Title of article :
3D-Reconstruction of microglia and amyloid in APP23 transgenic mice: no evidence of intracellular amyloid
Author/Authors :
M. Stalder، نويسنده , , T. Deller، نويسنده , , M. Staufenbiel، نويسنده , , M. Jucker، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
8
From page :
427
To page :
434
Abstract :
Microglia cells are closely associated with compact amyloid plaques in Alzheimer’s disease (AD) brains. Although activated microglia seem to play a central role in the pathogenesis of AD, mechanisms of microglial activation by β-amyloid as well as the nature of interaction between amyloid and microglia remain poorly understood. We previously reported a close morphological association between activated microglia and congophilic amyloid plaques in the brains of APP23 transgenic mice at both the light and electron microscopic levels [25]. In the present study, we have further examined the structural relationship between microglia and amyloid deposits by using postembedding immunogold labeling, serial ultrathin sectioning, and 3-dimensional reconstruction. Although bundles of immunogold-labeled amyloid fibrils were completely engulfed by microglial cytoplasm on single sections, serial ultrathin sectioning and three-dimensional reconstruction revealed that these amyloid fibrils are connected to extracellular amyloid deposits. These data demonstrate that extracellular amyloid fibrils form a myriad of finger-like channels with the widely branched microglial cytoplasm. We conclude that in APP23 mice a role of microglia in amyloid phagocytosis and intracellular production of amyloid is unlikely.
Keywords :
Alzheimer’s Disease , Microglia , transgenic mice , Neurodegeneration , brain , aging , CNS , 3-dimensional reconstruction , electronmicroscopy , amyloid
Journal title :
Neurobiology of Aging
Serial Year :
2001
Journal title :
Neurobiology of Aging
Record number :
820048
Link To Document :
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