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激光捕获显微切割:应使用紫外激光还是红外激光?

Laser capture microdissection: should an ultraviolet or infrared laser be used?

机构信息

Laboratory for Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent University, B-9000 Ghent, Belgium.

出版信息

Anal Biochem. 2013 Aug 15;439(2):88-98. doi: 10.1016/j.ab.2013.04.023. Epub 2013 Apr 30.

Abstract

Laser capture microdissection (LCM) is a well-established cell separation technique. It combines microscopy with laser beam technology and allows targeting of specific cells or tissue regions that need to be separated from others. Consequently, this biological material can be used for genome or transcriptome analyses. Appropriate methods of sample preparation, however, are crucial for the success of downstream molecular analysis. The aim of this study was to objectively compare the two main LCM systems, one based on an ultraviolet (UV) laser and the other based on an infrared (IR) laser, on different criteria ranging from user-friendliness to sample quality. The comparison was performed on two types of samples: peripheral blood mononuclear cells and blastocysts. The UV laser LCM system had several advantages over the IR laser LCM system. Not only does the UV system allow faster and more precise sample collection, but also the obtained samples-even single cell samples-can be used for DNA extraction and downstream polymerase chain reaction (PCR) applications. RNA-based applications are more challenging for both LCM systems. Although sufficient RNA can be extracted from as few as 10 cells for reverse transcription quantitative PCR (RT-qPCR) analysis, the low RNA quality should be taken into account when designing the RT-qPCR assays.

摘要

激光捕获显微切割(LCM)是一种成熟的细胞分离技术。它结合了显微镜和激光束技术,可以针对需要与其他细胞或组织区域分离的特定细胞或组织区域进行靶向。因此,这种生物材料可用于基因组或转录组分析。然而,适当的样品制备方法对于下游分子分析的成功至关重要。本研究旨在客观比较两种主要的 LCM 系统,一种基于紫外线(UV)激光,另一种基于红外线(IR)激光,从用户友好性到样品质量等不同标准进行比较。比较在两种类型的样品上进行:外周血单核细胞和囊胚。UV 激光 LCM 系统相对于 IR 激光 LCM 系统具有几个优势。不仅 UV 系统允许更快、更精确的样品采集,而且获得的样品——即使是单细胞样品——也可用于 DNA 提取和下游聚合酶链反应(PCR)应用。基于 RNA 的应用对两种 LCM 系统来说都更具挑战性。尽管对于逆转录定量 PCR(RT-qPCR)分析,从低至 10 个细胞中即可提取足够的 RNA,但在设计 RT-qPCR 检测时应考虑到 RNA 质量较低的问题。

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