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Myelin injury and degraded myelin vesicles in Alzheimer's disease.

Authors :
Zhan, Xinhua
Zhan, Xinhua
Jickling, Glen C
Ander, Bradley P
Liu, Dazhi
Stamova, Boryana
Cox, Christopher
Jin, Lee-Way
DeCarli, Charles
Sharp, Frank R
Zhan, Xinhua
Zhan, Xinhua
Jickling, Glen C
Ander, Bradley P
Liu, Dazhi
Stamova, Boryana
Cox, Christopher
Jin, Lee-Way
DeCarli, Charles
Sharp, Frank R
Source :
Current Alzheimer research; vol 11, iss 3, 232-238; 1567-2050
Publication Year :
2014

Abstract

ObjectiveMyelin disruption is an important feature of Alzheimer's disease (AD) that contributes to impairment of neuronal circuitry and cognition. In this study we characterize myelin degradation in the brains of patients with Alzheimer's disease compared with normal aged controls.MethodsMyelin from patients with AD (n=13) was compared to matched controls (n=6). Myelin degradation was examined by immunohistochemistry in frontal white matter (WM) for intact myelin basic protein (MBP), degraded MBP, the presence of myelin lipid and for PAS staining. The relationship of myelin degradation and axonal injury was also assessed.ResultsBrains from patients with AD had significant loss of intact MBP, and an increase in degraded MBP in periventricular WM adjacent to a denuded ependymal layer. In regions of myelin degradation, vesicles were identified that stained positive for degraded MBP, myelin lipid, and neurofilament but not for intact MBP. Most vesicles stained for PAS, a corpora amylacea marker. The vesicles were significantly more abundant in the periventricular WM of AD patients compared to controls (44.5 ± 11.0 versus 1.7 ± 1.1, p=0.02).ConclusionIn AD patients degraded MBP is associated in part with vesicles particularly in periventricular WM that is adjacent to areas of ependymal injury.

Details

Database :
OAIster
Journal :
Current Alzheimer research; vol 11, iss 3, 232-238; 1567-2050
Notes :
application/pdf, Current Alzheimer research vol 11, iss 3, 232-238 1567-2050
Publication Type :
Electronic Resource
Accession number :
edsoai.on1377970532
Document Type :
Electronic Resource