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

作者：Qian Feng^*; Deng Jing; Gantner Benjamin N; Flavell Richard A; Dong Chen; Christman John W; Ye Richard D

来源：American Journal of Physiology - Lung Cellular and Molecular Physiology, 2012, 302(9): L866-L874.

DOI：10.1152/ajplung.00277.2011

• lung inflammation
• macrophages
• cytokines

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.

• 出版日期2012-5