Ca2+ dysregulation in the endoplasmic reticulum related to Alzheimer's disease: A review on experimental progress and computational modeling

被引:24
作者
Liang, Jingyi [1 ,2 ]
Kulasiri, Don [1 ,2 ]
Samarasinghe, Sandhya [1 ,3 ]
机构
[1] Lincoln Univ, Ctr Adv Computat Solut C fACS, Christchurch, New Zealand
[2] Lincoln Univ, Dept Mol Biosci, Christchurch, New Zealand
[3] Lincoln Univ, Dept Informat & Enabling Technol, Christchurch, New Zealand
关键词
Alzheimer's disease; Endoplasmic reticulum; Ca2+ dysregulation; Amyloid-beta; Systems biology; Computational modeling; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; CALHM1 P86L POLYMORPHISM; CALCIUM WAVE-PROPAGATION; BETA-AMYLOID PEPTIDES; D-ASPARTATE RECEPTORS; RYANODINE RECEPTOR; INTRACELLULAR CALCIUM; OXIDATIVE STRESS; KINETIC-MODEL; TRISPHOSPHATE RECEPTOR;
D O I
10.1016/j.biosystems.2015.05.003
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 a devastating, incurable neurodegenerative disease affecting millions of people worldwide. Dysregulation of intracellular Ca2+ signaling has been observed as an early event prior to the presence of clinical symptoms of AD and is believed to be a crucial factor contributing to its pathogenesis. The progressive and sustaining increase in the resting level of cytosolic Ca2+ will affect downstream activities and neural functions. This review focuses on the issues relating to the increasing Ca2+ release from the endoplasmic reticulum (ER) observed in AD neurons. Numerous research papers have suggested that the dysregulation of ER Ca2+ homeostasis is associated with mutations in the presenilin genes and amyloid-beta oligomers. These disturbances could happen at many different points in the signaling process, directly affecting ER Ca2+ channels or interfering with related pathways, which makes it harder to reveal the underlying mechanisms. This review paper also shows that computational modeling is a powerful tool in Ca2+ signaling studies and discusses the progress in modeling related to Ca2+ dysregulation in AD research. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 15
页数:15
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