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表皮生长因子诱导的快速而持续的核细胞质 ERK 振荡。

Rapid and sustained nuclear-cytoplasmic ERK oscillations induced by epidermal growth factor.

机构信息

Systems Biology Program, Pacific Northwest National Laboratory, Richland, WA, USA.

出版信息

Mol Syst Biol. 2009;5:332. doi: 10.1038/msb.2009.90. Epub 2009 Dec 1.

Abstract

Although the ERK pathway has a central role in the response of cells to growth factors, its regulatory structure and dynamics are incompletely understood. To investigate ERK activation in real time, we expressed an ERK-GFP fusion protein in human mammary epithelial cells. On EGF stimulation, we observed sustained oscillations of the ERK-GFP fusion protein between the nucleus and cytoplasm with a periodicity of approximately 15 min. The oscillations were persistent (>45 cycles), independent of cell cycle phase, and were highly dependent on cell density, essentially disappearing at confluency. Oscillations occurred even at ligand doses that elicited very low levels of ERK phosphorylation, and could be detected biochemically in both transfected and nontransfected cells. Mathematical modeling revealed that negative feedback from phosphorylated ERK to the cascade input was necessary to match the robustness of the oscillation characteristics observed over a broad range of ligand concentrations. Our characterization of single-cell ERK dynamics provides a quantitative foundation for understanding the regulatory structure of this signaling cascade.

摘要

尽管 ERK 通路在细胞对生长因子的反应中起着核心作用,但它的调节结构和动力学仍不完全清楚。为了实时研究 ERK 的激活,我们在人乳腺上皮细胞中表达了一种 ERK-GFP 融合蛋白。在 EGF 刺激下,我们观察到 ERK-GFP 融合蛋白在细胞核和细胞质之间持续振荡,其周期性约为 15 分钟。这些振荡是持久的(>45 个周期),与细胞周期阶段无关,并且高度依赖于细胞密度,在细胞汇合时几乎消失。即使在引发 ERK 磷酸化水平非常低的配体剂量下,也可以观察到振荡,并且可以在转染和未转染的细胞中通过生化方法检测到。数学模型表明,磷酸化 ERK 对级联输入的负反馈对于匹配在广泛的配体浓度范围内观察到的振荡特征的稳健性是必要的。我们对单个细胞 ERK 动力学的表征为理解该信号级联的调节结构提供了定量基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e57/2824491/b2d2e3ff6538/msb200990-f1.jpg

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