Plevin R, Scott P H, Robinson C J, Gould G W
Department of Physiology and Pharmacology, University of Strathclyde, Glasgow, U.K.
Biochem J. 1996 Sep 1;318 ( Pt 2)(Pt 2):657-63. doi: 10.1042/bj3180657.
In rat aortic smooth muscle cells, platelet-derived growth factor (PDGF) stimulated a sustained activation of mitogen-activated protein kinase (MAP kinase) while the response to angiotensin II (AII) was transient. This was due to a relatively greater initial activation of MAP kinase kinase (MEK) and a correspondingly greater residual MEK activity at later time points. Pretreatment of cells with the novel MEK inhibitor PD 098059 reduced MEK activation at 5 min in response to each agonist by a similar proportion (70%); however, at this time point MAP kinase activation in response to PDGF was only marginally affected while the response to AII was substantially reduced. PD 098059 did, however, reduce PDGF-stimulated MEK activity after 30 min and this correlated with a loss in MAP kinase activity and DNA synthesis. Pretreatment with forskolin also caused a similar pattern of inhibition of agonist-stimulated MEK and MAP kinase activity. Only following protein kinase C down-regulation were both AII- and PDGF-stimulated MAP kinase activation substantially reduced and this correlated with the virtual loss of both MEK and c-Raf-1 activity in response to both agents. The differential inhibition of MAP kinase activation by forskolin was not due to specific activation of A-Raf by PDGF; both PDGF and AII stimulated A-Raf kinase and this activity was strongly inhibited by forskolin. These results suggest that the efficacy of MEK activation determines the duration of MAP kinase activation and the susceptibility of MAP kinase activation to inhibition by different agents. The results also argue against the selective activation of A-Raf by PDGF as a mechanism to explain the differences in the kinetics of MAP kinase activity stimulated by AII and PDGF.
在大鼠主动脉平滑肌细胞中,血小板衍生生长因子(PDGF)可刺激丝裂原活化蛋白激酶(MAP激酶)持续激活,而对血管紧张素II(AII)的反应则是短暂的。这是由于MAP激酶激酶(MEK)相对更大程度的初始激活以及在随后时间点相应更大的残余MEK活性所致。用新型MEK抑制剂PD 098059预处理细胞,可使在5分钟时对每种激动剂的MEK激活以相似比例(70%)降低;然而,在此时间点,对PDGF的MAP激酶激活仅受到轻微影响,而对AII的反应则大幅降低。不过,PD 098059在30分钟后确实降低了PDGF刺激的MEK活性,这与MAP激酶活性和DNA合成的丧失相关。用福司可林预处理也导致了类似的对激动剂刺激的MEK和MAP激酶活性的抑制模式。仅在蛋白激酶C下调后,AII和PDGF刺激的MAP激酶激活才大幅降低,这与对两种试剂反应中MEK和c-Raf-1活性的几乎丧失相关。福司可林对MAP激酶激活的差异抑制并非由于PDGF对A-Raf的特异性激活;PDGF和AII均刺激A-Raf激酶,且该活性被福司可林强烈抑制。这些结果表明,MEK激活的效力决定了MAP激酶激活的持续时间以及MAP激酶激活对不同试剂抑制的敏感性。结果还反对将PDGF对A-Raf的选择性激活作为解释AII和PDGF刺激的MAP激酶活性动力学差异的机制。