Contribution of γ-secretase to calcium-mediated cell death

被引:8
|
作者
Choi, Yun-Hyung [1 ]
Gwon, A-Ryeong [1 ]
Jeong, Hye-Young [1 ]
Park, Jong-Sung [1 ]
Baik, Sang-Ha [1 ]
Arumugam, Thiruma V. [2 ]
Jo, Dong-Gyu [1 ]
机构
[1] Sungkyunkwan Univ, Coll Pharm, Suwon 440746, South Korea
[2] Univ Queensland, Sch Biomed Sci, Brisbane, Qld 4072, Australia
关键词
gamma-Secretase; Alzheimer's disease; Calcium; Cell death; ALZHEIMERS-DISEASE; CALSENILIN/DREAM/KCHIP3; APOPTOSIS; PATHWAYS; NOTCH;
D O I
10.1016/j.neulet.2009.12.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Presenilins are the catalytic subunit of the large gamma-secretase complex, that promotes intramembranous proteolysis of the beta-amyloid precursor protein (APP), resulting in the production of beta-amyloid (A beta). Mutant presenilin causes early-onset familial Alzheimer's disease (FAD), is related to abnormal Ca2+ signaling, and render cells vulnerable to cell death. In the present study, we demonstrated that Ca2+-mediated cell death is functionally associated with gamma-secretase activity. We found that gamma-secretase activity was elevated during Ca2+-mediated cell death. Using selective gamma-secretase inhibitors, we examined the role of gamma-secretase in cell death triggered by increased intracellular Ca2+. Indeed, treatment with the selective gamma-secretase inhibitors, compound E, DAFT, or L-685.458 significantly decreased Ca2+-triggered cell death with that of the controls, but did not affect staurosporin or tunicamycin-mediated cell death. These results implicate the role of gamma-secretase activity in Ca2+-ediated cell death. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:425 / 428
页数:4
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