Lysosomal Calcium in Neurodegeneration.

Xinghua Feng, Junsheng Yang
{"title":"Lysosomal Calcium in Neurodegeneration.","authors":"Xinghua Feng,&nbsp;Junsheng Yang","doi":"10.1166/msr.2016.1055","DOIUrl":null,"url":null,"abstract":"<p><p>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 Ca<sup>2+</sup> 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 Ca<sup>2+</sup> regulation, with a focus on the newly discovered lysosomal Ca<sup>2+</sup> channels and the mechanisms of lysosomal Ca<sup>2+</sup> store refilling. We then discuss how defects in lysosomal Ca<sup>2+</sup> release and store maintenance cause lysosomal dysfunction and neurodegeneration.</p>","PeriodicalId":74176,"journal":{"name":"Messenger (Los Angeles, Calif. : Print)","volume":"5 1-2","pages":"56-66"},"PeriodicalIF":0.0000,"publicationDate":"2016-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1166/msr.2016.1055","citationCount":"26","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Messenger (Los Angeles, Calif. : Print)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1166/msr.2016.1055","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Inositol 1,4,5-trisphosphate Receptor Mutations associated with Human Disease. The Making and Breaking of Inositol 1,4,5-Trisphosphate Receptor Tetramers. CD38 in the Nucleus Accumbens is Critical in Paternal Behavior in Mice TRPM2, a New Player, in Cyclic ADP-Ribose/CD38-Dependent Oxytocin Release in the Hypothalamus A Ca2+-Calmodulin-Dependent Protein Kinase II Inhibitor Suppresses Cell Migration of CD38-Expressing Human Embryonic Kidney Cells: A Preliminary Report
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1