Abstract
The mature form of Alzheimer's beta-amyloid precursor protein (APP) is phosphorylated specifically at Thr(668) in neurons. In mature neurons, phosphorylated APP is detected in neurites, with dephosphorylated APP being found mostly in the cell body. In vitro, active cyclin-dependent kinase 5 (Cdk5) phosphorylated the cytoplasmic domain of APP at Thr(668). Treatment of mature neurons with an antisense oligonucleotide to Cdk5 suppressed Cdk5 expression and significantly diminished the level of phosphorylated APP. The expression of APP was unaffected in antisense-treated neurons. These results indicate that in neurons APP is phosphorylated by Cdk5, and that this may play a role in its localization.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amyloid beta-Protein Precursor / chemistry
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Amyloid beta-Protein Precursor / genetics
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Amyloid beta-Protein Precursor / metabolism*
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Animals
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Brain / metabolism*
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Cyclin-Dependent Kinase 5
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Cyclin-Dependent Kinases / metabolism*
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Embryo, Mammalian
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Hippocampus / embryology
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Hippocampus / metabolism
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Lung / metabolism
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Male
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Mice
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Mice, Inbred C57BL
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Neurons / cytology
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Neurons / drug effects
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Neurons / metabolism*
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Oligodeoxyribonucleotides, Antisense / pharmacology
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Organ Specificity
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Phosphorylation
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Rats
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Rats, Wistar
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Spleen / metabolism
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Testis / metabolism
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Threonine
Substances
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Amyloid beta-Protein Precursor
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Oligodeoxyribonucleotides, Antisense
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Threonine
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Cyclin-Dependent Kinase 5
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Cdk5 protein, mouse
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Cdk5 protein, rat
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Cyclin-Dependent Kinases