| Literature DB >> 8592647 |
A Takashima1, H Yamaguchi, K Noguchi, G Michel, K Ishiguro, K Sato, T Hoshino, M Hoshi, K Imahori.
Abstract
Exogenous application of synthetic amyloid beta protein (A beta) is known to induce neurotoxic effects in rat hippocampal culture. We report here that A beta (25-35) induces accumulation of amyloid precursor protein (APP) derivatives in the cytoplasm of neurons. At the same time, the level of the secreted form of APP released into the culture medium decreases. Tau protein kinase I/glycogen synthase kinase-3 beta (TPK I/GSK-3 beta) antisense oligonucleotide blocked APP accumulation and prevented neuronal death. These results provide evidence that APP accumulation after A beta treatment is regulated by TPK I/GSK-3 beta. A beta neurotoxicity is probably mediated via phosphorylation of tau by TPK I/GSK-3 beta, resulting in an impairment of axonal transport, and cytoplasmic accumulation of APP.Entities:
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Year: 1995 PMID: 8592647 DOI: 10.1016/0304-3940(95)11964-x
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046