Kristiansen Trine A, Doyle Alexander, Yuan Joan
Division of Molecular Hematology, Department of Laboratory Medicine, Lund Stem Cell Center, Faculty of Medicine, Lund University, Lund, Sweden.
Bio Protoc. 2017 Apr 20;7(8):e2242. doi: 10.21769/BioProtoc.2242.
Cellular barcoding enables the dissection of clonal dynamics in heterogeneous cell populations through single cell lineage tracing. The labeling of hematopoietic stem and progenitor cells (HSPCs) with unique and heritable DNA barcodes, makes it possible to resolve donor cell heterogeneity in terms of differentiation potential and lineage bias at the single cell level, through subsequent transplantation and high-throughput sequencing. Furthermore, cellular barcoding allows for bona fide hematopoietic stem cells (HSCs) to be defined based on functional rather than immunophenotypic parameters. This protocol describes the work flow of lentiviral cellular barcoding, tracking 14.5 days post coitum (d.p.c.) fetal liver (FL) Lineage-ScacKit (LSK) HSPCs following long-term reconstitution (Figure 1) ( Kristiansen , 2016 ), but can be adapted to the cell type or time frame of choice. Figure 1.Summary of experimental workflow ( Naik , 2013 ).
细胞条形码技术能够通过单细胞谱系追踪来剖析异质细胞群体中的克隆动态。用独特且可遗传的DNA条形码标记造血干细胞和祖细胞(HSPCs),通过后续的移植和高通量测序,能够在单细胞水平上解析供体细胞在分化潜能和谱系偏向方面的异质性。此外,细胞条形码技术使得真正的造血干细胞(HSCs)能够基于功能而非免疫表型参数来定义。本方案描述了慢病毒细胞条形码技术的工作流程,对交配后14.5天(d.p.c.)的胎肝(FL)谱系 - Sca - Kit(LSK)HSPCs进行长期重建后的追踪(图1)(克里斯蒂安森,2016年),但可根据所选的细胞类型或时间框架进行调整。图1.实验工作流程总结(奈克,2013年)