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Granular tau oligomers as intermediates of tau filaments.
Maeda, Sumihiro; Sahara, Naruhiko; Saito, Yuko; Murayama, Miyuki; Yoshiike, Yuji; Kim, Hyonchol; Miyasaka, Tomohiro; Murayama, Shigeo; Ikai, Atsushi; Takashima, Akihiko.
Afiliación
  • Maeda S; Lab for Alzheimer's Disease, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Biochemistry ; 46(12): 3856-61, 2007 Mar 27.
Article en En | MEDLINE | ID: mdl-17338548
Neurofibrillary tangles (NFTs) are pathological hallmarks of several neurodegenerative disorders, including Alzheimer's disease (AD). NFTs are composed of microtubule-binding protein tau, which assembles to form paired helical filaments (PHFs) and straight filaments. Here we show by atomic force microscopy that AD brain tissue and in vitro tau form granular and fibrillar tau aggregates. CD spectral analysis and immunostaining with conformation-dependent antibodies indicated that tau may undergo conformational changes during fibril formation. Enriched granules generated filaments, suggesting that granular tau aggregates may be an intermediate form of tau fibrils. The amount of granular tau aggregates was elevated in prefrontal cortex of Braak stage I cases compared to that of Braak stage 0 cases, suggesting that granular tau aggregation precedes PHF formation. Thus, granular tau aggregates may be a relevant marker for the early diagnosis of tauopathy. Reducing the level of these aggregates may be a promising therapy for tauopathies and for promoting healthy brain aging.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ovillos Neurofibrilares / Proteínas tau Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Biochemistry Año: 2007 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ovillos Neurofibrilares / Proteínas tau Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Biochemistry Año: 2007 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos