| Literature DB >> 20035833 |
Yun-Hyung Choi1, A-Ryeong Gwon, Hye-Young Jeong, Jong-Sung Park, Sang-Ha Baik, Thiruma V Arumugam, Dong-Gyu Jo.
Abstract
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 Ca(2+) signaling, and render cells vulnerable to cell death. In the present study, we demonstrated that Ca(2+)-mediated cell death is functionally associated with gamma-secretase activity. We found that gamma-secretase activity was elevated during Ca(2+)-mediated cell death. Using selective gamma-secretase inhibitors, we examined the role of gamma-secretase in cell death triggered by increased intracellular Ca(2+). Indeed, treatment with the selective gamma-secretase inhibitors, compound E, DAPT, or L-685.458 significantly decreased Ca(2+)-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 Ca(2+)-mediated cell death. (c) 2009 Elsevier Ireland Ltd. All rights reserved.Entities:
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Year: 2009 PMID: 20035833 DOI: 10.1016/j.neulet.2009.12.043
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046