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A new selective pharmacological enhancer of the Orai1 Ca channel reveals roles for Orai1 in smooth and skeletal muscle functions.一种新型的Orai1钙通道选择性药理学增强剂揭示了Orai1在平滑肌和骨骼肌功能中的作用。
ACS Pharmacol Transl Sci. 2020 Feb 14;3(1):135-147. doi: 10.1021/acsptsci.9b00081. Epub 2020 Jan 13.
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FASEB J. 2016 Dec;30(12):4109-4119. doi: 10.1096/fj.201600621R. Epub 2016 Sep 1.

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本文引用的文献

1
A calcium/cAMP signaling loop at the ORAI1 mouth drives channel inactivation to shape NFAT induction.钙离子/环腺苷酸信号环作用于 ORAI1 孔道以调控通道失活从而调节 NFAT 的诱导。
Nat Commun. 2019 Apr 29;10(1):1971. doi: 10.1038/s41467-019-09593-0.
2
Pyrtriazoles, a Novel Class of Store-Operated Calcium Entry Modulators: Discovery, Biological Profiling, and in Vivo Proof-of-Concept Efficacy in Acute Pancreatitis.吡咯并三嗪类化合物,新型的储存操纵钙内流调节剂:发现、生物学特征分析,以及在急性胰腺炎中的体内概念验证疗效。
J Med Chem. 2018 Nov 8;61(21):9756-9783. doi: 10.1021/acs.jmedchem.8b01512. Epub 2018 Oct 30.
3
Gain-of-function mutations in STIM1 and ORAI1 causing tubular aggregate myopathy and Stormorken syndrome.STIM1 和 ORAI1 功能获得性突变导致管状聚集性肌病和 Stormorken 综合征。
Cell Calcium. 2018 Dec;76:1-9. doi: 10.1016/j.ceca.2018.07.008. Epub 2018 Sep 3.
4
CRAC channels as targets for drug discovery and development.CRAC 通道作为药物发现和开发的靶点。
Cell Calcium. 2018 Sep;74:147-159. doi: 10.1016/j.ceca.2018.07.005. Epub 2018 Jul 18.
5
Junctional membrane Ca dynamics in human muscle fibers are altered by malignant hyperthermia causative RyR mutation.人类肌纤维连接膜钙动力学受致恶性高热的 RyR 突变改变。
Proc Natl Acad Sci U S A. 2018 Aug 7;115(32):8215-8220. doi: 10.1073/pnas.1800490115. Epub 2018 Jul 23.
6
Measurement of force and calcium release using mechanically skinned fibers from mammalian skeletal muscle.使用哺乳动物骨骼肌机械剥皮纤维测量力和钙释放。
J Appl Physiol (1985). 2018 Oct 1;125(4):1105-1127. doi: 10.1152/japplphysiol.00445.2018. Epub 2018 Jul 19.
7
An SAR study of hydroxy-trifluoromethylpyrazolines as inhibitors of Orai1-mediated store operated Ca entry in MDA-MB-231 breast cancer cells using a convenient Fluorescence Imaging Plate Reader assay.一种 SAR 研究:羟基三氟甲基吡唑啉作为 Orai1 介导的储存操纵性 Ca 内流抑制剂在 MDA-MB-231 乳腺癌细胞中的应用,采用了一种方便的荧光成像板读数测定法。
Bioorg Med Chem. 2018 Jul 23;26(12):3406-3413. doi: 10.1016/j.bmc.2018.05.012. Epub 2018 May 9.
8
The STIM-Orai Pathway: Orai, the Pore-Forming Subunit of the CRAC Channel.STIM-Orai信号通路:Orai,CRAC通道的孔形成亚基。
Adv Exp Med Biol. 2017;993:39-57. doi: 10.1007/978-3-319-57732-6_3.
9
Human skeletal muscle plasmalemma alters its structure to change its Ca-handling following heavy-load resistance exercise.大强度抗阻运动后,人骨骼肌细胞质膜改变其结构以改变其钙处理能力。
Nat Commun. 2017 Feb 13;8:14266. doi: 10.1038/ncomms14266.
10
Evaluation of known and novel inhibitors of Orai1-mediated store operated Ca entry in MDA-MB-231 breast cancer cells using a Fluorescence Imaging Plate Reader assay.使用荧光成像微孔板读数仪检测法评估MDA-MB-231乳腺癌细胞中Orai1介导的储存式钙内流的已知和新型抑制剂。
Bioorg Med Chem. 2017 Jan 1;25(1):440-449. doi: 10.1016/j.bmc.2016.11.007. Epub 2016 Nov 7.

