Map kinase phosphatase 5 protects against sepsis-induced acute lung injury

被引:48
|
作者
Qian, Feng [1 ]
Deng, Jing [2 ,3 ]
Gantner, Benjamin N. [1 ]
Flavell, Richard A. [4 ,5 ]
Dong, Chen [6 ]
Christman, John W. [3 ]
Ye, Richard D. [1 ]
机构
[1] Univ Illinois Med, Dept Pharmacol, Chicago, IL 60612 USA
[2] Univ Illinois Med, Dept Physiol & Biophys, Chicago, IL 60612 USA
[3] Univ Illinois Med, Dept Med, Chicago, IL 60612 USA
[4] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[5] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
lung inflammation; macrophages; cytokines; TOLL-LIKE RECEPTOR; NF-KAPPA-B; IMMUNE-RESPONSES; NITRIC-OXIDE; INFLAMMATORY RESPONSES; MACROPHAGE ACTIVATION; CYTOKINE BIOSYNTHESIS; ALVEOLAR MACROPHAGES; MESSENGER-RNA; LPS;
D O I
10.1152/ajplung.00277.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Qian F, Deng J, Gantner BN, Flavell RA, Dong C, Christman JW, Ye RD. Map kinase phosphatase 5 protects against sepsis-induced acute lung injury. Am J Physiol Lung Cell Mol Physiol 302: L866-L874, 2012. First published February 3, 2012; doi: 10.1152/ajplung.00277.2011.-Mitogen-activated protein kinases (MAPKs) play a critical role in inflammation. Although activation of MAPK in inflammatory cells has been studied extensively, much less is known about the inactivation of these kinases. MAPK phosphatase 5 (MKP5) is a member of the dual-specificity phosphatase family that dephosphorylates activated MAPKs. Here we report that MKP5 protects sepsis-induced acute lung injury. Mice lacking MKP5 displayed severe lung tissue damage following LPS challenge, characterized with increased neutrophil infiltration and edema compared with wild-type (WT) controls. In response to LPS, MKP5-deficient macrophages produced significantly more inflammatory factors including inflammatory cytokines, nitric oxide, and superoxide. Phosphorylation of p38 MAPK, JNK, and ERK were enhanced in MKP5-deficient macrophages upon LPS stimulation. Adoptive transfer of MKP5-deficient macrophages led to more severe lung inflammation than transfer of WT macrophages, suggesting that MKP5-deficient macrophages directly contribute to acute lung injury. Taken together, these results suggest that MKP5 is crucial to homeostatic regulation of MAPK activation in inflammatory responses.
引用
收藏
页码:L866 / L874
页数:9
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