STIM1在神经退行性变中的作用。

Carlos Pascual-Caro, Noelia Espinosa-Bermejo, Eulalia Pozo-Guisado, Francisco Javier Martin-Romero
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引用次数: 11

摘要

STIM1是一种内质网蛋白,在Ca2+动员中起着关键作用。由于其作为内质网管腔内Ca2+传感器的能力,它调节储存操作的Ca2+进入(SOCE),这是一种Ca2+内流途径,涉及真核细胞中的多种信号通路。尽管STIM1在Ca2+转运中发挥着重要作用,但目前对其在神经元中作用的了解要有限得多。越来越多的证据支持STIM1和SOCE在保存长时程增强和记忆形成所需的树突棘中的作用。在这方面,最近的研究表明,STIM1的缺失会损害神经元中Ca2+的动员,从而危及细胞的生存能力,可能是神经退行性疾病的原因。本文讨论了STIM1在神经退行性变中的作用以及低水平STIM1引发细胞死亡的分子基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Role of STIM1 in neurodegeneration.

STIM1 is an endoplasmic reticulum (ER) protein with a key role in Ca2+ mobilization. Due to its ability to act as an ER-intraluminal Ca2+ sensor, it regulates store-operated Ca2+ entry (SOCE), which is a Ca2+ influx pathway involved in a wide variety of signalling pathways in eukaryotic cells. Despite its important role in Ca2+ transport, current knowledge about the role of STIM1 in neurons is much more limited. Growing evidence supports a role for STIM1 and SOCE in the preservation of dendritic spines required for long-term potentiation and the formation of memory. In this regard, recent studies have demonstrated that the loss of STIM1, which impairs Ca2+ mobilization in neurons, risks cell viability and could be the cause of neurodegenerative diseases. The role of STIM1 in neurodegeneration and the molecular basis of cell death triggered by low levels of STIM1 are discussed in this review.

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