Title of article :
High prevalence of thorn-shaped astrocytes in the aged human medial temporal lobe
Author/Authors :
Christian Schultz، نويسنده , , Estifanos Ghebremedhin، نويسنده , , Kelly Del Tredici، نويسنده , , Udo Rüb، نويسنده , , Heiko Braak، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
9
From page :
397
To page :
405
Abstract :
Thorn-shaped astrocytes (TSA) are glial fibrillary tangles that contain abnormally phosphorylated and aggregated microtubule-associated tau protein. The present study examines the prevalence of TSA in the human medial temporal lobe of 100 autopsy brains aged 42–97 years (mean age: 65 years). Serial brain sections were cut at 100 μm and stained using phosphorylation-dependent anti-tau antibodies (AT8, PHF-1, TG3, Alz-50) and silver staining methods for neurofibrillary changes and β-amyloid deposits. TSA preferentially were distributed in periventricular, subependymal, and subpial areas of the mediobasal temporal lobe (MTL). Double-labeling with AT8 and anti-GFAP antibodies demonstrated that the abnormal tau protein was deposited in astroglial cell bodies and in proximal and distal astroglial processes. A pronounced inter-individual variation was noted in the density of AT8-positive TSA, thereby allowing distinction of mild, moderate, and severe involvement. TSA were absent in individuals younger than 60 years. A significant increase in the prevalence of TSA was noted with advancing age. In the age-range of 75–98 years TSA were found in approximately 50% of all individuals. The development of TSA was not correlated with the severity of Alzheimer-related cortical pathology. In summary, this study suggests that TSA is a distinct form of glial tau pathology that occurs with a high frequency in elderly individuals.
Keywords :
Tau-protein , Hyperphosphorylated tau protein , Astrocyte , Glial fibrillary tangles , Alzheimer’s disease , Argyrophilic grain disease
Journal title :
Neurobiology of Aging
Serial Year :
2004
Journal title :
Neurobiology of Aging
Record number :
820414
Link To Document :
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