Majewski Lukasz, Kuznicki Jacek
International Institute of Molecular and Cell Biology in Warsaw, Trojdena 4, 02-109 Warsaw, Poland.
International Institute of Molecular and Cell Biology in Warsaw, Trojdena 4, 02-109 Warsaw, Poland.
Biochim Biophys Acta. 2015 Sep;1853(9):1940-52. doi: 10.1016/j.bbamcr.2015.01.019. Epub 2015 Jan 31.
In this review we describe the present knowledge about store operated Ca²⁺ entry (SOCE) in neurons and the proteins involved in this process: STIM, as well as Orai and TRP channels. We address the issue of whether SOCE is used only to refill Ca²⁺ in the ER or whether Ca²⁺ that enters the neuronal cell during SOCE also performs signaling functions. We collected the data indicating that SOCE and its components participate in the important processes in neurons. This has implications for identifying new drug targets for the treatment of brain diseases. Evidence indicates that in neurodegenerative diseases Ca²⁺ homeostasis and SOCE components become dysregulated. Thus, different targets and strategies might be identified for the potential treatment of these diseases. This article is part of a Special Issue entitled: 13th European symposium on calcium.
在本综述中,我们描述了目前关于神经元中储存式钙内流(SOCE)以及参与此过程的蛋白质的知识:基质相互作用分子(STIM),以及奥拉帕通道(Orai)和瞬时受体电位通道(TRP)。我们探讨了SOCE是否仅用于补充内质网中的钙,或者在SOCE期间进入神经元细胞的钙是否也具有信号传导功能这一问题。我们收集的数据表明,SOCE及其组成部分参与了神经元中的重要过程。这对于确定治疗脑部疾病的新药物靶点具有重要意义。有证据表明,在神经退行性疾病中,钙稳态和SOCE组成部分会失调。因此,可能会为这些疾病的潜在治疗确定不同的靶点和策略。本文是名为“第13届欧洲钙研讨会”的特刊的一部分。