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The biochemical study on the etiology of Alzheimer’s disease

Alzheimer’s disease has been characterized by senile plaque and neurofibrillary tangle in the brain. However, their relation to etiology of this disease has been left unclear. Recently it has been clarified that neurofibrillay tangle consists of highly phosphorylated tau protein. Then we have starte...

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Detalles Bibliográficos
Autor principal: Imahori, Kazutomo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3417569/
https://www.ncbi.nlm.nih.gov/pubmed/20075608
http://dx.doi.org/10.2183/pjab.86.54
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author Imahori, Kazutomo
author_facet Imahori, Kazutomo
author_sort Imahori, Kazutomo
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description Alzheimer’s disease has been characterized by senile plaque and neurofibrillary tangle in the brain. However, their relation to etiology of this disease has been left unclear. Recently it has been clarified that neurofibrillay tangle consists of highly phosphorylated tau protein. Then we have started to identify the enzyme(s) responsible for this phosphorylation and obtained tau protein kinase I and II. Tau protein kinase I phosphorylated not only tau protein but also pyruvate dehydrogenase, phosphorylation of which caused inactivation of this enzyme and finally led the cell to death. Then we have proved that TPKI is upregulated in AD brain but not in control brain. Upregulation of TPKI was induced by treating the neuronal cells with Aβ protein. Finally we have identified oligomeric aggregation of Aβ protein named Amylospheroid is highly potent to degenerate neuronal cells both in vitro and in vivo systems.
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spelling pubmed-34175692012-11-27 The biochemical study on the etiology of Alzheimer’s disease Imahori, Kazutomo Proc Jpn Acad Ser B Phys Biol Sci Review Alzheimer’s disease has been characterized by senile plaque and neurofibrillary tangle in the brain. However, their relation to etiology of this disease has been left unclear. Recently it has been clarified that neurofibrillay tangle consists of highly phosphorylated tau protein. Then we have started to identify the enzyme(s) responsible for this phosphorylation and obtained tau protein kinase I and II. Tau protein kinase I phosphorylated not only tau protein but also pyruvate dehydrogenase, phosphorylation of which caused inactivation of this enzyme and finally led the cell to death. Then we have proved that TPKI is upregulated in AD brain but not in control brain. Upregulation of TPKI was induced by treating the neuronal cells with Aβ protein. Finally we have identified oligomeric aggregation of Aβ protein named Amylospheroid is highly potent to degenerate neuronal cells both in vitro and in vivo systems. The Japan Academy 2010-01 /pmc/articles/PMC3417569/ /pubmed/20075608 http://dx.doi.org/10.2183/pjab.86.54 Text en © 2010 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Imahori, Kazutomo
The biochemical study on the etiology of Alzheimer’s disease
title The biochemical study on the etiology of Alzheimer’s disease
title_full The biochemical study on the etiology of Alzheimer’s disease
title_fullStr The biochemical study on the etiology of Alzheimer’s disease
title_full_unstemmed The biochemical study on the etiology of Alzheimer’s disease
title_short The biochemical study on the etiology of Alzheimer’s disease
title_sort biochemical study on the etiology of alzheimer’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3417569/
https://www.ncbi.nlm.nih.gov/pubmed/20075608
http://dx.doi.org/10.2183/pjab.86.54
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