"Dirty Dancing" of Calcium and Autophagy in Alzheimer's Disease

被引:8
作者
Zhang, Hua [1 ]
Bezprozvanny, Ilya [1 ,2 ]
机构
[1] UT Southwestern Med Ctr, Dept Physiol, Dallas, TX 75390 USA
[2] Peter Great St Petersburg State Polytech Univ, Lab Mol Neurodegenerat, St Petersburg 195251, Russia
来源
LIFE-BASEL | 2023年 / 13卷 / 05期
基金
美国国家卫生研究院; 俄罗斯科学基金会;
关键词
ryanodine receptor; autophagy; calcium signaling; calcineurin; Alzheimer's disease; MOUSE MODEL; LYSOSOMAL CALCIUM; CA2+ RELEASE; DUAL ROLE; RECEPTOR; HOMEOSTASIS; PRESENILINS; CELLS; NEURODEGENERATION; SECRETION;
D O I
10.3390/life13051187
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alzheimer's disease (AD) is the most common cause of dementia. There is a growing body of evidence that dysregulation in neuronal calcium (Ca2+) signaling plays a major role in the initiation of AD pathogenesis. In particular, it is well established that Ryanodine receptor (RyanR) expression levels are increased in AD neurons and Ca2+ release via RyanRs is augmented in AD neurons. Autophagy is important for removing unnecessary or dysfunctional components and long-lived protein aggregates, and autophagy impairment in AD neurons has been extensively reported. In this review we discuss recent results that suggest a causal link between intracellular Ca2+ signaling and lysosomal/autophagic dysregulation. These new results offer novel mechanistic insight into AD pathogenesis and may potentially lead to identification of novel therapeutic targets for treating AD and possibly other neurodegenerative disorders.
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页数:14
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