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The frequencies of calcium oscillations are optimized for efficient calcium-mediated activation of Ras and the ERK/MAPK cascade

机译:钙振荡频率经过优化,可有效地通过钙介导的Ras和ERK / MAPK级联反应激活

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摘要

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+)]_i) can modulate Ras activation. Increases in [Ca~(2+)]_i 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/MARK signaling cascade.
机译:Ras蛋白是二元开关,通过循环通过无效的GDP结合和活性的GTP结合构象,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,已知受体介导的细胞内游离钙([Ca〜(2 +)] _ i)浓度增加可以调节Ras活化。 [Ca〜(2 +)] _ i的增加通常是重复出现的Ca〜(2+)尖峰或振荡。这些重复的Ca〜(2+)振荡是由电刺激或受体刺激引起的,其频率随受体刺激幅度的增加而增加,这对诱导选择性细胞功能至关重要。在这里,我们表明,Ca〜(2+)振荡是针对Ca〜(2+)介导的Ras激活和通过细胞外信号调节激酶(ERK)丝裂原激活的蛋白激酶(MAPK)级联信号传递而优化的。我们提供了另外的证据,即Ca〜(2+)振荡降低了激活Ras的有效Ca〜(2+)阈值,并且振荡频率针对Ras和ERK / MAPK通路的激活进行了优化。我们的结果描述了迄今为止未知的复杂Ca〜(2+)信号与Ras / ERK / MARK信号级联的调制之间的联系。

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