作者: Sonia Franciosi , Hyun B. Choi , Seung U. Kim , James G. McLarnon
DOI: 10.1016/J.JNEUROIM.2004.10.006
关键词: Immunocytochemistry 、 Interleukin 8 、 Microglia 、 Stimulation 、 Chemistry 、 Endocrinology 、 Amyloid beta 、 Cytokine 、 Chemokine 、 Proinflammatory cytokine 、 Internal medicine
摘要: Abstract The effects of the chemokine IL-8 on amyloid beta peptide (Aβ1-42)-induced responses in cultured human microglia were investigated using RT–PCR, ELISA and immunocytochemistry. Aβ1-42 (5 μM) applied for 8 h induced expression increased production pro-inflammatory cytokines IL-6, IL-1β, TNF-α, inducible enzyme COX-2 IL-8. Microglial treatment with added (at 100 ng/mL) led to enhancement both all these factors compared alone. Stimulation itself was effective increasing microglial cytokines, COX-2, however, had no effect protein levels factors. anti-inflammatory IL-10 TGFβ1 remained unchanged from basal stimulation either Aβ1-42, or together actions potentiate Aβ1-42-induced inflammatory mediators may have particular relevance Alzheimer disease brain which exhibits elevated chemokine.