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使用双筒扫描离子电导显微镜评估 mRNA 定位。

Evaluation of mRNA Localization Using Double Barrel Scanning Ion Conductance Microscopy.

机构信息

Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST) , Saitama 332-0012, Japan.

出版信息

ACS Nano. 2016 Jul 26;10(7):6915-22. doi: 10.1021/acsnano.6b02753. Epub 2016 Jul 14.

Abstract

Information regarding spatial mRNA localization in single cells is necessary for a better understanding of cellular functions in tissues. Here, we report a method for evaluating localization of mRNA in single cells using double-barrel scanning ion conductance microscopy (SICM). Two barrels in a nanopipette were filled with aqueous and organic electrolyte solutions and used for SICM and as an electrochemical syringe, respectively. We confirmed that the organic phase barrel could be used to collect cytosol from living cells, which is a minute but sufficient amount to assess cellular status using qPCR analysis. The water phase barrel could be used for SICM to image topography with subcellular resolution, which could be used to determine positions for analyzing mRNA expression. This system was able to evaluate mRNA localization in single cells. After puncturing the cellular membrane in a minimally invasive manner, using SICM imaging as a guide, we collected a small amount cytosol from different positions within a single cell and showed that mRNA expression depends on cellular position. In this study, we show that SICM imaging can be utilized for the analysis of mRNA localization in single cells. In addition, we fully automated the pipet movement in the XYZ-directions during the puncturing processes, making it applicable as a high-throughput system for collecting cytosol and analyzing mRNA localization.

摘要

关于单个细胞中空间 mRNA 定位的信息对于更好地理解组织中的细胞功能是必要的。在这里,我们报告了一种使用双桶扫描离子电导显微镜 (SICM) 评估单个细胞中 mRNA 定位的方法。纳米管中的两个桶分别填充了水性和有机电解质溶液,分别用于 SICM 和电化学注射器。我们证实有机相桶可用于从活细胞中收集细胞质,这是一个微小但足以使用 qPCR 分析评估细胞状态的量。水相桶可用于 SICM 以亚细胞分辨率成像,这可用于确定分析 mRNA 表达的位置。该系统能够评估单个细胞中的 mRNA 定位。在用 SICM 成像作为指导的微创方式刺穿细胞膜后,我们从单个细胞内的不同位置采集了少量细胞质,并表明 mRNA 表达取决于细胞位置。在这项研究中,我们表明 SICM 成像可用于分析单个细胞中的 mRNA 定位。此外,我们在刺穿过程中完全自动化了 XYZ 方向的移液管运动,使其可作为一种高通量系统,用于收集细胞质和分析 mRNA 定位。

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