Microglia kill amyloid-beta1-42 damaged neurons by a CD14-dependent process

Clive Bate, Robert Veerhuis, Piet Eikelenboom, Alun Williams

Research output: Contribution to journalArticleAcademicpeer-review

38 Citations (Scopus)

Abstract

Activated microglia are closely associated with neuronal damage in Alzheimer's disease. In the present study, neurons exposed to low concentrations of amyloid-beta1-42, 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-beta1-42 with a CD14-IgG chimera, prevented the killing of amyloid-beta1-42 damaged neurons by microglia. Moreover, microglia from CD14 null mice failed to kill amyloid-beta1-42 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
Original languageEnglish
Pages (from-to)1427-1430
JournalNeuroReport
Volume15
Issue number9
DOIs
Publication statusPublished - 2004

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