Kupzig Sabine, Walker Simon A, Cullen Peter J
Henry Wellcome Integrated Signalling Laboratories, Department of Biochemistry, School of Medical Sciences, University of Bristol, Bristol BS8 1TD, UK.
Proc Natl Acad Sci U S A. 2005 May 24;102(21):7577-82. doi: 10.1073/pnas.0409611102. Epub 2005 May 12.
Ras proteins are binary switches that, by cycling through inactive GDP- and active GTP-bound conformations, regulate multiple cellular signaling pathways, including those that control growth and differentiation. For some time, it has been known that receptor-mediated increases in the concentration of intracellular free calcium (Ca(2+)) can modulate Ras activation. Increases in Ca(2+) often occur as repetitive Ca(2+) spikes or oscillations. Induced by electrical or receptor stimuli, these repetitive Ca(2+) oscillations increase in frequency with the amplitude of receptor stimuli, a phenomenon critical for the induction of selective cellular functions. Here, we show that Ca(2+) oscillations are optimized for Ca(2+)-mediated activation of Ras and signaling through the extracellular signal-regulated kinase (ERK)/mitogen-activated protein kinase (MAPK) cascade. We present additional evidence that Ca(2+) oscillations reduce the effective Ca(2+) threshold for the activation of Ras and that the oscillatory frequency is optimized for activation of Ras and the ERK/MAPK pathway. Our results describe a hitherto unrecognized link between complex Ca(2+) signals and the modulation of the Ras/ERK/MAPK signaling cascade.
Ras蛋白是二元开关,通过在无活性的GDP结合构象和活性的GTP结合构象之间循环,调节多种细胞信号通路,包括控制生长和分化的信号通路。一段时间以来,人们已经知道受体介导的细胞内游离钙([Ca(2+)]i)浓度增加可调节Ras激活。[Ca(2+)]i的增加通常表现为重复性的Ca(2+)尖峰或振荡。由电刺激或受体刺激诱导,这些重复性的Ca(2+)振荡频率随受体刺激幅度增加,这一现象对于诱导选择性细胞功能至关重要。在这里,我们表明Ca(2+)振荡针对Ca(2+)介导的Ras激活以及通过细胞外信号调节激酶(ERK)/丝裂原活化蛋白激酶(MAPK)级联的信号传导进行了优化。我们提供了额外的证据,表明Ca(2+)振荡降低了Ras激活的有效Ca(2+)阈值,并且振荡频率针对Ras和ERK/MAPK途径的激活进行了优化。我们的结果描述了复杂的Ca(2+)信号与Ras/ERK/MAPK信号级联调节之间迄今为止未被认识的联系。