Literature DB >> 2557644

Tau and ubiquitin immunoreactivity at different stages of formation of Alzheimer neurofibrillary tangles.

C Bancher1, C Brunner, H Lassmann, H Budka, K Jellinger, F Seitelberger, I Grundke-Iqbal, K Iqbal, H M Wisniewski.   

Abstract

In his original 1911 publication Alois Alzheimer classified neurofibrillary tangles (ANT) into three morphologically defined subgroups according to their stage of maturation. The present study shows that changes in the morphological appearance of ANT during their maturation process are accompanied by changes in their antigenic profile. As shown by several immunocytochemical studies these abnormal phosphorylated microtubule-associated protein tau and of ubiquitin. In this study, immunoreactivity for the altered tau is not only seen in a subset of tangles but also in the cytoplasm of some nerve cells lacking ANT, which we believe to be at a stage of neuronal alteration preceding the formation of compact tangles (Stage 0 tangles). Similar numbers of Stage 0 tangles are present in the brains of age-matched non-demented individuals as in Alzheimer cases, but are absent in young controls lacking ANT. In extracellular "ghost tangles", the ultimate stage of neurofibrillary degeneration, immunoreactivity for tau is accessible to antibodies only when tissue sections are pretreated with formic acid to uncover the binding sites. In contrast to tau, presence/accessibility of an epitope residing on residues 50-65 of ubiquitin recognized by a monoclonal antibody raised to paired helical filaments (3-39) increases during the maturation of ANT and is most pronounced in "ghost tangles". Appearance/uncovering of the 3-39 epitope and masking of tau reactivity during tangle maturation may reflect degradation or conformational changes in the pathological filaments due to their aging and the final loss of their parent nerve cells.

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Year:  1989        PMID: 2557644

Source DB:  PubMed          Journal:  Prog Clin Biol Res        ISSN: 0361-7742


  18 in total

1.  Expression of human apolipoprotein E4 in neurons causes hyperphosphorylation of protein tau in the brains of transgenic mice.

Authors:  I Tesseur; J Van Dorpe; K Spittaels; C Van den Haute; D Moechars; F Van Leuven
Journal:  Am J Pathol       Date:  2000-03       Impact factor: 4.307

2.  Tau gene transfer, but not alpha-synuclein, induces both progressive dopamine neuron degeneration and rotational behavior in the rat.

Authors:  Ronald L Klein; Robert D Dayton; Wen-Lang Lin; Dennis W Dickson
Journal:  Neurobiol Dis       Date:  2005-10       Impact factor: 5.996

3.  Link between DYRK1A overexpression and several-fold enhancement of neurofibrillary degeneration with 3-repeat tau protein in Down syndrome.

Authors:  Jerzy Wegiel; Wojciech Kaczmarski; Madhabi Barua; Izabela Kuchna; Krzysztof Nowicki; Kuo-Chiang Wang; Jarek Wegiel; Shuang Ma Yang; Janusz Frackowiak; Bozena Mazur-Kolecka; Wayne P Silverman; Barry Reisberg; Isabel Monteiro; Mony de Leon; Thomas Wisniewski; Arthur Dalton; Florence Lai; Yu-Wen Hwang; Tatyana Adayev; Fei Liu; Khalid Iqbal; Inge-Grundke Iqbal; Cheng-Xin Gong
Journal:  J Neuropathol Exp Neurol       Date:  2011-01       Impact factor: 3.685

4.  Tau accumulation activates the unfolded protein response by impairing endoplasmic reticulum-associated degradation.

Authors:  Jose F Abisambra; Umesh K Jinwal; Laura J Blair; John C O'Leary; Qingyou Li; Sarah Brady; Li Wang; Chantal E Guidi; Bo Zhang; Bryce A Nordhues; Matthew Cockman; Amirthaa Suntharalingham; Pengfei Li; Ying Jin; Christopher A Atkins; Chad A Dickey
Journal:  J Neurosci       Date:  2013-05-29       Impact factor: 6.167

5.  Immunohistochemical analysis of ubiquilin-1 in the human hippocampus: association with neurofibrillary tangle pathology.

Authors:  Katsuyoshi Mizukami; Eric E Abrahamson; Zhiping Mi; Masanori Ishikawa; Kazushi Watanabe; Setsuo Kinoshita; Takashi Asada; Milos D Ikonomovic
Journal:  Neuropathology       Date:  2013-07-21       Impact factor: 1.906

6.  Hyperphosphorylated tau in parahippocampal cortex impairs place learning in aged mice expressing wild-type human tau.

Authors:  Tetsuya Kimura; Shunji Yamashita; Tetsuya Fukuda; Jun-Mi Park; Miyuki Murayama; Tatsuya Mizoroki; Yuji Yoshiike; Naruhiko Sahara; Akihiko Takashima
Journal:  EMBO J       Date:  2007-11-15       Impact factor: 11.598

Review 7.  Cytosolic abnormally hyperphosphorylated tau but not paired helical filaments sequester normal MAPs and inhibit microtubule assembly.

Authors:  Khalid Iqbal; Alejandra del C Alonso; Inge Grundke-Iqbal
Journal:  J Alzheimers Dis       Date:  2008-08       Impact factor: 4.472

Review 8.  [Post-mortem diagnosis of Alzheimer's disease].

Authors:  D R Thal; H Braak
Journal:  Pathologe       Date:  2005-05       Impact factor: 1.011

9.  Characterization of Early Pathological Tau Conformations and Phosphorylation in Chronic Traumatic Encephalopathy.

Authors:  Nicholas M Kanaan; Kristine Cox; Victor E Alvarez; Thor D Stein; Sharra Poncil; Ann C McKee
Journal:  J Neuropathol Exp Neurol       Date:  2016-01       Impact factor: 3.685

10.  Effect of neocortical and hippocampal amyloid deposition upon galaninergic and cholinergic neurites in AβPPswe/PS1ΔE9 mice.

Authors:  Christy M Kelley; Sylvia E Perez; Cassia R Overk; David Wynick; Elliott J Mufson
Journal:  J Alzheimers Dis       Date:  2011       Impact factor: 4.472

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