Syk-dependent ERK activation regulates IL-2 and IL-10 production by DC stimulated with zymosan

被引:134
作者
Slack, Emma C.
Robinson, Matthew J.
Hernanz-Falcon, Patricia
Brown, Gordon D.
Williams, David L.
Schweighoffer, Edina
Tybulewicz, Victor L.
Reis e Sousa, Caetano
机构
[1] London Res Inst, Immunobiol Lab, Canc Res UK, London WC2A 3PX, England
[2] Univ Cape Town, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa
[3] E Tennessee State Univ, James H Quillen Coll Med, Dept Surg, Johnson City, TN 37614 USA
[4] Natl Inst Med Res, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
C-type lectins; dendritic cells; pattern recognition receptors; Syk; zymosan;
D O I
10.1002/eji.200636830
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Zymosan is a particulate yeast preparation that elicits high levels of IL-2 and IL-10 from dendritic cells (DC) and engages multiple innate receptors, including the Syk-coupled receptor dectin-1 and the MyD88-coupled receptor TLR2. Here, we show that induction of IL-2 and IL-10 by zymosan requires activation of ERK MAP kinase in murine DC. Surprisingly, ERK activation in response to zymosan is completely blocked in Sykdeficient DC and unaffected by MyD88 deficiency. Conversely, ERK activation in response to the TLR2 agonist Pam3Cys is completely MyD88 dependent and unaffected by Syk deficiency. The inability of TLR2 ligands in zymosan to couple to ERK may explain the Syk dependence of the IL-2 and IL-10 response in DC and emphasises the importance of Syk-coupled pattern recognition receptors such as dectin-1 in the detection of yeasts. Furthermore, the lack of receptor compensation observed here suggests that responses induced by complex innate stimuli cannot always be predicted by the signalling pathways downstream of individual receptors.
引用
收藏
页码:1600 / 1612
页数:13
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