Wang Nayi, Lu Yao, Chen Zhuo, Fan Rong
Department of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.
Yale Cancer Center, Yale University School of Medicine, New Haven, CT 06520, USA.
Micromachines (Basel). 2019 Mar 27;10(4):215. doi: 10.3390/mi10040215.
MicroRNAs are a class of small RNA molecules that regulate the expression of mRNAs in a wide range of biological processes and are implicated in human health and disease such as cancers. How to measure microRNA profiles in single cells with high throughput is essential to the development of cell-based assays for interrogating microRNA-mediated intratumor heterogeneity and the design of new lab tests for diagnosis and monitoring of cancers. Here, we report on an in situ hybridization barcoding workflow implemented in a sub-nanoliter microtrough array chip for high-throughput and multiplexed microRNA detection at the single cell level. The microtroughs are used to encapsulate single cells that are fixed, permeabilized, and pre-incubated with microRNA detection probes, each of which consists of a capture strand complementary to specific microRNA and a unique reporter strand that can be photocleaved in the microtroughs and subsequently detected by an array of DNA barcodes patterned on the bottom of the microtroughs. In this way, the measurement of reporter strands released from single cells is a surrogate for detecting single-cell microRNA profiles. This approach permits direct measurement of microRNAs without PCR amplification owing to the small volume (<1 nL) of microtroughs. It offers high throughput and high multiplexing capability for evaluating microRNA heterogeneity in single cells, representing a new approach toward microRNA-based diagnosis and monitoring of complex human diseases.
微小RNA是一类小RNA分子,在广泛的生物过程中调节mRNA的表达,并与人类健康和疾病(如癌症)有关。如何高通量地测量单细胞中的微小RNA谱对于开发用于研究微小RNA介导的肿瘤内异质性的细胞检测方法以及设计用于癌症诊断和监测的新实验室检测至关重要。在此,我们报告了一种在亚纳升微槽阵列芯片中实现的原位杂交条形码工作流程,用于在单细胞水平上进行高通量和多重微小RNA检测。微槽用于封装单细胞,这些单细胞经过固定、通透处理,并与微小RNA检测探针进行预孵育,每个探针由与特定微小RNA互补的捕获链和独特的报告链组成,该报告链可在微槽中光裂解,随后由微槽底部图案化的一系列DNA条形码进行检测。通过这种方式,从单细胞释放的报告链的测量是检测单细胞微小RNA谱的替代方法。由于微槽体积小(<1 nL),这种方法无需PCR扩增即可直接测量微小RNA。它为评估单细胞中的微小RNA异质性提供了高通量和高多重能力,代表了一种基于微小RNA的复杂人类疾病诊断和监测的新方法。