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从福尔马林固定石蜡包埋组织中进行可重复且敏感的微组织 RNA 测序,用于空间基因表达分析。

Reproducible and sensitive micro-tissue RNA sequencing from formalin-fixed paraffin-embedded tissues for spatial gene expression analysis.

机构信息

Research Organization for Nano and Life Innovation, Waseda University, Tokyo, Japan.

Department of Life Science and Medical Bioscience, Waseda University, Tokyo, Japan.

出版信息

Sci Rep. 2022 Nov 14;12(1):19511. doi: 10.1038/s41598-022-23651-6.

Abstract

Spatial transcriptome analysis of formalin-fixed paraffin-embedded (FFPE) tissues using RNA-sequencing (RNA-seq) provides interactive information on morphology and gene expression, which is useful for clinical applications. However, despite the advantages of long-term storage at room temperature, FFPE tissues may be severely damaged by methylene crosslinking and provide less gene information than fresh-frozen tissues. In this study, we proposed a sensitive FFPE micro-tissue RNA-seq method that combines the punching of tissue sections (diameter: 100 μm) and the direct construction of RNA-seq libraries. We evaluated a method using mouse liver tissues at two years after fixation and embedding and detected approximately 7000 genes in micro-punched tissue-spots (thickness: 10 μm), similar to that detected with purified total RNA (2.5 ng) equivalent to the several dozen cells in the spot. We applied this method to clinical FFPE specimens of lung cancer that had been fixed and embedded 6 years prior, and found that it was possible to determine characteristic gene expression in the microenvironment containing tumor and non-tumor cells of different morphologies. This result indicates that spatial gene expression analysis of the tumor microenvironment is feasible using FFPE tissue sections stored for extensive periods in medical facilities.

摘要

使用 RNA 测序 (RNA-seq) 对福尔马林固定石蜡包埋 (FFPE) 组织进行空间转录组分析提供了形态和基因表达的交互信息,这对临床应用很有用。然而,尽管 FFPE 组织在室温下长期储存具有优势,但它们可能会受到亚甲基交联的严重损害,并且提供的基因信息比新鲜冷冻组织少。在这项研究中,我们提出了一种敏感的 FFPE 微组织 RNA-seq 方法,该方法结合了组织切片的打孔(直径:100 μm)和 RNA-seq 文库的直接构建。我们评估了一种使用固定和包埋两年后的小鼠肝组织的方法,并在微打孔组织点(厚度:10 μm)中检测到了大约 7000 个基因,与从几个细胞点中纯化的总 RNA(2.5 ng)相当。我们将该方法应用于已固定和包埋 6 年的肺癌临床 FFPE 标本,发现可以确定包含不同形态肿瘤和非肿瘤细胞的微环境中的特征基因表达。该结果表明,使用在医疗机构中储存时间较长的 FFPE 组织切片进行肿瘤微环境的空间基因表达分析是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ff/9663554/ec566f25d1fa/41598_2022_23651_Fig1_HTML.jpg

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