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同时成像内质网和胞质 Ca2+ 动力学揭示植物中长距离内质网 Ca2+ 波。

Simultaneous imaging of ER and cytosolic Ca2+ dynamics reveals long-distance ER Ca2+ waves in plants.

机构信息

Department of Biosciences, University of Milan, Milan 20133, Italy.

Department of Physics, Politecnico di Milano, Milan 20133, Italy.

出版信息

Plant Physiol. 2021 Oct 5;187(2):603-617. doi: 10.1093/plphys/kiab251.

Abstract

Calcium ions (Ca2+) play a key role in cell signaling across organisms. In plants, a plethora of environmental and developmental stimuli induce specific Ca2+ increases in the cytosol as well as in different cellular compartments including the endoplasmic reticulum (ER). The ER represents an intracellular Ca2+ store that actively accumulates Ca2+ taken up from the cytosol. By exploiting state-of-the-art genetically encoded Ca2+ indicators, specifically the ER-GCaMP6-210 and R-GECO1, we report the generation and characterization of an Arabidopsis (Arabidopsis thaliana) line that allows for simultaneous imaging of Ca2+ dynamics in both the ER and cytosol at different spatial scales. By performing analyses in single cells, we precisely quantified (1) the time required by the ER to import Ca2+ from the cytosol into the lumen and (2) the time required to observe a cytosolic Ca2+ increase upon the pharmacological inhibition of the ER-localized P-Type IIA Ca2+-ATPases. Furthermore, live imaging of mature, soil-grown plants revealed the existence of a wounding-induced, long-distance ER Ca2+ wave propagating in injured and systemic rosette leaves. This technology enhances high-resolution analyses of intracellular Ca2+ dynamics at the cellular level and in adult organisms and paves the way to develop new methodologies aimed at defining the contribution of subcellular compartments in Ca2+ homeostasis and signaling.

摘要

钙离子(Ca2+)在生物体内的细胞信号转导中起着关键作用。在植物中,大量的环境和发育刺激会在细胞质以及内质网(ER)等不同细胞区室中诱导特定的 Ca2+增加。ER 代表一个细胞内的 Ca2+储存库,它会主动积累从细胞质中摄取的 Ca2+。通过利用最先进的遗传编码 Ca2+指示剂,特别是 ER-GCaMP6-210 和 R-GECO1,我们报告了一种拟南芥(Arabidopsis thaliana)系的产生和特征,该系允许在不同的空间尺度上同时对 ER 和细胞质中的 Ca2+动力学进行成像。通过在单细胞中进行分析,我们精确地量化了:(1)ER 将 Ca2+从细胞质中导入腔室所需的时间;(2)观察到细胞溶质 Ca2+增加所需的时间,在药理学抑制 ER 定位的 P 型 IIA Ca2+-ATPases 时。此外,对成熟、土壤生长的植物进行的活体成像显示,存在一种由创伤诱导的、长距离的 ER Ca2+波,在受伤和系统的莲座叶中传播。这项技术增强了细胞水平和成年生物体中细胞内 Ca2+动力学的高分辨率分析,并为开发新的方法学铺平了道路,旨在确定亚细胞区室在 Ca2+稳态和信号转导中的贡献。

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