发布: 2018年06月20日第8卷第12期 DOI: 10.21769/BioProtoc.2892 浏览次数: 6468
评审: Ivan ZanoniShanie Saghafian-HedengrenAnonymous reviewer(s)
Abstract
The protocol described here has been developed to detect RNA at the single cell level. Fluorescent probes hybridize to target RNAs and are detected by flow cytometry after multiple amplification steps. Different types of RNA can be detected such as mRNA, long noncoding RNA, viral RNA or telomere RNA and up to 4 different target probes can be used simultaneously. We used this protocol to specifically measure the expression of two transcription factor mRNAs, MAFB and IRF4, in human monocytes.
Keywords: RNA (RNA)Background
RT-qPCR is one major technique used to easily assess RNA expression. Cells are lysed and analyzed in bulk. Hence, cell heterogeneity is lost. In particular, it is impossible using RT-qPCR to address whether subpopulations may be identified based on the expression of RNA. RNA Fluorescent In Situ Hybridization (FISH) is a way to detect RNA in single cells. This technique requires hybridization of fluorescent probes on RNA targets that are then detected using an imaging system such as a confocal microscope. However, this method is time-consuming and allows the analysis of a limited number of individual cells.
We demonstrated by RT-qPCR that human monocytes cultured in RPMI with M-CSF, IL-4, and TNFa express after three hours the transcription factors MAFB and IRF4 (Goudot et al., 2017). MAFB and IRF4 are involved in the differentiation of monocytes into monocyte-derived macrophages (mo-mac) and monocyte-derived DC (mo-DC) respectively. To decipher whether monocytes express both transcription factors or if this expression is mutually exclusive, we performed in situ hybridization coupled to flow cytometry using PrimeFlow RNA assay.
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版权信息
© 2018 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Coillard, A. and Segura, E. (2018). Visualization of RNA at the Single Cell Level by Fluorescent in situ Hybridization Coupled to Flow Cytometry. Bio-protocol 8(12): e2892. DOI: 10.21769/BioProtoc.2892.
分类
免疫学 > 免疫细胞染色 > 流式细胞术
发育生物学 > 细胞生长和命运决定 > 分化
细胞生物学 > 细胞染色 > 核酸
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