Immunocytochemical and ultrastructural studies of upper motor neurons in amyotrophic lateral sclerosis |
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Authors: | S. Murayama T. W. Bouldin K. Suzuki |
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Affiliation: | (1) Department of Pathology (Neuropathology), University of North Carolina, CB #7525, Brinkhous-Bullitt Building, 27599-7525 Chapel Hill, NC, USA;(2) Department of Neurophathology, Institute of Brain Research, Faculty of Medicine, The University of Tokyo, Tokyo, Japan |
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Abstract: | Summary The pathological alterations in upper motor neurons were investigated in 27 cases of adult-onset sporadic amyotrophic lateral sclerosis (ALS). No signficant cytoskeletal alterations were found in the Betz cells of any of the cases except one, although cytoskeletal pathology was consistently present in lower motor neurons. The one case had severe circumscribed atrophy of the precentral gyrus and, microscopically, had argentophilic intracytoplasmic inclusions in Betz cells and other pyramidal neurons in the primary motor area as eell as in the lower motor neurons. Immunocytochemically these inclusions contained the epitope of phosphorylated neurofilament and ubiquitin and ultrastructurally consisted of granule-associated filaments with neurofilaments. This is the first demonstration of alterations of cytoskeleton and ubiquitination in the giant cells of Betz, an established subset of upper motor neurons in ALS. Thus, although uncommon, cytoskeletal changes can be found in upper motor neurons in some ALS cases.Supported in part by USPHS grants NS24453, HD03110 and ES01704 |
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Keywords: | Amyotrophic lateral sclerosis Upper motor neurons Ultrastructure Neurofilament Ubiquitin |
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