Lipids that directly regulate innate immune signal transduction

被引:29
作者
Barnett, Katherine C. [1 ,2 ]
Kagan, Jonathan C. [1 ,2 ]
机构
[1] Harvard Med Sch, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Div Gastroenterol, Boston, MA 02115 USA
关键词
TLRs; innate immunity; myddosome; localization; phosphoinositides; PRRs; sorting adaptor; SMOC; cGAS; TIRAP; MIXED LINEAGE KINASE; NF-KAPPA-B; PHOSPHOINOSITIDE BINDING; OXIDIZED PHOSPHOLIPIDS; NLRP3; INFLAMMASOME; SUBCELLULAR SITES; PLASMA-MEMBRANE; PROTEIN; ADAPTER; DOMAIN;
D O I
10.1177/1753425919852695
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pattern Recognition Receptors (PRRs) detect evidence of infection and tissue damage. The activation of these receptors and their downstream signal transduction pathways initiate a protective immune response. These signaling pathways are influenced by their spatial context, and precise subcellular positioning of proteins and protein complexes in these pathways is essential for effective immune responses in vivo. This organization is not limited to transmembrane proteins that reside in specific organelles, but also to proteins that engage membrane lipid head groups for proper positioning. In this review, we focus on the role of cell membranes and protein-lipid interactions in innate immune signal transduction and how their mechanisms of localization regulate the immune response. We will discuss how lipids spatially regulate the sensing of damage or infection, mediate effector activity, and serve as messengers of cell death and tissue damage.
引用
收藏
页码:4 / 14
页数:11
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