Zhang S, Han J, Sells M A, Chernoff J, Knaus U G, Ulevitch R J, Bokoch G M
Department of Immunology, Scripps Research Institute, La Jolla, California 92037, USA.
J Biol Chem. 1995 Oct 13;270(41):23934-6. doi: 10.1074/jbc.270.41.23934.
The stress-activated p38 mitogen-activated protein (MAP) kinase defines a subgroup of the mammalian MAP kinases that appear to play a key role in regulating inflammatory responses. Co-expression of constitutively active forms of Rac and Cdc42 leads to activation of p38 while dominant negative Rac and Cdc42 inhibit the ability of interleukin-1 to increase p38 activity. p21-activated kinase 1 (Pak1) is a potential mediator of Rac/Cdc42 signaling, and we observe that Pak1 stimulates p38 activity. A dominant negative Pak1 suppresses both interleukin-1- and Rac/Cdc42-induced p38 activity. Rac and Cdc42 appear to regulate a protein kinase cascade initiated at the level of Pak and leading to activation of p38 and JNK.
应激激活的p38丝裂原活化蛋白(MAP)激酶是哺乳动物MAP激酶的一个亚组,似乎在调节炎症反应中起关键作用。组成型活性形式的Rac和Cdc42共表达导致p38激活,而显性负性Rac和Cdc42抑制白细胞介素-1增加p38活性的能力。p21激活激酶1(Pak1)是Rac/Cdc42信号传导的潜在介质,我们观察到Pak1刺激p38活性。显性负性Pak1抑制白细胞介素-1和Rac/Cdc42诱导的p38活性。Rac和Cdc42似乎调节一个蛋白激酶级联反应,该反应始于Pak水平并导致p38和JNK激活。