Journal of the Neurological Sciences
Volume 208, Issue 1 , Pages 17-24, 15 April 2003

Association of phosphorylation site of tau protein with neuronal apoptosis in Alzheimer's disease

  • Katsuji Kobayashi

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +81-76-265-2301; fax: +81-76-234-4254.
    • Department of Psychiatry and Neurobiology, Graduate School of Medical Sciences, Kanazawa University, 13-1, Takara-machi, Kanazawa, Ishikawa 920-8641, Japan
  • ,
  • Hiroyuki Nakano

      Affiliations

    • Department of Psychiatry and Neurobiology, Graduate School of Medical Sciences, Kanazawa University, 13-1, Takara-machi, Kanazawa, Ishikawa 920-8641, Japan
  • ,
  • Masahiro Hayashi

      Affiliations

    • National Sanatorium Hokuriku Hospital, Nobusue, Jouhana-machi, Toyama, Japan
  • ,
  • Masao Shimazaki

      Affiliations

    • Department of Psychiatry and Neurobiology, Graduate School of Medical Sciences, Kanazawa University, 13-1, Takara-machi, Kanazawa, Ishikawa 920-8641, Japan
  • ,
  • Yuken Fukutani

      Affiliations

    • Department of Psychiatry, Fukui Medical University, Matsuoka-tyou, Fukui, Japan
  • ,
  • Kazuo Sasaki

      Affiliations

    • Department of Psychiatry, Fukui Medical University, Matsuoka-tyou, Fukui, Japan
  • ,
  • Kaoru Sugimori

      Affiliations

    • Department of Psychiatry and Neurobiology, Graduate School of Medical Sciences, Kanazawa University, 13-1, Takara-machi, Kanazawa, Ishikawa 920-8641, Japan
  • ,
  • Yoshifumi Koshino

      Affiliations

    • Department of Psychiatry and Neurobiology, Graduate School of Medical Sciences, Kanazawa University, 13-1, Takara-machi, Kanazawa, Ishikawa 920-8641, Japan

Received 17 June 2002; received in revised form 16 October 2002; accepted 16 October 2002.

Abstract 

In addition to neuritic changes and amyloid deposits, neuronal and glial cell apoptosis is an important pathological feature of Alzheimer's disease (AD). Several factors have been postulated as causes or triggers of cellular apoptotic change. This study focused on a quantifiable relationship between phosphorylation sites of tau protein in the neurofibrillary tangles (NFT) and neuronal apoptosis. Five monoclonal anti-tau antibodies (AT180, AT8, HT7, Tau2 and Tau5) for NFT labeling and TdT-mediated UTP nick-end labeling (TUNEL) for localizing apoptotic change were employed. TUNEL-stained neuronal nuclei showed significantly high density in the entorhinal cortex, cornu ammonis (CA) and the parietal cortex. In all regions, density of TUNEL-stained neuronal nuclei showed significantly direct correlation with that of AT8-, AT180- and Tau2-positive neurons. Correlation of TUNEL-stained neuronal nuclei with tau-positive neurons differed depending on the cerebral regions. Density of TUNEL-stained neuronal nuclei showed inverse correlation with that of both AT8-positive and Gallyas-stained NFT in the CA and showed significantly direct correlation with AT8- and HT7-positive neurons in the frontal cortex. Density of tau-positive and Gallyas-stained NFT was higher than that of TUNEL-stained nuclei. We conclude that phosphorylation sites of tau, 159–163 and 202–205, are probably associated with neuronal apoptosis and apoptotic change follows abnormal phosphorylation of tau.

Keywords:  Neurofibrillary tangles, Apoptosis, TUNEL, Alzheimer's disease, Pretangle neurons

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PII: S0022-510X(02)00410-0

doi:10.1016/S0022-510X(02)00410-0

Journal of the Neurological Sciences
Volume 208, Issue 1 , Pages 17-24, 15 April 2003