MAP Kinase Phosphatase-1 and Septic Shock.

Yusen Liu, Thomas P Shanley
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Abstract

Mitogen-activated protein (MAP)(§) kinase cascades are crucial signal transduction pathways in the biosynthesis of proinflammatory cytokines. MAP kinase phosphatase (MKP)-1, an archetypal member of the MKP family, plays a pivotal role in the feedback control of p38 and JNK. In vitro studies using cultured macrophages have provided strong evidence for a critical role of MKP-1 in the restraint of pro-inflammatory cytokine biosynthesis. Recently, a number of studies conducted using MKP-1 knockout mice have verified the importance of MKP-1 in the regulation of p38 and JNK and in the regulation of pro-inflammatory cytokine synthesis. Upon lipopolysaccharide challenge MKP-1 knockout mice produced dramatically greater amounts of inflammatory cytokines, developed severe hypotension, and multi-organ failure, and exhibited a remarkable increase in mortality. These studies demonstrate that MKP-1 is an essential feedback regulator of the innate immune response, and that it plays a critical role in preventing septic shock and multi-organ dysfunction during pathogenic infection.

MAP激酶磷酸酶-1与感染性休克。
丝裂原活化蛋白(MAP)激酶级联是促炎细胞因子生物合成的重要信号转导途径。MAP激酶磷酸酶(MKP)-1是MKP家族的原型成员,在p38和JNK的反馈控制中起关键作用。利用培养的巨噬细胞进行的体外研究提供了强有力的证据,证明MKP-1在抑制促炎细胞因子的生物合成中起着关键作用。最近,许多使用MKP-1敲除小鼠进行的研究证实了MKP-1在调节p38和JNK以及调节促炎细胞因子合成中的重要性。在脂多糖刺激下,MKP-1基因敲除小鼠产生了大量的炎症细胞因子,出现了严重的低血压和多器官衰竭,并表现出死亡率的显著增加。这些研究表明,MKP-1是先天免疫应答的重要反馈调节因子,在病原性感染中预防感染性休克和多器官功能障碍中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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