4.5 Article

14-3-3 eta isoform colocalizes TDP-43 on the coarse granules in the anterior horn cells of patients with sporadic amyotrophic lateral sclerosis

Journal

BRAIN RESEARCH
Volume 1646, Issue -, Pages 132-138

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2016.05.051

Keywords

14-3-3 proteins; Eta isoform; Amyotrophic lateral sclerosis; TDP-43; SNAP25; Anterior horn cells

Categories

Funding

  1. JSPS KAKENHI [26461282]
  2. Grants-in-Aid for Scientific Research [16K14572, 25670427, 25430057, 26461282] Funding Source: KAKEN

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The immunolocalization of the 14-3-3 eta isoform in the anterior horn cells (AHCs) of patients with sporadic amyotrophic lateral sclerosis (ALS) and controls was examined. Compared with the immunolocalization of other 14-3-3 isoforms, the immunolocalization of the 14-3-3 eta isoform was either synaptic at the periphery of AHCs, spindle-shaped in neurites, or granular in the cytoplasm. By double labeling with phosphorylated (p-)TDP-43, the transactivation response DNA binding protein of 43 kDa (TDP-43) demonstrated frequent colocalization of the 14-3-3 eta isoform in granular structures (90%) and spindle-shaped structures (85.4%), but not in p-TDP-43-positive round inclusions. It is speculated that the 14-3-3 eta isoform is associated with not only a synaptic pathology of ALS but also TDP-positive small lesions in the cytoplasm and neurites. The absence of eta-like immunoreactivity in p-TDP-43-positive large inclusions suggests the restricted relevance of the 14-3-3 eta isoform during ALS pathogenesis to some phases of the p-TDP pathology. (C) 2016 Elsevier B.V. All rights reserved.

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