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利用 GFP 生物传感器进行 Ca2+ 、氧化还原状态、ROS 和 pH 的高分辨率成像。

High-resolution imaging of Ca2+ , redox status, ROS and pH using GFP biosensors.

机构信息

Department of Botany, University of Wisconsin, Birge Hall, 430 Lincoln Drive, Madison, WI 53706, USA.

出版信息

Plant J. 2012 Apr;70(1):118-28. doi: 10.1111/j.1365-313X.2012.04917.x.

DOI:10.1111/j.1365-313X.2012.04917.x
PMID:22449047
Abstract

Many plant response systems are linked to complex dynamics in signaling molecules such as Ca(2+) and reactive oxygen species (ROS) and to pH. Regulatory changes in these molecules can occur in the timeframe of seconds and are often limited to specific subcellular locales. Thus, to understand how Ca(2+) , ROS and pH form part of plants' regulatory networks, it is essential to capture their rapid dynamics with resolutions that span the whole plant to subcellular dimensions. Defining the spatio-temporal signaling 'signatures' of these regulators at high resolution has now been greatly facilitated by the generation of plants expressing a range of GFP-based bioprobes. For Ca(2+) and pH, probes such as the yellow cameleon Ca(2+) sensors (principally YC2.1 and 3.6) or the pHluorin and H148D pH sensors provide a robust suite of tools to image changes in these ions. For ROS, the tools are much more limited, with the GFP-based H(2) O(2) sensor Hyper representing a significant advance for the field. However, with this probe, its marked pH sensitivity provides a key challenge to interpretation without using appropriate controls to test for potentially coupled pH-dependent changes. Most of these Ca(2+) -, ROS- and pH-imaging biosensors are compatible with the standard configurations of confocal microscopes available to many researchers. These probes therefore represent a readily accessible toolkit to monitor cellular signaling. Their use does require appreciation of a minimal set of controls but these are largely related to ensuring that neither the probe itself nor the imaging conditions used perturb the biology of the plant under study.

摘要

许多植物反应系统与信号分子(如 Ca(2+) 和活性氧(ROS)和 pH)的复杂动力学有关。这些分子的调节变化可以在几秒钟的时间内发生,并且通常仅限于特定的亚细胞位置。因此,要了解 Ca(2+)、ROS 和 pH 如何构成植物调节网络的一部分,就必须以跨越整个植物到亚细胞维度的分辨率来捕捉它们的快速动态。通过生成表达一系列 GFP 基生物探针的植物,现在极大地方便了定义这些调节剂的快速动态“信号特征”的时空分辨率。对于 Ca(2+)和 pH,探针如黄色 Cameleon Ca(2+)传感器(主要是 YC2.1 和 3.6)或 pHluorin 和 H148D pH 传感器为这些离子的变化提供了一套强大的成像工具。对于 ROS,工具要有限得多,基于 GFP 的 H(2)O(2)传感器 Hyper 是该领域的重大进展。然而,对于这种探针,其明显的 pH 敏感性在没有使用适当的对照来测试潜在的耦合 pH 依赖性变化的情况下,对解释提出了关键挑战。这些 Ca(2+)、ROS 和 pH 成像生物传感器中的大多数都与许多研究人员可用的标准共聚焦显微镜配置兼容。因此,这些探针代表了一种易于访问的工具包,可以监测细胞信号。它们的使用确实需要了解一组最小的控制,但这些主要与确保探针本身或使用的成像条件不会干扰正在研究的植物的生物学有关。

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