Tau-Tubulin Kinase 1 Expression, Phosphorylation and Co-Localization with Phospho-Ser422 Tau in the Alzheimer's Disease Brain

• Published in: Brain pathology (Zurich, Switzerland) Vol. 23; no. 4; pp. 378 - 389
• Main Authors: Lund, Harald, Cowburn, Richard F., Gustafsson, Elin, Strömberg, Kia, Svensson, Anne, Dahllund, Leif, Malinowsky, David, Sunnemark, Dan
• Format: Journal Article
• Language: English
• Published: Switzerland Blackwell Publishing Ltd 01.07.2013; John Wiley & Sons, Inc; John Wiley and Sons Inc
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - pathology; Alzheimer's disease; Brain - metabolism; Brain - pathology; Dendrites - metabolism; Dendrites - pathology; Female; Gene Expression Regulation - physiology; HEK293 Cells; Humans; Male; Medicin och hälsovetenskap; neurofibrillary tangles; Neurofibrillary Tangles - metabolism; Neurofibrillary Tangles - pathology; Neurons; Neurons - metabolism; Neurons - pathology; Phosphorylation; Phosphorylation - genetics; Protein-Serine-Threonine Kinases - genetics; Protein-Serine-Threonine Kinases - metabolism; RNA, Messenger - metabolism; Serine - metabolism; tau phosphorylation; tau Proteins - genetics; tau Proteins - metabolism; tau-tubulin kinase 1; Transfection
• ISSN: 1015-6305; 1750-3639; 1750-3639
• DOI: 10.1111/bpa.12001

Recent reports have implicated tau‐tubulin kinase 1 (TTBK1) in the pathological phosphorylation of tau that occurs in Alzheimer's disease (AD). The present study was undertaken to provide an extensive characterization of TTBK1 mRNA and protein expression in human brain from AD cases and non‐demented controls so as to better understand the disease relevance of this novel kinase. In situ hybridization and immunohistochemistry revealed abundant expression of TTBK1 in the somatodendritic compartment of cortical and hippocampal neurons of both AD cases and controls. TTBK1 immunoreactivity appeared to vary with the level of phospho‐tau staining, and was strong in the somatodendritic compartment of apparently healthy hippocampal neurons as well as in pre‐tangle neurons where it co‐localized with diffuse phospho‐Ser422 tau staining. Ser422 was confirmed as a TTBK1 substrate in vitro, and an antibody towards the site, in addition to labeling AT8‐positive neurofibrillary tangles (NFTs), neuritic plaques and neuropil threads, also labeled a small population of neurons that were unlabeled with AT8. These data suggest a role for TTBK1 in pre‐tangle formation prior to the formation of fibrillar tau and strengthen the idea that tau is phosphorylated at Ser422 at an early/intermediate stage in NFT formation.