Literature DB >> 12557014

Dementia with Lewy bodies from the perspective of tauopathy.

Eizo Iseki1, Takashi Togo, Kyoko Suzuki, Omi Katsuse, Wami Marui, Rohan de Silva, Andrews Lees, Takayuki Yamamoto, Kenji Kosaka.   

Abstract

We immunohistochemically investigated the prevalence and pattern of phosphorylated tau accumulation in neurons and glia in 46 cases of dementia with Lewy bodies (DLB). Tau-positive neurons composed of neurofibrillary tangles (NFT) and pretangle neurons were found in the hippocampal area in all 46 cases, although the ratio of pretangle neurons in tau-positive neurons was higher in the cases showing low NFT stages. Tau-positive astrocytes were found in the periventricular area in 18 of 46 cases, and partly represented argyrophilic thorn-shaped astrocytes. In contrast, tau-positive oligodendroglia were found in the subcortical white matter in 9 of 46 cases, and represented argyrophilic coiled bodies. Tau-positive argyrophilic grains were found in the hippocampal area in the same cases as those with coiled bodies. The 9 cases with tau-positive coiled bodies and grains were included in the 18 cases with tau-positive astrocytes, and showed larger proportions in the low NFT stages than the 46 cases with tau-positive neurons. Tau-positive neurons were positive both to anti-three-repeat (3R) and -4R tau-specific antibodies, while tau-positive astrocytes, coiled bodies and grains were predominantly positive to anti-4R tau-specific antibody. These tau-positive structures were negative to anti-alpha-synuclein antibody. These findings suggest that the tau accumulation in DLB represents both tau-positive neurons with all six tau isoforms and tau-positive astrocytes, coiled bodies and grains with the 4R tau isoform, and that the different cytoskeletal abnormalities form a link between some neurodegenerative dementing disorders including DLB.

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Year:  2002        PMID: 12557014     DOI: 10.1007/s00401-002-0644-3

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  19 in total

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Review 3.  The Relationships Among Metal Homeostasis, Mitochondria, and Locus Coeruleus in Psychiatric and Neurodegenerative Disorders: Potential Pathogenetic Mechanism and Therapeutic Implications.

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Review 4.  Challenges of multimorbidity of the aging brain: a critical update.

Authors:  Kurt A Jellinger; Johannes Attems
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Review 5.  Interactions Between α-Synuclein and Tau Protein: Implications to Neurodegenerative Disorders.

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Journal:  J Mol Neurosci       Date:  2016-09-15       Impact factor: 3.444

6.  Cerebral amyloid angiopathy in Lewy body disease.

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Review 7.  Interaction between α-synuclein and other proteins in neurodegenerative disorders.

Authors:  Kurt A Jellinger
Journal:  ScientificWorldJournal       Date:  2011-10-24

8.  Tau deposition drives neuropathological, inflammatory and behavioral abnormalities independently of neuronal loss in a novel mouse model.

Authors:  Casey Cook; Silvia S Kang; Yari Carlomagno; Wen-Lang Lin; Mei Yue; Aishe Kurti; Mitsuru Shinohara; Karen Jansen-West; Emilie Perkerson; Monica Castanedes-Casey; Linda Rousseau; Virginia Phillips; Guojun Bu; Dennis W Dickson; Leonard Petrucelli; John D Fryer
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9.  Hippocampal subfield pathologic burden in Lewy body diseases vs. Alzheimer's disease.

Authors:  D G Coughlin; R Ittyerah; C Peterson; J S Phillips; S Miller; K Rascovsky; D Weintraub; A D Siderowf; J E Duda; H I Hurtig; D A Wolk; C T McMillan; P A Yushkevich; M Grossman; E B Lee; J Q Trojanowski; D J Irwin
Journal:  Neuropathol Appl Neurobiol       Date:  2020-09-24       Impact factor: 8.090

10.  Multimodal in vivo and postmortem assessments of tau in Lewy body disorders.

Authors:  David G Coughlin; Jeffrey S Phillips; Emily Roll; Claire Peterson; Rebecca Lobrovich; Katya Rascovsky; Molly Ungrady; David A Wolk; Sandhitsu Das; Daniel Weintraub; Edward B Lee; John Q Trojanowski; Leslie M Shaw; Sanjeev Vaishnavi; Andrew Siderowf; Ilya M Nasrallah; David J Irwin; Corey T McMillan
Journal:  Neurobiol Aging       Date:  2020-08-21       Impact factor: 4.673

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