Understanding hematopoiesis from a single-cell standpoint

被引:3
|
作者
Kokkaliaris, Konstantinos D. [1 ]
Lucas, Daniel [2 ]
Beeman, Isabel [3 ]
Kent, David G. [4 ,5 ]
Perie, Leila [6 ]
机构
[1] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Cell Syst Dynam Res Grp, Basel, Switzerland
[2] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI USA
[3] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA USA
[4] Univ Cambridge, Dept Haematol, Wellcome Trust, Cambridge, England
[5] Univ Cambridge, MRC, Cambridge Stein Cell Inst, Cambridge, England
[6] PSL Res Univ, Inst Curie, Paris, France
基金
英国医学研究理事会;
关键词
STEM-CELLS; HETEROGENEITY; PROGENY;
D O I
10.1016/j.exphem.2016.03.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The cellular diversity of the hematopoietic system has been extensively studied, and a plethora of cell surface markers have been used to discriminate and prospectively purify different blood cell types. However, even within phenotypically identical fractions of hematopoietic stem and progenitor cells or lineage-restricted progenitors, significant functional heterogeneity is observed when single cells are analyzed. To address these challenges, researchers are now using techniques to follow single cells and their progeny to improve our understanding of the underlying functional heterogeneity. On November 19, 2015, Dr. David Kent and Dr. Leila Perie, two emerging young group leaders, presented their recent efforts to dissect the functional properties of individual cells with a webinar series organized by the International Society for Experimental Hematology. Here, we provide a summary of the presented methods for cell labeling and clonal tracking and discuss how these different techniques have been employed to study hematopoiesis. (C) 2016 ISEH - International Society for Experimental Hematology. Published by Elsevier Inc.
引用
收藏
页码:447 / 450
页数:4
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