期刊
JOURNAL OF NEURAL TRANSMISSION
卷 116, 期 11, 页码 1427-1434出版社
SPRINGER WIEN
DOI: 10.1007/s00702-009-0218-9
关键词
Apolipoprotein E4; Beta amyloid (A beta); Brain inflammation; CA1 septal neurons; Microglia; Astrocytes; Neprilysin; Neurodegeneration
Apolipoprotein E4 (ApoE4), the most prevalent genetic risk factor for Alzheimer's disease, is histopathologically associated with increased deposition of amyloid-beta and brain inflammation and with impaired neuronal plasticity and repair. We have recently shown that the activation of the amyloid cascade by inhibition of the A beta-degrading enzyme, neprilysin, stimulates the isoform-specific degeneration of hippocampal CA1 neurons and septal neurons in apoE4 transgenic mice and that this effect is accompanied by the accumulation of intracellular A beta in the affected neurons. We presently examined the extent to which this apoE4-dependent A beta-mediated neurodegeneration is associated with brain area specific inflammatory activation. This revealed that the activation of the amyloid cascade in apoE transgenic mice results in the activation of microgliosis and astrogliosis in the hippocampus of apoE4, but not in apoE3 transgenic mice. The effect was most pronounced in the hippocampal CA1 subfield and its initial kinetics followed that of the accumulation of A beta in CA1 neurons. In contrast, the corresponding apoE4-dependent A beta degeneration of septal neurons was not associated with the activation of either gliosis or astrogliosis in this brain area. These animal model findings, that the association between brain inflammation and neurodegeneration is brain area specific, suggest that neuropathological inflammatory interactions in AD may also be brain area specific and that consequently the efficacy of putative anti-inflammatory intervention may also be brain area selective.
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