Suppr超能文献

慢病毒条形码标记与胎儿肝脏造血干细胞和祖细胞移植

Lentiviral Barcode Labeling and Transplantation of Fetal Liver Hematopoietic Stem and Progenitor Cells.

作者信息

Kristiansen Trine A, Doyle Alexander, Yuan Joan

机构信息

Division of Molecular Hematology, Department of Laboratory Medicine, Lund Stem Cell Center, Faculty of Medicine, Lund University, Lund, Sweden.

出版信息

Bio Protoc. 2017 Apr 20;7(8):e2242. doi: 10.21769/BioProtoc.2242.

Abstract

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 ).

摘要

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)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2951/8410422/14360adbbebf/BioProtoc-7-08-2242-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验