Kraus Petra, Yerden Rachel, Sipes Darren, Sur Shantanu, Lufkin Thomas
Department of Biology, Clarkson University, 8 Clarkson Avenue, Potsdam, NY, 13699-5805, USA.
Cytotechnology. 2018 Feb;70(1):185-192. doi: 10.1007/s10616-017-0132-1. Epub 2017 Aug 10.
Cells are often characterized by their gene expression profile. However, commonly used methods to detect mRNA require cell pooling and could therefore mask differences in gene expression within heterogeneous cell populations. qPISH allows for the analysis of both qualitative and quantitative (q) gene expression on cultured cells for quality control measures with single cell resolution. qPISH was optimized for the subsequent use of two alkaline phosphatase substrates in combination with a cell nucleus count to allow for accurate quantification of gene expression per cell and simultaneously qualitative assessment of potential culture population drift or heterogeneity. As proof of principle the assay was applied to cell lines derived from different areas of the bovine intervertebral disc, showing significant difference in the expression of Col1a1, Col2a1, Acan and Sox9. Furthermore, the assay served to explore a potential impact on cultured cells when substituting a critical media component, fetal bovine serum (FBS), suggesting no significant difference in gene expression for the biomarkers analyzed. As a tool, qPISH serves as an accurate quality control with single cell resolution for cultured cells.
细胞通常由其基因表达谱来表征。然而,常用的检测mRNA的方法需要细胞汇集,因此可能掩盖异质细胞群体内基因表达的差异。定量原位杂交(qPISH)能够在单细胞分辨率下,对培养细胞进行定性和定量(q)基因表达分析,用于质量控制。qPISH经过优化,可随后结合使用两种碱性磷酸酶底物和细胞核计数,以便准确量化每个细胞的基因表达,并同时定性评估潜在的培养群体漂移或异质性。作为原理验证,该检测方法应用于源自牛椎间盘不同区域的细胞系,结果显示Col1a1、Col2a1、Acan和Sox9的表达存在显著差异。此外,该检测方法还用于探究替代关键培养基成分胎牛血清(FBS)时对培养细胞的潜在影响,结果表明所分析的生物标志物的基因表达没有显著差异。作为一种工具,qPISH可在单细胞分辨率下对培养细胞进行准确的质量控制。