Center for High-Throughput Biology, Department of Physics and Astronomy, and Michael Smith Laboratories, University of British Columbia, Vancouver, BC, Canada V6T 1Z4.
Proc Natl Acad Sci U S A. 2010 Aug 31;107(35):15443-8. doi: 10.1073/pnas.1009320107. Epub 2010 Aug 11.
The hematopoietic system produces a large number of highly specialized cell types that are derived through a hierarchical differentiation process from a common stem cell population. miRNAs are critical players in orchestrating this differentiation. Here, we report the development and application of a high-throughput microfluidic real-time quantitative PCR (RT-qPCR) approach for generating global miRNA profiles for 27 phenotypically distinct cell populations isolated from normal adult mouse hematopoietic tissues. A total of 80,000 RT-qPCR assays were used to map the landscape of miRNA expression across the hematopoietic hierarchy, including rare progenitor and stem cell populations. We show that miRNA profiles allow for the direct inference of cell lineage relations and functional similarity. Our analysis reveals a close relatedness of the miRNA expression patterns in multipotent progenitors and stem cells, followed by a major reprogramming upon restriction of differentiation potential to a single lineage. The analysis of miRNA expression in single hematopoietic cells further demonstrates that miRNA expression is very tightly regulated within highly purified populations, underscoring the potential of single-cell miRNA profiling for assessing compartment heterogeneity.
造血系统产生大量高度特化的细胞类型,这些细胞类型通过一个层次分化过程从一个共同的干细胞群体中衍生而来。miRNA 是协调这种分化的关键因素。在这里,我们报告了一种高通量微流控实时定量 PCR(RT-qPCR)方法的开发和应用,该方法可用于生成 27 种从正常成年小鼠造血组织中分离的表型不同的细胞群体的全局 miRNA 图谱。总共进行了 80,000 次 RT-qPCR 检测,以绘制整个造血系统中 miRNA 表达的图谱,包括罕见的祖细胞和干细胞群体。我们表明,miRNA 图谱可用于直接推断细胞谱系关系和功能相似性。我们的分析表明,多能祖细胞和干细胞中的 miRNA 表达模式密切相关,随后在分化潜能受到限制为单一谱系时发生重大重编程。对单个造血细胞中 miRNA 表达的分析进一步表明,在高度纯化的群体中,miRNA 表达受到非常严格的调控,突出了单细胞 miRNA 分析在评估隔室异质性方面的潜力。