A Protein Kinase, PKN, Accumulates in Alzheimer Neurofibrillary Tangles and Associated Endoplasmic Reticulum-Derived Vesicles and Phosphorylates Tau Protein

• Published in: The Journal of neuroscience 1998-09, Vol.18 (18), p.7402-7410
• Main Authors: Kawamata, Toshio, Taniguchi, Taizo, Mukai, Hideyuki, Kitagawa, Michinori, Hashimoto, Takeshi, Maeda, Kiyoshi, Ono, Yoshitaka, Tanaka, Chikako
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Animals; Antibodies; Brain Chemistry - physiology; Cell Compartmentation - physiology; Endoplasmic Reticulum - enzymology; Endoplasmic Reticulum - ultrastructure; Female; Humans; Intracellular Membranes - enzymology; Intracellular Membranes - ultrastructure; Male; Microscopy, Electron; Middle Aged; Neurofibrillary Tangles - enzymology; Neurofibrillary Tangles - pathology; Neurons - enzymology; Neurons - pathology; Neurons - ultrastructure; Phosphorylation; Protein Kinase C - analysis; Protein Kinase C - immunology; Protein Kinase C - metabolism; Rabbits; Subcellular Fractions - enzymology; tau Proteins - metabolism
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.18-18-07402.1998

A possible role for a protein kinase, PKN, a fatty acid-activated serine/threonine kinase with a catalytic domain homologous to the protein kinase C family and a direct target for Rho, was investigated in the pathology of Alzheimer's disease (AD) using a sensitive immunocytochemistry on postmortem human brain tissues and a kinase assay for human tau protein. The present study provides evidences by light, electron, and confocal laser microscopy that in control human brains, PKN is enriched in neurons, where the kinase is concentrated in a subset of endoplasmic reticulum (ER) and ER-derived vesicles localized to the apical compartment of juxtanuclear cytoplasm, as well as late endosomes, multivesicular bodies, Golgi bodies, secretary vesicles, and nuclei. In AD-affected neurons, PKN was redistributed to the cortical cytoplasm and neurites and was closely associated with neurofibrillary tangles (NFTs) and their major constituent, abnormally modified tau. PKN was also found in degenerative neurites within senile plaques. In addition, we report that human tau protein is directly phosphorylated by PKN both in vitro and in vivo. Thus, our results suggest a specific role for PKN in NFT formation and neurodegeneration in AD damaged neurons.