A cell biological view of Toll-like receptor function: regulation through compartmentalization

被引:518
作者
Barton, Gregory M. [1 ]
Kagan, Jonathan C. [2 ,3 ]
机构
[1] Univ Calif Berkeley, Div Immunol & Pathogenesis, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Childrens Hosp, Div Gastroenterol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
ACTIVATE B-CELLS; NF-KAPPA-B; ADAPTER MOLECULE; SIGNALING PATHWAY; INTERFERON-BETA; CRYSTAL-STRUCTURE; DENDRITIC CELLS; SPLICE VARIANT; MURINE LUPUS; SELF-DNA;
D O I
10.1038/nri2587
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An emerging paradigm in innate immune signalling is that cell biological context can influence the outcome of a ligand-receptor interaction. In this Review we discuss how Toll-like receptor (TLR) activation and signal transduction are regulated by subcellular compartmentalization of receptors and downstream signalling components. In particular, we focus on the functional specialization of TLRs in the endosomal system. We discuss recent studies that illustrate how basic aspects of the cellular machinery contribute to TLR function and regulation. This emerging area of research will provide important information on how immune signal transduction networks depend on (and in some cases influence) the generic regulators that organize eukaryotic cells.
引用
收藏
页码:535 / 542
页数:8
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