Son Yong, Kim Sangduck, Chung Hun-Taeg, Pae Hyun-Ock
Department of Anesthesiology and Pain Medicine, Wonkwang University School of Medicine, Iksan, Republic of Korea.
Methods Enzymol. 2013;528:27-48. doi: 10.1016/B978-0-12-405881-1.00002-1.
There are three well-defined subgroups of mitogen-activated protein kinases (MAPKs): the extracellular signal-regulated kinases (ERKs), the c-Jun N-terminal kinases (JNKs), and the p38 MAPKs. Three subgroups of MAPKs are involved in both cell growth and cell death, and the tight regulation of these pathways, therefore, is paramount in determining cell fate. MAPK pathways have been shown to be activated not only by receptor ligand interactions but also by different stressors placed on the cell. MAPK phosphatases (MKPs) dephosphorylate and deactivate MAPKs. Reactive oxygen species (ROS), such as hydrogen peroxide, have been reported to activate ERKs, JNKs, and p38 MAPKs, but the mechanisms by which ROS can activate these kinases are unclear. Oxidative modifications of MAPK signaling proteins and inactivation and/or degradation of MKPs may provide the plausible mechanisms for activation of MAPK pathways by ROS, which will be reviewed in this chapter.
有丝分裂原活化蛋白激酶(MAPK)有三个明确的亚组:细胞外信号调节激酶(ERK)、c-Jun氨基末端激酶(JNK)和p38 MAPK。MAPK的三个亚组都参与细胞生长和细胞死亡,因此,这些信号通路的严格调控对于决定细胞命运至关重要。已表明MAPK信号通路不仅可通过受体配体相互作用激活,还可被施加于细胞的不同应激源激活。MAPK磷酸酶(MKP)使MAPK去磷酸化并使其失活。据报道,活性氧(ROS),如过氧化氢,可激活ERK、JNK和p38 MAPK,但ROS激活这些激酶的机制尚不清楚。MAPK信号蛋白的氧化修饰以及MKP的失活和/或降解可能为ROS激活MAPK信号通路提供合理机制,本章将对此进行综述。