首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Receptor Level Mechanisms Are Required for Epidermal Growth Factor (EGF)-stimulated Extracellular Signal-regulated Kinase (ERK) Activity Pulses
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Receptor Level Mechanisms Are Required for Epidermal Growth Factor (EGF)-stimulated Extracellular Signal-regulated Kinase (ERK) Activity Pulses

机译:表皮生长因子(EGF)刺激的细胞外信号调节激酶(ERK)活动脉冲需要受体水平的机制

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摘要

In both physiological and cell culture systems, EGF-stimulated ERK activity occurs in discrete pulses within individual cells. Many feedback loops are present in the EGF receptor (EGFR)-ERK network, but the mechanisms driving pulsatile ERK kinetics are unknown. Here, we find that in cells that respond to EGF with frequency-modulated pulsatile ERK activity, stimulation through a heterologous TrkA receptor system results in non-pulsatile, amplitude-modulated activation of ERK. We further dissect the kinetics of pulse activity using a combination of FRET- and translocation-based reporters and find that EGFR activity is required to maintain ERK activity throughout the 10–20-minute lifetime of pulses. Together, these data indicate that feedbacks operating within the core Ras-Raf-MEK-ERK cascade are insufficient to drive discrete pulses of ERK activity and instead implicate mechanisms acting at the level of EGFR.
机译:在生理和细胞培养系统中,EGF刺激的ERK活性都发生在单个细胞内的离散脉冲中。 EGF受体(EGFR)-ERK网络中存在许多反馈回路,但驱动脉动ERK动力学的机制尚不清楚。在这里,我们发现在对具有频率调制的脉动ERK活性的EGF作出反应的细胞中,通过异源TrkA受体系统的刺激会导致ERK的非脉动,幅度调制的激活。我们进一步结合使用基于FRET和易位的报告基因来分析脉冲活动的动力学,发现在整个脉冲寿命10–20分钟内,EGFR活性是维持ERK活性所必需的。总之,这些数据表明,在核心Ras-Raf-MEK-ERK级联内运行的反馈不足以驱动ERK活动的离散脉冲,而是暗示了在EGFR水平起作用的机制。

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