| Literature DB >> 25787090 |
Ryoko Takeuchi1,2, Yasuko Toyoshima1, Mari Tada1, Hidetomo Tanaka1, Hiroshi Shimizu1, Atsushi Shiga3, Takeshi Miura4, Kenju Aoki4, Akane Aikawa5, Shin Ishizawa5, Takeshi Ikeuchi6, Masatoyo Nishizawa2, Akiyoshi Kakita1, Hitoshi Takahashi1.
Abstract
Amyotrophic lateral sclerosis (ALS) may be accompanied by frontotemporal dementia (FTD). We report a case of glial mixed tau and TDP-43 proteinopathies in a Japanese patient diagnosed clinically as having ALS-D. Autopsy revealed loss of lower motor neurons and degeneration of the pyramidal tracts in the spinal cord and brain stem. The brain showed frontotemporal lobar degeneration (FTLD), the most severe neuronal loss and gliosis being evident in the precentral gyrus. Although less severe, such changes were also observed in other brain regions, including the basal ganglia and substantia nigra. AT8 immunostaining revealed that predominant occurrence of astrocytic tau lesions termed globular astrocytic inclusions (GAIs) was a feature of the affected regions. These GAIs were Gallyas-Braak negative. Neuronal and oligodendrocytic tau lesions were comparatively scarce. pS409/410 immunostaining also revealed similar neuronal and glial TDP-43 lesions. Interestingly, occasional co-localization of tau and TDP-43 was evident in the GAIs. Immunoblot analyses revealed band patterns characteristic of a 4-repeat (4R) tauopathy, corticobasal degeneration and a TDP-43 proteinopathy, ALS/FTLD-TDP Type B. No mutations were found in the MAPT or TDP-43 genes. We consider that this patient harbored a distinct, sporadic globular glial mixed 4R tau and TDP-43 proteinopathy associated with motor neuron disease and FTD.Entities:
Keywords: TDP-43; amyotrophic lateral sclerosis; astrocyte; frontotemporal lobar degeneration; motor neuron disease; tau
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Year: 2015 PMID: 25787090 DOI: 10.1111/bpa.12262
Source DB: PubMed Journal: Brain Pathol ISSN: 1015-6305 Impact factor: 6.508