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Journal article
Ceramide Stabilizes β-Site Amyloid Precursor Protein-cleaving Enzyme 1 and Promotes Amyloid β-Peptide Biogenesis
The Journal of biological chemistry, Vol.278(22), pp.19777-19783
30 May 2003
PMID: 12649271
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
The lipid second messenger ceramide regulates several biochemical events that occur during aging. In addition, its level is highly elevated in the amyloid-burdened brains of Alzheimer's disease patients. Here, we analyzed the impact of aberrant ceramide levels on amyloid β-peptide (Aβ) generation by using a cell-permeable analog of ceramide, C6-ceramide, and several biochemical inhibitors of the sphingomyelin/glycosphingolipid biosynthetic pathway. We found that C6-ceramide increased the biogenesis of Aβ by affecting β-but not γ-cleavage of the amyloid precursor protein. Similarly to C6-ceramide, increased levels of endogenous ceramide induced by neutral sphingomyelinase treatment also promoted the biogenesis of Aβ. Conversely, fumonisin B1, which inhibits the biosynthesis of endogenous ceramide, reduced Aβ production. Exogenous C6-ceramide restored both intracellular ceramide levels and Aβ generation in fumonisin B1-treated cells. These events were specific for amyloid precursor protein and were not associated with apoptotic cell death. Pulse-chase and time-course degradation experiments showed that ceramide post-translationally stabilizes the β-secretase BACE1. Taken together, these data indicate that the lipid second messenger ceramide, which is elevated in the brains of Alzheimer's disease patients, increases the half-life of BACE1 and thereby promotes Aβ biogenesis.
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Details
- Title
- Ceramide Stabilizes β-Site Amyloid Precursor Protein-cleaving Enzyme 1 and Promotes Amyloid β-Peptide Biogenesis
- Creators
- Luigi Puglielli - Harvard UniversityBlake C. Ellis - Harvard Medical SchoolAleister J. Saunders - Massachusetts General HospitalDora M. Kovacs - Harvard University
- Publication Details
- The Journal of biological chemistry, Vol.278(22), pp.19777-19783
- Publisher
- Elsevier
- Number of pages
- 7
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Biology
- Identifiers
- 991021448035904721
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