Perié Leïla, Duffy Ken R
Institut Curie, PSL Research University, CNRS UMR168, Paris, France.
Sorbonne Universités, UPMC Univ Paris 06, France.
FEBS Lett. 2016 Nov;590(22):4068-4083. doi: 10.1002/1873-3468.12299. Epub 2016 Jul 26.
The dynamic process by which self-renewing stem cells and their offspring proliferate and differentiate to create the erythroid, myeloid and lymphoid lineages of the blood system has long since been an important topic of study. A range of recent single cell and family tracing methodologies such as massively parallel single-cell RNA-sequencing, mass cytometry, integration site barcoding, cellular barcoding and transposon barcoding are enabling unprecedented analysis, dissection and re-evaluation of the haematopoietic tree. In addition to the substantial experimental advances, these new techniques have required significant theoretical development in order to make biological deductions from their data. Here, we review these approaches from both an experimental and inferential point of view, considering their discoveries to date, their capabilities, limitations and opportunities for further development.
自我更新干细胞及其子代细胞增殖并分化以形成血液系统的红系、髓系和淋巴系谱系的动态过程,长期以来一直是重要的研究课题。一系列近期的单细胞和谱系追踪方法,如大规模平行单细胞RNA测序、质谱流式细胞术、整合位点条形码技术、细胞条形码技术和转座子条形码技术,正在使人们能够以前所未有的方式分析、剖析和重新评估造血树。除了取得重大的实验进展外,这些新技术还需要显著的理论发展,以便从其数据中得出生物学推论。在这里,我们从实验和推理的角度对这些方法进行综述,考虑它们迄今为止的发现、能力、局限性以及进一步发展的机会。