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Microglia kill amyloid-β1-42 damaged neurons by a CD14-dependent process
被引:35
作者:
Bate, C
Veerhuis, R
Eikelenboom, P
Williarns, A
机构:
[1] Univ Glasgow, Sch Vet, Dept Vet Pathol, Inst Comparat Med, Glasgow G61 1QH, Lanark, Scotland
[2] Vrije Univ Amsterdam, Med Ctr, Neurosci Res Inst, Grad Sch Neurosci Amsterdam,Dept Pathol, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Neurosci Res Inst, Grad Sch Neurosci Amsterdam,Dept Psychiat, Amsterdam, Netherlands
[4] Univ London Royal Vet Coll, Dept Pathol & Infect Dis, N Mymms AL9 7TA, Herts, England
来源:
关键词:
Alzheimer's disease;
amyloid-beta;
CD14;
microglia;
neurotoxicity;
D O I:
10.1097/01.wnr.0000132203.76836.16
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Activated microglia are closely associated with neuronal damage in Alzheimer's disease. In the present study, neurons exposed to low concentrations of amyloid-beta(1-42), a toxic fragment of the amyloid-beta protein, were killed by microglia in a process that required cell-cell contact. Pre-treating microglia with polyclonal antibodies to the CD14 protein, or treating neurons exposed to amyloid-beta(1-42) with a CD14-IgG chimera, prevented the killing of amyloid-beta(1-42) damaged neurons by microglia. Moreover, microglia from CD14 null mice failed to kill amyloid-beta(1-42) damaged neurons. Increased neuronal survival was accompanied by a significant reduction in the production of interleukin-6 indicative of reduced microglial activation. These results indicate an important role for CD14 in the recognition and subsequent killing of amyloid-beta damaged neurons by microglia.
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页码:1427 / 1430
页数:4
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