酸性Ca2+储存在神经变性中。

Emyr Lloyd-Evans
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引用次数: 9

摘要

溶酶体在过去十年中作为Ca2+储存和信号传导的一个非常重要的细胞内位点出现。最近,在溶酶体上发现的具有功能的新离子通道数量有所增加,这些信号通路在基本细胞过程中可能发挥的潜在作用正在被揭示。溶酶体功能缺陷已被证明会导致溶酶体Ca2+稳态的改变,并最终导致细胞死亡。一些神经退行性疾病,从罕见的溶酶体贮积病到更常见的衰老疾病,最近被确定为溶酶体Ca2+稳态的改变,这可能在神经元兴奋毒性和最终细胞死亡中起重要作用。这篇综述将批判性地总结这些最近的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acidic Ca<sup>2+</sup> stores in neurodegeneration.

Acidic Ca<sup>2+</sup> stores in neurodegeneration.

Acidic Ca2+ stores in neurodegeneration.

Lysosomes have emerged in the last decade as an immensely important intracellular site of Ca2+ storage and signalling. More recently there has been an increase in the number of new ion channels found to be functional on lysosomes and the potential roles that these signalling pathways might play in fundamental cellular processes are being uncovered. Defects in lysosomal function have been shown to result in changes in lysosomal Ca2+ homeostasis and ultimately can result in cell death. Several neurodegenerative diseases, from rare lysosomal storage diseases through to more common diseases of ageing, have recently been identified as having alterations in lysosomal Ca2+ homeostasis that may play an important role in neuronal excitotoxicity and ultimately cell death. This review will critically summarise these recent findings.

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