TLR5型
TLR2型
TLR4型
葡聚糖
Toll样受体
免疫系统
化学
受体
细胞因子
微生物学
生物化学
生物
先天免疫系统
免疫学
作者
Pochanart Kanjan,Neha M. Sahasrabudhe,Bart J. de Haan,Paul de Vos
标识
DOI:10.1016/j.jff.2017.07.061
摘要
Particulate β-glucans enhanced NF-κB expression in cell-lines co-expressing Dectin-1A-TLR4 and Dectin-1B-TLR4, while soluble β-glucans only synergistically acted on Dectin-1A-TLR4. This was different with Dectin-1 co-expressing TLR2 and TLR5, which inhibited activation after particulate and soluble β-glucan stimulation. The co-acting effect of extracellular TLR2, TLR4 and TLR5 and Dectin-1 by particulate and soluble β-glucan on cytokine production was confirmed in THP-1 macrophages. Dectin-1 activation by particulate β-glucans during TLR2 and TLR4 but not TLR5 blocking was shown to enhance the pro-inflammatory cytokines IL-6, IL-8 and TNF-α in THP-1 macrophages. This effect was stronger with particulate than with soluble β-glucan. The data demonstrate that β-glucans is an immune regulatory ligand for TLR2 and TLR4.
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