent years, the issue of Orai/STIM channels as a drug target in human diseases has received considerable attention. This review summarizes and highlights our current knowledge of the Orai/STIM channels in human diseases and disorders, including immunodeficiency, myopathy, tubular aggregate, Stormorken syndrome, York platelet syndrome, cardiovascular and metabolic disorders, and cancers, as well as suggesting these channels as drug targets for pharmacological therapeutic intervention. Moreover, this work will also focus on the pharmacological modulators of Orai/STIM channel complexes. Together, our thoughtful of the biology and physiology of the Orai/STIM channels have grown remarkably during the past three decades, and the next important milestone in the field of store-operated calcium entry will be to identify potent and selective small molecules as a therapeutic agent with the purpose to target human diseases and disorders for patient benefit.

摘要

细胞内游离钙(Ca)水平的变化是细胞功能最广泛的调节因子之一;因此,钙作为一种普遍的细胞内介质,参与了非常重要的人类疾病和紊乱。在许多细胞中,Ca内流由储存操纵性钙通道介导,并且人们认识到储存操纵性钙内流(SOCE)由两个伙伴介导:形成孔道的蛋白Orai(Orai1 - 3)和钙储存传感器——基质相互作用分子(STIM1 - 2)。重要的是,Orai/STIM通道通过与蛋白酪氨酸激酶偶联受体和G蛋白偶联受体相互作用,参与生长因子、神经递质和细胞因子等关键细胞信号转导过程。因此,近年来,Orai/STIM通道作为人类疾病药物靶点的问题受到了相当多的关注。本综述总结并突出了我们目前对人类疾病和紊乱中Orai/STIM通道的认识,包括免疫缺陷、肌病、管状聚集物、斯托莫尔肯综合征、约克血小板综合征、心血管和代谢紊乱以及癌症,同时建议将这些通道作为药物靶点进行药理治疗干预。此外,这项工作还将聚焦于Orai/STIM通道复合物的药理调节剂。总的来说,在过去三十年里,我们对Orai/STIM通道的生物学和生理学的认识有了显著增长,储存操纵性钙内流领域的下一个重要里程碑将是确定强效且选择性的小分子作为治疗剂,以针对人类疾病和紊乱造福患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bad/9967976/289945d3fd6f/pharmaceuticals-16-00162-g001.jpg

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