Literature DB >> 8702002

Ultrastructural instability of paired helical filaments from corticobasal degeneration as examined by scanning transmission electron microscopy.

H Ksiezak-Reding1, E Tracz, L S Yang, D W Dickson, M Simon, J S Wall.   

Abstract

Paired helical filaments (PHFs) accumulate in the brains of subjects affected with Alzheimer's disease (AD) and certain other neurodegenerative disorders, including corticobasal degeneration (CBD). Electron microscope studies have shown that PHFs from CBD differ from those of AD by being wider and having a longer periodicity of the helical twist. Moreover, PHFs from CBD have been shown to be primarily composed of two rather than three highly phosphorylated polypeptides of tau (PHF-tau), with these polypeptides expressing no exons 3 and 10. To further explore the relationship between the heterogeneity of PHF-tau and the appearance of abnormal filaments, the ultrastructure and physical parameters such as mass per unit length and dimensions were compared in filaments from CBD and AD using high resolution scanning transmission electron microscopy (STEM). Filament-enriched fractions were isolated as Sarcosyl-insoluble pellets and for STEM studies, samples were freeze-dried without prior fixation or staining. Ultrastructurally, PHFs from CBD were shown to be a heterogeneous population as double- and single-stranded filaments could be identified based on their width and physical mass per unit length expressed in kilodaltons (kd) per nanometer (nm). Less abundant, double-stranded filaments had a maximal width of 29 nm and a mass per unit length of 133 kd/nm, whereas three times more abundant single-stranded filaments were 15 nm wide and bad a mass per unit length of 62 kd/nm. Double-stranded filaments also displayed a distinct axial region of less dense mass, which appeared to divide the PHFs into two protofilament-like strands. Furthermore, these filaments were frequently observed to physically separate along the long axis into two single strands or to break longitudinally. In contrast, PHFs from AD were ultrastructurally stable and uniform both in their width (22 nm) and physical mass per unit length (104 kd/nm). The ultrastructural features indicate that filaments of CBD and AD differ both in stability and packing of tau and that CBD filaments, composed of two distinct protofilaments, are more labile under STEM conditions. As fixed and stained filaments from CBD have been shown to be stable and uniform in size by conventional transmission electron microscopy, STEM studies may be particularly suitable for detecting instability of unstained and unfixed filaments. The results also suggest that molecular heterogeneity and/or post-translational modifications of tau may strongly influence the morphology and stability of abnormal filaments.

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Year:  1996        PMID: 8702002      PMCID: PMC1865307     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  53 in total

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Authors:  M KIDD
Journal:  Nature       Date:  1963-01-12       Impact factor: 49.962

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Authors:  M Butler; M L Shelanski
Journal:  J Neurochem       Date:  1986-11       Impact factor: 5.372

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Authors:  H Braak; E Braak; I Grundke-Iqbal; K Iqbal
Journal:  Neurosci Lett       Date:  1986-04-24       Impact factor: 3.046

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Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

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Journal:  Annu Rev Biophys Biophys Chem       Date:  1986

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Authors:  S Takauchi; M Hosomi; S Marasigan; M Sato; S Hayashi; K Miyoshi
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8.  Substructures of paired helical filaments from Alzheimer's disease neurofibrillary tangles.

Authors:  H M Wisniewski; G Y Wen
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

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Journal:  Lancet       Date:  1986-11-22       Impact factor: 79.321

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Journal:  EMBO J       Date:  1985-12-30       Impact factor: 11.598

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  9 in total

1.  Structural analysis of Pick's disease-derived and in vitro-assembled tau filaments.

Authors:  M E King; N Ghoshal; J S Wall; L I Binder; H Ksiezak-Reding
Journal:  Am J Pathol       Date:  2001-04       Impact factor: 4.307

Review 2.  Amyloid structure and assembly: insights from scanning transmission electron microscopy.

Authors:  Claire Goldsbury; Ulrich Baxa; Martha N Simon; Alasdair C Steven; Andreas Engel; Joseph S Wall; Ueli Aebi; Shirley A Müller
Journal:  J Struct Biol       Date:  2010-09-22       Impact factor: 2.867

3.  Clustering and spatial correlations of the neuronal cytoplasmic inclusions, astrocytic plaques and ballooned neurons in corticobasal degeneration.

Authors:  R A Armstrong; N J Cairns
Journal:  J Neural Transm (Vienna)       Date:  2009-06-24       Impact factor: 3.575

4.  Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments.

Authors:  M G Spillantini; M Goedert; R A Crowther; J R Murrell; M R Farlow; B Ghetti
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

5.  Posttranslational Modifications Mediate the Structural Diversity of Tauopathy Strains.

Authors:  Tamta Arakhamia; Christina E Lee; Yari Carlomagno; Duc M Duong; Sean R Kundinger; Kevin Wang; Dewight Williams; Michael DeTure; Dennis W Dickson; Casey N Cook; Nicholas T Seyfried; Leonard Petrucelli; Anthony W P Fitzpatrick
Journal:  Cell       Date:  2020-02-06       Impact factor: 41.582

6.  Tau Protein and Frontotemporal Dementias.

Authors:  Michel Goedert; Maria Grazia Spillantini; Benjamin Falcon; Wenjuan Zhang; Kathy L Newell; Masato Hasegawa; Sjors H W Scheres; Bernardino Ghetti
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

Review 7.  Clinicopathologic assessment and imaging of tauopathies in neurodegenerative dementias.

Authors:  Melissa E Murray; Naomi Kouri; Wen-Lang Lin; Clifford R Jack; Dennis W Dickson; Prashanthi Vemuri
Journal:  Alzheimers Res Ther       Date:  2014-01-02       Impact factor: 6.982

8.  Novel tau filament fold in corticobasal degeneration.

Authors:  Wenjuan Zhang; Airi Tarutani; Kathy L Newell; Alexey G Murzin; Tomoyasu Matsubara; Benjamin Falcon; Ruben Vidal; Holly J Garringer; Yang Shi; Takeshi Ikeuchi; Shigeo Murayama; Bernardino Ghetti; Masato Hasegawa; Michel Goedert; Sjors H W Scheres
Journal:  Nature       Date:  2020-02-12       Impact factor: 49.962

Review 9.  Prion-Like Propagation Mechanisms in Tauopathies and Traumatic Brain Injury: Challenges and Prospects.

Authors:  Hadeel Alyenbaawi; W Ted Allison; Sue-Ann Mok
Journal:  Biomolecules       Date:  2020-10-27
  9 in total

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