Targeting innate immunity protein kinase signalling in inflammation

被引:296
作者
Gaestel, Matthias [1 ]
Kotlyarov, Alexey [1 ]
Kracht, Michael [2 ]
机构
[1] Hannover Med Sch, Inst Biochem, D-30625 Hannover, Germany
[2] Univ Giessen, Rudolf Buchheim Inst Pharmacol, D-35392 Giessen, Germany
关键词
NF-KAPPA-B; TUMOR-NECROSIS-FACTOR; COLLAGEN-INDUCED ARTHRITIS; P38-ALPHA MAP KINASE; EMBRYONIC CARDIOVASCULAR DEVELOPMENT; ACTIVATED PROTEIN-KINASE-2 MK-2; VIVO ANTIINFLAMMATORY ACTIVITY; JUN NH2-TERMINAL KINASE-1; SMALL-MOLECULE INHIBITOR; BRUTONS TYROSINE KINASE;
D O I
10.1038/nrd2829
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Inflammation is an evolutionarily conserved host reaction that is initiated in response to trauma, tissue damage and infection. It leads to changes in tissue homeostasis and blood flow, immune-cell activation and migration, and secretion of cytokines and mediators in a spatio-temporally coordinated manner. Progress in understanding of the mechanisms of the inflammatory response has identified various protein kinases that act as essential signalling components and therefore represent potential therapeutic targets. This article summarizes advances in the identification and validation of such targets, and discusses key issues for the development of small-molecule kinase inhibitors as a new generation of oral anti-inflammatory drugs, including feedback loops, inhibitor specificity and combination therapy.
引用
收藏
页码:480 / 499
页数:20
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