Network-wide dysregulation of calcium homeostasis in Alzheimer's disease

被引:73
作者
Brawek, Bianca [1 ]
Garaschuk, Olga [1 ]
机构
[1] Univ Tubingen, Inst Physiol 2, D-72074 Tubingen, Germany
关键词
Neurodegeneration; Calcium homeostasis; Hyperexcitability; Glia; Inflammation; NECROSIS-FACTOR-ALPHA; ASTROCYTE GLUTAMATE RELEASE; TRANSGENIC MOUSE MODEL; INNATE IMMUNE-RESPONSE; AMYLOID-BETA; IN-VIVO; MICROGLIAL CELLS; TNF-ALPHA; A-BETA; INTRACELLULAR CALCIUM;
D O I
10.1007/s00441-014-1798-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dysregulation of intracellular Ca2+ homeostasis has been proposed as a common proximal cause of neural dysfunction during aging and Alzheimer's disease (AD). In this context, aberrant Ca2+ signaling has been viewed as a neuronal phenomenon mostly related to the dysfunction of intracellular Ca2+ stores. However, recent data suggest that, in AD, Ca2+ dyshomeostasis is not restricted to neurons but represents a global phenomenon affecting virtually all cells in the brain. AD-related aberrant Ca2+ signaling in astrocytes and microglia, which is activated during the disease, probably contributes profoundly to an inflammatory response that, in turn, impacts neuronal Ca2+ homeostasis and brain function. Based on recent data obtained in vivo and in vitro, we propose that bidirectional interactions between the inflammatory responses of glial cells and aberrant Ca2+ signaling represent a vicious cycle accelerating disease progression.
引用
收藏
页码:427 / 438
页数:12
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