Lysosomal Calcium in Neurodegeneration.

Xinghua Feng, Junsheng Yang
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引用次数: 26

Abstract

Lysosomes are the central organelles responsible for macromolecule recycling in the cell. Lysosomal dysfunction is the primary cause of lysosomal storage diseases (LSDs), and contributes significantly to the pathogenesis of common neurodegenerative diseases. The lysosomes are also intracellular stores for calcium ions, one of the most common second messenger in the cell. Lysosomal Ca2+ is required for diverse cellular processes including signal transduction, vesicular trafficking, autophagy, nutrient sensing, exocytosis, and membrane repair. In this review, we first summarize some recent progresses in the studies of lysosome Ca2+ regulation, with a focus on the newly discovered lysosomal Ca2+ channels and the mechanisms of lysosomal Ca2+ store refilling. We then discuss how defects in lysosomal Ca2+ release and store maintenance cause lysosomal dysfunction and neurodegeneration.

Abstract Image

神经变性中的溶酶体钙。
溶酶体是细胞中负责大分子再循环的中心细胞器。溶酶体功能障碍是溶酶体储存性疾病(LSDs)的主要原因,在常见神经退行性疾病的发病机制中起着重要作用。溶酶体也是细胞内钙离子的储存库,钙离子是细胞中最常见的第二信使之一。溶酶体Ca2+是多种细胞过程所必需的,包括信号转导、囊泡运输、自噬、营养感应、胞吐和膜修复。在这篇综述中,我们首先总结了溶酶体Ca2+调节研究的一些最新进展,重点介绍了新发现的溶酶体Ca2+通道和溶酶体Ca2+储存再填充的机制。然后,我们讨论了溶酶体Ca2+释放和储存维持的缺陷如何导致溶酶体功能障碍和神经退行性变。
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