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单个细胞中的Akt信号动力学。

Akt signaling dynamics in individual cells.

作者信息

Gross Sean M, Rotwein Peter

机构信息

Department of Biochemistry and Molecular Biology, Oregon Health & Science University, Portland, OR 97239, USA.

Department of Biochemistry and Molecular Biology, Oregon Health & Science University, Portland, OR 97239, USA Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech Health University Health Sciences Center, El Paso, TX 79905, USA

出版信息

J Cell Sci. 2015 Jul 15;128(14):2509-19. doi: 10.1242/jcs.168773. Epub 2015 Jun 3.

Abstract

The protein kinase Akt (for which there are three isoforms) is a key intracellular mediator of many biological processes, yet knowledge of Akt signaling dynamics is limited. Here, we have constructed a fluorescent reporter molecule in a lentiviral delivery system to assess Akt kinase activity at the single cell level. The reporter, a fusion between a modified FoxO1 transcription factor and clover, a green fluorescent protein, rapidly translocates from the nucleus to the cytoplasm in response to Akt stimulation. Because of its long half-life and the intensity of clover fluorescence, the sensor provides a robust readout that can be tracked for days under a range of biological conditions. Using this reporter, we find that stimulation of Akt activity by IGF-I is encoded into stable and reproducible analog responses at the population level, but that single cell signaling outcomes are variable. This reporter, which provides a simple and dynamic measure of Akt activity, should be compatible with many cell types and experimental platforms, and thus opens the door to new insights into how Akt regulates its biological responses.

摘要

蛋白激酶Akt(有三种亚型)是许多生物过程的关键细胞内介质,但对Akt信号动力学的了解有限。在这里,我们在慢病毒递送系统中构建了一种荧光报告分子,以在单细胞水平评估Akt激酶活性。该报告分子是一种修饰的FoxO1转录因子与绿色荧光蛋白三叶草的融合体,响应Akt刺激时会迅速从细胞核转运到细胞质中。由于其三叶草荧光的长半衰期和强度,该传感器提供了一种强大的读数,可在一系列生物学条件下追踪数天。使用该报告分子,我们发现IGF-I对Akt活性的刺激在群体水平上被编码为稳定且可重复的类似反应,但单细胞信号结果是可变的。这种报告分子提供了一种简单而动态的Akt活性测量方法,应该与许多细胞类型和实验平台兼容,从而为深入了解Akt如何调节其生物学反应打开了大门。

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