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无标记单细胞中动态和瞬时钙信号的成像

Label-Free Imaging of Dynamic and Transient Calcium Signaling in Single Cells.

机构信息

Department of Chemistry, Beijing Key Laboratory for Microanalytical Methods and Instrumentation, Tsinghua University, Beijing 100084 (China).

出版信息

Angew Chem Int Ed Engl. 2015 Nov 9;54(46):13576-80. doi: 10.1002/anie.201505991. Epub 2015 Sep 4.

Abstract

Cell signaling consists of diverse events that occur at various temporal and spatial scales, ranging from milliseconds to hours and from single biomolecules to cell populations. The pathway complexities require the development of new techniques that detect the overall signaling activities and are not limited to quantifying a single event. A plasmonic-based electrochemical impedance microscope (P-EIM) that can provide such data with excellent temporal and spatial resolution and does not require the addition of any labels for detection has now been developed. The highly dynamic and transient calcium signaling activities at the early stage of G-protein-coupled receptor (GPCR) stimulation were thus studied. It could be shown that a subpopulation of cells is more responsive towards agonist stimulation, and the heterogeneity of the local distributions and the transient activities of the ion channels during agonist-activated calcium flux in single HeLa cells were investigated.

摘要

细胞信号转导包括多种事件,这些事件发生在不同的时间和空间尺度上,从毫秒到小时不等,从单个生物分子到细胞群体不等。这些通路的复杂性需要开发新的技术来检测整体信号转导活动,而不仅仅限于量化单个事件。目前已经开发出一种基于等离子体的电化学阻抗显微镜(P-EIM),它可以提供具有出色的时空分辨率的数据,并且不需要添加任何标签进行检测。利用这种技术研究了 G 蛋白偶联受体(GPCR)刺激早期高度动态和瞬时的钙信号转导活动。结果表明,细胞的亚群对激动剂刺激更敏感,并且在单个 HeLa 细胞中激动剂激活钙流期间,离子通道的局部分布和瞬时活性的异质性也被研究。

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