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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.
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页码:425 / 428
页数:4
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