نتایج جستجو برای: tau protein

تعداد نتایج: 1249886  

2014
Simon Dujardin Katia Lécolle Raphaëlle Caillierez Séverine Bégard Nadège Zommer Cédrick Lachaud Sébastien Carrier Noëlle Dufour Gwennaëlle Aurégan Joris Winderickx Philippe Hantraye Nicole Déglon Morvane Colin Luc Buée

BACKGROUND In sporadic Tauopathies, neurofibrillary degeneration (NFD) is characterised by the intraneuronal aggregation of wild-type Tau proteins. In the human brain, the hierarchical pathways of this neurodegeneration have been well established in Alzheimer's disease (AD) and other sporadic tauopathies such as argyrophilic grain disorder and progressive supranuclear palsy but the molecular an...

Journal: :Investigative ophthalmology & visual science 1993
K U Loeffler D P Edward M O Tso

PURPOSE To characterize the constituents of corpora amylacea in the human retina and optic nerve. METHODS Immunohistochemistry was performed on sections of retina, optic nerve, and brain tissue using antibodies against tau 1, tau-2, and amyloid precursor protein. RESULTS Consistent anti-tau-2 immunoreactivity was noted in the corpora amylacea in the retina, optic nerve, and brain tissue, al...

Journal: :Brain pathology 2007
Eckhard Mandelkow Martin von Bergen Jacek Biernat Eva-Maria Mandelkow

Tau, a major microtubule-associated protein in brain, forms abnormal fibers in Alzheimer's disease and several other neurodegenerative diseases. Tau is highly soluble and adopts a natively unfolded structure in solution. In the paired helical filaments of Alzheimer's disease, small segments of tau adopt a beta-conformation and interact with other tau molecules. In the filament core, the microtu...

Journal: :Science 2010
Keith A Vossel Kai Zhang Jens Brodbeck Aaron C Daub Punita Sharma Steven Finkbeiner Bianxiao Cui Lennart Mucke

Amyloid-β (Aβ) peptides, derived from the amyloid precursor protein, and the microtubule-associated protein tau are key pathogenic factors in Alzheimer's disease (AD). How exactly they impair cognitive functions is unknown. We assessed the effects of Aβ and tau on axonal transport of mitochondria and the neurotrophin receptor TrkA, cargoes that are critical for neuronal function and survival an...

2016
Siân Baker Jürgen Götz

In Alzheimer's disease (AD), the distribution and density of neurofibrillary tangles, a histological hallmark comprised predominately of phosphorylated tau protein, follows a distinct pattern through anatomically connected brain regions. Studies in transgenic mice engineered to regionally confine tau expression have suggested spreading of tau within neural networks. Furthermore, injection of pr...

Journal: :Sheng li xue bao : [Acta physiologica Sinica] 2005
Xiao-Chuan Wang Jing Zhang Xian Yu Liu Han Zhen-Tao Zhou Yao Zhang Jian-Zhi Wang

Hyperphosphorylated microtubule-associated protein tau is the major protein component of neurofibrillary tangles in the brain of patients with Alzheimer's disease (AD). Until now, there is no effective cure to arrest this hyperphosphorylation. The present study was designed to explore the in vivo preventive effect of melatonin on Alzheimer-like tau hyperphosphorylation. Isoproterenol, a beta-re...

2013
Abhinaya Iyer Nichole E. LaPointe Krzysztof Zielke Mariusz Berdynski Elmer Guzman Anna Barczak Małgorzata Chodakowska-Żebrowska Maria Barcikowska Stuart Feinstein Cezary Żekanowski

Over two dozen mutations in the gene encoding the microtubule associated protein tau cause a variety of neurodegenerative dementias known as tauopathies, including frontotemporal dementia (FTD), PSP, CBD and Pick's disease. The vast majority of these mutations map to the C-terminal region of tau possessing microtubule assembly and microtubule dynamics regulatory activities as well as the abilit...

2013
Jürgen Götz Di Xia Gerhard Leinenga Yee Lian Chew Hannah R. Nicholas

TAU is a microtubule-associated protein that under pathological conditions such as Alzheimer's disease (AD) forms insoluble, filamentous aggregates. When 20 years after TAU's discovery the first TAU transgenic mouse models were established, one declared goal that was achieved was the modeling of authentic TAU aggregate formation in the form of neurofibrillary tangles. However, as we review here...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Michel Goedert

T he most common neurodegenerative diseases are characterized by the presence of abnormal filamentous protein inclusions in nerve cells of the brain. In Alzheimer’s disease, these inclusions are made of hyperphosphorylated tau protein (1). Together with the extracellular -amyloid deposits, they constitute the defining neuropathological characteristics of Alzheimer’s disease. Tau inclusions, in ...

Journal: :Neuron 2010
Sang-Won Min Seo-Hyun Cho Yungui Zhou Sebastian Schroeder Vahram Haroutunian William W. Seeley Eric J. Huang Yong Shen Eliezer Masliah Chandrani Mukherjee David Meyers Philip A. Cole Melanie Ott Li Gan

Neurodegenerative tauopathies characterized by hyperphosphorylated tau include frontotemporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) and Alzheimer's disease (AD). Reducing tau levels improves cognitive function in mouse models of AD and FTDP-17, but the mechanisms regulating the turnover of pathogenic tau are unknown. We found that tau is acetylated and that tau acetylation...

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