Kalmes A, Deou J, Clowes A W, Daum G
Department of Surgery, University of Washington, Seattle 98195-6410, USA.
FEBS Lett. 1999 Feb 5;444(1):71-4. doi: 10.1016/s0014-5793(99)00034-4.
SB203580 (4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)1H-imi dazole) is widely used as a specific inhibitor of p38 mitogen-activated protein kinase (MAPK). Here, we report that SB203580 activates the serine/threonine kinase Raf-1 in quiescent smooth muscle cells in a dose-dependent fashion. The concentrations of SB203580 required lie above those necessary to inhibit p38 MAPK and we were unable to detect basal levels of active p38 MAPK. SB203580 does not directly activate Raf-1 in vitro, and fails to activate Ras, MEK, and ERK in intact cells. In vitro, however, SB203580-stimulated Raf-1 activates MEK1 in a coupled assay. We conclude that activation of Raf-1 by SB203580 is not mediated by an inhibition of p38 MAPK, is Ras-independent, and is uncoupled from MEK/ERK signaling.
SB203580(4-(4-氟苯基)-2-(4-甲亚磺酰基苯基)-5-(4-吡啶基)-1H-咪唑)被广泛用作p38丝裂原活化蛋白激酶(MAPK)的特异性抑制剂。在此,我们报告SB203580以剂量依赖方式激活静止平滑肌细胞中的丝氨酸/苏氨酸激酶Raf-1。所需的SB203580浓度高于抑制p38 MAPK所需的浓度,并且我们无法检测到活性p38 MAPK的基础水平。SB203580在体外不直接激活Raf-1,并且在完整细胞中不能激活Ras、MEK和ERK。然而,在体外,SB203580刺激的Raf-1在偶联测定中激活MEK1。我们得出结论,SB203580对Raf-1的激活不是由p38 MAPK的抑制介导的,不依赖于Ras,并且与MEK/ERK信号传导解偶联。