Department of Integrative Biology and Pharmacology, McGovern Medical School at the University of Texas Health Sciences Center (UTHealth), Houston, TX 77030, USA.
Graduate Program in Biochemistry and Cell Biology, MD Anderson Cancer Center and UTHealth Graduate School of Biomedical Sciences, Houston, TX 77030, USA.
Cells. 2019 Oct 10;8(10):1232. doi: 10.3390/cells8101232.
By influencing Ca homeostasis in spatially and architecturally distinct neuronal compartments, the endoplasmic reticulum (ER) illustrates the notion that form and function are intimately related. The contribution of ER to neuronal Ca homeostasis is attributed to the organelle being the largest reservoir of intracellular Ca and having a high density of Ca channels and transporters. As such, ER Ca has incontrovertible roles in the regulation of axodendritic growth and morphology, synaptic vesicle release, and neural activity dependent gene expression, synaptic plasticity, and mitochondrial bioenergetics. Not surprisingly, many neurological diseases arise from ER Ca dyshomeostasis, either directly due to alterations in ER resident proteins, or indirectly via processes that are coupled to the regulators of ER Ca dynamics. In this review, we describe the mechanisms involved in the establishment of ER Ca homeostasis in neurons. We elaborate upon how changes in the spatiotemporal dynamics of Ca exchange between the ER and other organelles sculpt neuronal function and provide examples that demonstrate the involvement of ER Ca dyshomeostasis in a range of neurological and neurodegenerative diseases.
通过影响空间和结构上不同神经元区室中的钙稳态,内质网(ER)说明了形态和功能密切相关的概念。内质网对神经元钙稳态的贡献归因于该细胞器是细胞内钙的最大储存库,并且具有高密度的钙通道和转运蛋白。因此,内质网钙在调节轴突树突生长和形态、突触小泡释放以及依赖于神经活动的基因表达、突触可塑性和线粒体生物能学方面发挥着不可否认的作用。毫不奇怪,许多神经疾病是由于内质网钙动态失衡引起的,要么是由于内质网驻留蛋白的改变直接引起的,要么是通过与内质网钙动力学调节剂偶联的过程间接引起的。在这篇综述中,我们描述了神经元中内质网钙稳态建立所涉及的机制。我们详细阐述了内质网和其他细胞器之间钙交换的时空动力学变化如何塑造神经元功能,并提供了一些例子,表明内质网钙动态失衡参与了一系列神经和神经退行性疾病。