先天免疫系统
细胞生物学
获得性免疫系统
生物
信号转导
脂筏
免疫系统
T细胞
调节器
ZAP70型
先天性淋巴细胞
T细胞受体
免疫学
生物化学
基因
作者
Nobutaka Suzuki,Shinobu Suzuki,Douglas G. Millar,Midori Unno,Hiromitsu Hara,Thomas Calzascia,Sho Yamasaki,Tadashi Yokosuka,Nien‐Jung Chen,Alisha R. Elford,Jun-ichiro Suzuki,Arata Takeuchi,Christine Mirtsos,Denis Bouchard,Pamela S. Ohashi,Wen‐Chen Yeh,Takashi Saito
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2006-03-30
卷期号:311 (5769): 1927-1932
被引量:111
标识
DOI:10.1126/science.1124256
摘要
IRAK-4 is a protein kinase that is pivotal in mediating signals for innate immune responses. Here, we report that IRAK-4 signaling is also essential for eliciting adaptive immune responses. Thus, in the absence of IRAK-4, in vivo T cell responses were significantly impaired. Upon T cell receptor stimulation, IRAK-4 is recruited to T cell lipid rafts, where it induces downstream signals, including protein kinase C activation through the association with Zap70. This signaling pathway was found to be required for optimal activation of nuclear factor kappaB. Our findings suggest that T cells use this critical regulator of innate immunity for the development of acquired immunity, suggesting that IRAK-4 may be involved in direct signal cross talk between the two systems.
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