Journal
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
Volume 60, Issue 5, Pages 441-448Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1093/jnen/60.5.441
Keywords
Alzheimer disease; lectins; O-glycosylation; sialic acid; specific lectins; sprouting neurons; T antigen
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Reactive plasticity, including axonal and dendritic sprouting and reactive synaptogenesis. has been proposed to contribute to the pathogenesis of several neurological disorders. This work was aimed at identifying the possible role of protein glycosylation in the brain from patients with Alzheimer disease (AD), using lectin histochemistry, as determinants of reactive plasticity. Results indicate an increase in the production of cryptic O-glycosidically linked proteins (NeuAc alpha2,6 Gal beta1,3GalNA alpha1.0 Ser/Thr or sialyl-T-antigen) in neuritic sprouting in AD brains as determined by positive labeling with Amaranthus leucocarpus (ALL, T-antigen-specific) and Macrobrachium rosenbergii (MRL, specific for NeuAc5,9Ac(2)) lectins. Immunohistochemistry indicated that lectin staining was specific for the synaptic sprouting process (megancurites) in AD. These results were confirmed using anti-synaptophysin and anti-GAP 43 antibodies, which recognized megancurites and dystrophic neurites around amyloid-beta deposits. In normal control brains, labeling with the aforementioned lectins was restricted to microvessels. Control experiments with neurarninidase-treated brain samples revealed positivity to the lectin front Arachis hypogaea (PNA), which is specific fur galactose. Our results suggest specific O-glycosylation patterns of proteins closely related to neuronal plasticity in AD.
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