Accumulation of insoluble aggregates of beta-amyloid peptide, a cleavage product of amyloid precursor protein, is thought to be a central step in the pathogenesis of Alzheimer's disease. The major enzymes required for the generation of toxic amyloid-beta peptide are beta-(BACE1) and gamma-secretases. Here, we present the rational design and the application of synthetic and lentivirus vector-encoded siRNAs for specific and efficient knockdown of overexpressed and endogenous BACE1, both in dividing and neural stem cells and in a rat brain. We also tested an approach to anti-amyloid therapy by the use of the allele-specific siRNAs to silence the mutant presenilin 1 (L392V PS-1), the main component of gamma-secretase, responsible for development of Familial Alzheimer's disease. Reducing the level of beta-amyloid accumulation in the brain could be beneficial for metabolic studies as well as potential therapeutic approach for prevention and treatment of Alzheimer's disease.
CITATION STYLE
Sierant, M., Kubiak, K., Kazmierczak-Baranska, J., Paduszynska, A., Kuwabara, T., Warashina, M., … Nawrot, B. (2008). RNA interference in silencing of genes of Alzheimer’s disease in cellular and rat brain models. Nucleic Acids Symposium Series (2004), (52), 41–42. https://doi.org/10.1093/nass/nrn021
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