Pathogenesis of alzheimer-related neuritic plaques: AT8 immunoreactive dystrophic neurites precede argyrophilic neurites in plaques of the entorhinal region, hippocampal formation, and amygdala

D. M. Yilmazer-Hanke

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10 Citations (Scopus)

Abstract

The hyperphosphorylated microtubule-associated protein tau is a major component of Alzheimer-related intraneuronal cytoskeletal changes. Hyperphosphorylated tau proteins may form straight and paired helical filaments, which can condensate and crosslink, leading to agglomerations called neurofibrillary changes. The non-crosslinked filaments have been shown to precede the neurofibrillary changes in the Cell body and dendritic processes of neurons. However, Alzheimer-related cytoskeletal changes are also found in dystrophic neurites of axonal origin. In the present study, occurrence of non-crosslinked and crosslinked cytoskeletal changes in dystrophic neurites of plaques has been investigated in the entorhinal region, hippocampal formation, and amygdala of cases at transentorhinal and limbic stages according to Braak and Braak. Consecutive 7 μm thick paraffin sections have been stained with the Campbell/Switzer and Gallyas silver techniques, as well as AT8 antibody for demonstration of β-amyloid deposits, neurofibrillary changes, and non-crosslinked filaments, respectively. Most β-amyloid deposits contained neither AT8-immunoreactive nor Gallyas positive argyrophilic neurites. Furthermore, a considerable proportion of β-amyloid deposits displayed only AT8-immunoreactive dystrophic neurites. The findings indicate that AT8-immunoreactive neuronal processes located in β-amyloid deposits precede Gallyas positive argyrophilic neurites in neuritic plaques. Both non-crosslinked and crosslinked forms of Alzheimer-type cytoskeletal changes are likely to develop in β-amyloid deposits.

Original languageEnglish
Pages (from-to)194-198
Number of pages5
JournalClinical Neuropathology
Volume17
Issue number4
StatePublished - Jul 1998
Externally publishedYes

Fingerprint

Amyloid Plaques
Neurites
Amygdala
Hippocampus
tau Proteins
Microtubule-Associated Proteins
Silver
Paraffin
Neurons
Antibodies

All Science Journal Classification (ASJC) codes

  • Clinical Neurology
  • Pathology and Forensic Medicine
  • Neuroscience(all)

Cite this

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title = "Pathogenesis of alzheimer-related neuritic plaques: AT8 immunoreactive dystrophic neurites precede argyrophilic neurites in plaques of the entorhinal region, hippocampal formation, and amygdala",
abstract = "The hyperphosphorylated microtubule-associated protein tau is a major component of Alzheimer-related intraneuronal cytoskeletal changes. Hyperphosphorylated tau proteins may form straight and paired helical filaments, which can condensate and crosslink, leading to agglomerations called neurofibrillary changes. The non-crosslinked filaments have been shown to precede the neurofibrillary changes in the Cell body and dendritic processes of neurons. However, Alzheimer-related cytoskeletal changes are also found in dystrophic neurites of axonal origin. In the present study, occurrence of non-crosslinked and crosslinked cytoskeletal changes in dystrophic neurites of plaques has been investigated in the entorhinal region, hippocampal formation, and amygdala of cases at transentorhinal and limbic stages according to Braak and Braak. Consecutive 7 μm thick paraffin sections have been stained with the Campbell/Switzer and Gallyas silver techniques, as well as AT8 antibody for demonstration of β-amyloid deposits, neurofibrillary changes, and non-crosslinked filaments, respectively. Most β-amyloid deposits contained neither AT8-immunoreactive nor Gallyas positive argyrophilic neurites. Furthermore, a considerable proportion of β-amyloid deposits displayed only AT8-immunoreactive dystrophic neurites. The findings indicate that AT8-immunoreactive neuronal processes located in β-amyloid deposits precede Gallyas positive argyrophilic neurites in neuritic plaques. Both non-crosslinked and crosslinked forms of Alzheimer-type cytoskeletal changes are likely to develop in β-amyloid deposits.",
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