一种新型的Orai1钙通道选择性药理学增强剂揭示了Orai1在平滑肌和骨骼肌功能中的作用。

A new selective pharmacological enhancer of the Orai1 Ca channel reveals roles for Orai1 in smooth and skeletal muscle functions.

作者信息

Azimi Iman, Stevenson Ralph J, Zhang Xuexin, Meizoso-Huesca Aldo, Xin Ping, Johnson Martin, Flanagan Jack U, Chalmers Silke B, Yoast Ryan E, Kapure Jeevak S, Ross Benjamin P, Vetter Irina, Ashton Mark R, Launikonis Bradley S, Denny William A, Trebak Mohamed, Monteith Gregory R

机构信息

Division of Pharmacy, College of Health and Medicine, University of Tasmania, Hobart, Tasmania 7001, Australia.

Auckland Cancer Society Research Centre, School of Medical Sciences, The University of Auckland, Auckland, 1142, New Zealand.

出版信息

ACS Pharmacol Transl Sci. 2020 Feb 14;3(1):135-147. doi: 10.1021/acsptsci.9b00081. Epub 2020 Jan 13.

DOI:10.1021/acsptsci.9b00081
PMID:32190822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7079732/
Abstract

Store operated calcium (Ca) entry is an important homeostatic mechanism in cells, whereby the release of Ca from intracellular endoplasmic reticulum stores triggers the activation of a Ca influx pathway. Mediated by Orai1, this Ca influx has specific and essential roles in biological processes as diverse as lactation to immunity. Although pharmacological inhibitors of this Ca influx mechanism have helped to define the role of store operated Ca entry in many cellular events, the lack of isoform specific modulators and activators of Orai1 has limited our full understanding of these processes. Here we report the identification and synthesis of an Orai1 activity enhancer that concurrently potentiated Orai1 Ca -dependent inactivation (CDI). This unique enhancer of Orai1 had only a modest effect on Orai3 with weak inhibitory effects at high concentrations in intact MCF-7 breast cancer cells. The Orai1 enhancer heightened vascular smooth muscle cell migration induced by platelet-derived growth factor and the unique store operated Ca entry pathway present in skeletal muscle cells. These studies show that IA65 is an exemplar for the translation and development of Orai isoform selective agents. The ability of IA65 to activate CDI demonstrates that agents can be developed that can enhance Orai1-mediated Ca influx but avoid the cytotoxicity associated with sustained Orai1 activation. IA65 and/or future analogues with similar Orai1 and CDI activating properties could be fine tuners of physiological processes important in specific disease states, such as cellular migration and immune cell function.

摘要

储存性钙(Ca)内流是细胞中一种重要的稳态机制,通过该机制,细胞内内质网储存的Ca释放会触发Ca内流途径的激活。由Orai1介导,这种Ca内流在从泌乳到免疫等多种生物过程中具有特定且重要的作用。尽管这种Ca内流机制的药理学抑制剂有助于确定储存性Ca内流在许多细胞事件中的作用,但缺乏Orai1亚型特异性调节剂和激活剂限制了我们对这些过程的全面理解。在此,我们报告了一种Orai1活性增强剂的鉴定与合成,该增强剂同时增强了Orai1的钙依赖性失活(CDI)。这种独特的Orai1增强剂对Orai3的影响较小,在完整的MCF-7乳腺癌细胞中高浓度时具有微弱的抑制作用。Orai1增强剂增强了血小板衍生生长因子诱导的血管平滑肌细胞迁移以及骨骼肌细胞中存在的独特储存性Ca内流途径。这些研究表明,IA65是Orai亚型选择性药物转化与开发的一个范例。IA65激活CDI的能力表明,可以开发出能够增强Orai1介导的Ca内流但避免与持续Orai1激活相关的细胞毒性的药物。IA65和/或具有类似Orai1和CDI激活特性的未来类似物可能是特定疾病状态下重要生理过程的微调剂,如细胞迁移和免疫细胞功能。