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通过单分子成像技术揭示的盘基网柄菌细胞趋化反应中的随机信号输入

Stochastic signal inputs for chemotactic response in Dictyostelium cells revealed by single molecule imaging techniques.

作者信息

Miyanaga Yukihiro, Matsuoka Satomi, Yanagida Toshio, Ueda Masahiro

机构信息

Laboratories for Nanobiology, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

Biosystems. 2007 Apr;88(3):251-60. doi: 10.1016/j.biosystems.2006.07.011. Epub 2006 Nov 10.

Abstract

Chemotactic cells can exhibit extreme sensitivity to chemical gradients. Theoretical estimations of the signal inputs required for chemotaxis suggest that the response can be achieved under the strong influence of stochastic input noise generated by the receptors during the transmembrane signaling. This arises a fundamental question regarding the mechanisms for directional sensing: how do cells obtain reliable information regarding gradient direction by using stochastically operating receptors and the downstream molecules? To address this question, we have developed single molecule imaging techniques to visualize signaling molecules responsible for chemotaxis in living Dictyostelium cells, allowing us to monitor the stochastic signaling processes directly. Single molecule imaging of a chemoattractant bound to a receptor demonstrates that signal inputs fluctuate with time and space. Downstream signaling molecules, such as PTEN and a PH domain-containing protein that are constituent parts of chemotactic signaling system, can also be followed at single molecule level in living cells, illuminating the stochastic nature of chemotactic signaling processes. In this report, we start with a brief introduction of chemotactic response of the eukaryotic cells, followed by an explanation for single molecule imaging techniques, and finally discuss these applications to chemotactic signaling system of Dictyostelium cells.

摘要

趋化细胞能够对化学梯度表现出极高的敏感性。趋化作用所需信号输入的理论估计表明,在跨膜信号传导过程中,受体产生的随机输入噪声的强烈影响下,细胞能够实现这种响应。这就引发了一个关于定向感知机制的基本问题:细胞如何通过使用随机运作的受体和下游分子来获取有关梯度方向的可靠信息?为了解决这个问题,我们开发了单分子成像技术,以可视化负责盘基网柄菌细胞趋化作用的信号分子,从而使我们能够直接监测随机信号传导过程。与受体结合的趋化因子的单分子成像表明,信号输入随时间和空间而波动。下游信号分子,如磷脂酰肌醇-3,4,5-三磷酸酶(PTEN)和趋化信号系统组成部分的含PH结构域的蛋白质,也可以在活细胞中以单分子水平进行追踪,从而揭示趋化信号传导过程的随机性。在本报告中,我们首先简要介绍真核细胞的趋化反应,接着解释单分子成像技术,最后讨论这些技术在盘基网柄菌细胞趋化信号系统中的应用。

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