Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
Kojro, E; Gimpl, G; Lammich, S; Marz, W; Fahrenholz, F.
Low cholesterol stimulates the nonamyloidogenic pathway by its effect on the alpha -secretase ADAM 10.
Proc Natl Acad Sci U S A. 2001; 98(10):5815-5820
Doi: 10.1073/pnas.081612998
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- Co-Autor*innen der Med Uni Graz
- März Winfried
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- Abstract:
- Biochemical, epidemiological, and genetic findings demonstrate a link between cholesterol levels, processing of the amyloid precursor protein (APP), and Alzheimer's disease. In the present report, we identify the alpha-secretase ADAM 10 (a disintegrin and metalloprotease) as a major target of the cholesterol effects on APP metabolism. Treatment of various peripheral and neural cell lines with either the cholesterol-extracting agent methyl-beta-cyclodextrin or the hydroxymethyl glutaryl-CoA reductase inhibitor lovastatin resulted in a drastic increase of secreted alpha-secretase cleaved soluble APP. This strong stimulatory effect was in the range obtained with phorbol esters and was further increased in cells overexpressing ADAM 10. In cells overexpressing APP, the increase of alpha-secretase activity resulted in a decreased secretion of Abeta peptides. Several mechanisms were elucidated as being the basis of enhanced alpha-secretase activity: increased membrane fluidity and impaired internalization of APP were responsible for the effect observed with methyl-beta-cyclodextrin; treatment with lovastatin resulted in higher expression of the alpha-secretase ADAM 10. Our results demonstrate that cholesterol reduction promotes the nonamyloidogenic alpha-secretase pathway and the formation of neuroprotective alpha-secretase cleaved soluble APP by several mechanisms and suggest approaches to prevention of or therapy for Alzheimer's disease.
- Find related publications in this database (using NLM MeSH Indexing)
- ADAM Proteins -
- Amyloid Precursor Protein Secretases -
- Amyloid beta-Protein Precursor - biosynthesis
- Anticholesteremic Agents - pharmacology
- Cell Compartmentation - pharmacology
- Cell Membrane - enzymology
- Cholesterol - metabolism
- Endocytosis - metabolism
- Humans - metabolism
- Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology
- Lovastatin - pharmacology
- Membrane Fluidity - pharmacology
- Membrane Proteins - metabolism
- Metalloendopeptidases - metabolism