Cutting edge: The immunostimulatory activity of the lung surfactant protein-A involves toll-like receptor 4

被引:246
作者
Guillot, L
Balloy, V
McCormack, FX
Golenbock, DT
Chignard, M
Si-Tahar, M
机构
[1] Inst Pasteur, Unite Def Innee & Inflammat, INSERM, U485, F-75015 Paris, France
[2] Univ Cincinnati, Dept Med, Div Pulm & Crit Care Med, Cincinnati, OH 45267 USA
[3] Univ Massachusetts, Sch Med, Dept Med, Div Infect Dis, Worcester, MA 01655 USA
关键词
D O I
10.4049/jimmunol.168.12.5989
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The collectin surfactant protein-A (SP-A) is involved in the innate host defense and the regulation of inflammatory processes in the lung. In this work we investigated the molecular mechanisms related to the immunostimulatory activity of SP-A using macrophages from C3H/HeJ mice, which carry an inactivating mutation in the Toll-like receptor (TLR)4 gene, and TLR4-transfected Chinese. hamster ovary cells. We demonstrate that SP-A-induced activation of the NF-kappaB signaling pathway and up-regulation of cytokine synthesis such as TNF-alpha and IL-10 are critically dependent on the TLR4 functional complex. These findings support the concept that TLR4 is a pattern recognition receptor that signals in response to both foreign pathogens and endogenous host mediators.
引用
收藏
页码:5989 / 5992
页数:4
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