Gleevec Inhibits β-Amyloid Production but Not Notch Cleavage

• Published in: Proceedings of the National Academy of Sciences - PNAS 2003-10, Vol.100 (21), p.12444-12449
• Main Authors: Netzer, William J., Dou, Fei, Cai, Dongming, Veach, Darren, Jean, Stephanie, Li, Yueming, Bornmann, William G., Clarkson, Bayard, Xu, Huaxi, Greengard, Paul
• Format: Article
• Language: English
• Subjects: Alzheimers disease; Amyloid beta-Peptides - biosynthesis; Amyloid Precursor Protein Secretases; Animals; Antibodies; Aspartic Acid Endopeptidases; Benzamides; Biological Sciences; Cell culture techniques; Cell free system; Cell Line; Cell lines; Cells, Cultured; Cultured cells; Endopeptidases - metabolism; Enzyme Inhibitors - pharmacology; Female; Fibroblasts; Genes, abl; Guinea Pigs; Imatinib Mesylate; Male; Membrane Proteins - metabolism; Mice; Mice, Knockout; Neurons; Neurons - drug effects; Neurons - metabolism; Neuroscience; Piperazines - pharmacology; Protein-Tyrosine Kinases - antagonists & inhibitors; Proteins; Proto-Oncogene Proteins c-abl - antagonists & inhibitors; Pyrimidines - pharmacology; Rats; Receptor, Notch1; Receptors, Cell Surface; Transcription Factors
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1534745100

$Amyloid\!-\!\beta\>(A\beta)$peptides, consisting mainly of 40 and 42 aa (Aβ 40 and Aβ 42, respectively), are metabolites of the amyloid precursor protein and are believed to be major pathological determinants of Alzheimer's disease. The proteolytic cleavages that form the Aβ N and C termini are catalyzed by β-secretase and γ-secretase, respectively. Here we demonstrate that γ-secretase generation of Aβ in an N2a cell-free system is ATP dependent. In addition, the Abl kinase inhibitor imatinib mesylate (Gleevec, or STI571), which targets the ATP-binding site of Abl and several other tyrosine kinases, potently reduces Aβ production in the N2a cell-free system and in intact N2a cells. Both STI571 and a related compound, inhibitor 2, also reduce Aβ production in rat primary neuronal cultures and in vivo in guinea pig brain. STI571 does not inhibit the γ-secretase-catalyzed S3 cleavage of Notch-1. Furthermore, production of Aβ and its inhibition by STI571 were demonstrated to occur to similar extents in both Abl-/-and WT mouse fibroblasts, indicating that the effect of STI571 on Aβ production does not involve Abl kinase. The efficacy of STI571 in reducing Aβ without affecting Notch-1 cleavage may prove useful as a basis for developing novel therapies for Alzheimer's disease.