Literature DB >> 21175864

Enhancement of native and phosphorylated TDP-43 immunoreactivity by proteinase K treatment following autoclave heating.

Fumiaki Mori1, Kunikazu Tanji, Akiyoshi Kakita, Hitoshi Takahashi, Koichi Wakabayashi.   

Abstract

TDP-43 is a major disease protein in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TDP-43 (FTLD-TDP). To evaluate the effectiveness of proteinase K (PK) treatment in antigen retrieval for native and phosphorylated TDP-43 protein, we examined the temporal cortex and spinal cord from patients with sporadic ALS and FTLD-TDP and control subjects. PK treatment following heat retrieval enhanced the immunoreactivity for native TDP-43 in controls as well as for native and phosphorylated TDP-43 in ALS and FTLD-TDP. A significant number of TDP-43-positive neuropil threads were demonstrated in lesions, in which routine immunohistochemistry revealed that the predominant inclusions are cytoplasmic. This retrieval method is the best of immunohistochemical techniques for demonstrating TDP-43 pathology, especially in the neuropil.
© 2010 Japanese Society of Neuropathology.

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Year:  2010        PMID: 21175864     DOI: 10.1111/j.1440-1789.2010.01184.x

Source DB:  PubMed          Journal:  Neuropathology        ISSN: 0919-6544            Impact factor:   1.906


  1 in total

1.  Phosphorylated TDP-43 aggregates in skeletal and cardiac muscle are a marker of myogenic degeneration in amyotrophic lateral sclerosis and various conditions.

Authors:  Fumiaki Mori; Mari Tada; Tomoya Kon; Yasuo Miki; Kunikazu Tanji; Hidekachi Kurotaki; Masahiko Tomiyama; Tomohiko Ishihara; Osamu Onodera; Akiyoshi Kakita; Koichi Wakabayashi
Journal:  Acta Neuropathol Commun       Date:  2019-10-28       Impact factor: 7.801

  1 in total

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