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Variability in G-Protein-Coupled Signaling Studied with Microfluidic Devices

机译:用微流体装置研究G蛋白偶联信号的变异性

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摘要

Different cells, even those that are genetically identical, can respond differently to identical stimuli, but the precise source of this variability remains obscure. To study this problem, we built a microfluidic experimental system which can track responses of individual cells across multiple stimulations. We used this system to determine that amplitude variation in G-protein-activated calcium release in RAW264.7 macrophages is generally extrinsic, i.e., they arise from long-lived variations between cells and not from stochastic activation of signaling components. In the case of responses linked to P2Y family purine receptors, we estimate that approximately one-third of the observed variability in calcium release is receptor-specific. We further demonstrate that the signaling apparatus downstream of P2Y6 receptor activation is moderately saturable. These observations will be useful in constructing and constraining single-cell models of G protein-coupled calcium dynamics.
机译:不同的细胞,即使是遗传上相同的细胞,对相同的刺激也会有不同的反应,但是这种可变性的确切来源仍然不清楚。为了研究这个问题,我们建立了一个微流体实验系统,该系统可以跟踪多种刺激下单个细胞的反应。我们使用该系统来确定RAW264.7巨噬细胞中G蛋白激活的钙释放的幅度变化通常是外在的,即它们是由于细胞之间长期存在的变化而不是由信号成分的随机激活引起的。在与P2Y家族嘌呤受体相关的反应中,我们估计所观察到的钙释放变异的大约三分之一是受体特异性的。我们进一步证明,P2Y6受体激活下游的信号传导装置是中等饱和的。这些观察将对构建和约束G蛋白偶联钙动力学的单细胞模型有用。

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