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Astrocyte RNA in relation to neuronal RNA depletion in Alzheimer's disease
Authors:J. A. Doebler  W. R. Markesbery  A. Anthony  S. W. Scheff  R. E. Rhoads
Affiliation:(1) Department of Biochemistry and Sanders-Brown Center on Aging, University of Kentucky, 40536 Lexington, KY, USA;(2) Department of Neurology and Pathology and Sanders-Brown Center on Aging, University of Kentucky, 40536 Lexington, KY, USA;(3) Department of Anatomy and Neurology and Sanders-Brown Center of Aging, University of Kentucky, 40536 Lexington, KY, USA;(4) Department of Biochemistry, University of Kentucky, 40536 Lexington, KY, USA;(5) Department of Biology, The Pennsylvania State University, 16802 University Park, Pennsylvania, USA
Abstract:
Summary A new double-staining procedure, in which the techniques of immunocytochemistry of glial fibrillary acidic protein (GFAP) and quantitative microdensitometry of azure B-RNA were combined, was used to study nucleic acid alterations in fibrous astrocytes in Alzheimer's disease (AD). RNA contents of GFAP-positive cells of the hippocampal endplate (Rose's H3-H5 fields) and the dentate gyrus molecular layer were determined in ten autopsy-proven AD patients (ages 51–88) and ten age-matched, non-demented control. In addition, RNA contents of pyramidal neurons of the endplate were examined. While there were no differences in RNA contents of astrocytes of either region between AD patients and controls, neuronal RNA was markedly depleted. These data suggest that astrocytes maintain protein synthetic capabilities in AD and that RNA loss is limited to the neuronal compartment.Supported by Grants 1P01-AG05119 and 1P50-AG05144 from the National Institutes of Health and by a Small Research Project Award from the University of Kentucky Medical Center
Keywords:Alzheimer's disease  Astrocytes  Glial fibrillary acidic protein  Immunocytochemistry  RNA
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