Ziegler B, Testa U, Condorelli G, Vitelli L, Valtieri M, Peschle C
Department of Medicine, Eberhard-Karls University Tübingen, Germany.
Stem Cells. 1998;16 Suppl 1:51-73. doi: 10.1002/stem.5530160808.
The rarity of hematopoietic stem and progenitor cells (HSCs, HPCs) has hampered the analysis of cellular and molecular mechanisms underlying early hematopoiesis. Methodology for HPC purification has partially offset this limitation. A further hurdle has been represented by the heterogeneity of the analyzed HPC/precursor populations: recently, development of unilineage HPC differentiation cultures has provided homogeneous populations of hematopoietic cells, particularly in the early differentiation state, i.e., populations pertaining to a single lineage and a restricted stage of differentiation/maturation, but sufficiently large for cellular/molecular analysis. This report focuses on the development and characterization of the unilineage HPC differentiation culture systems. A section is devoted to selected cellular and molecular mechanisms underlying hematopoiesis, which have been investigated by the HPC unilineage culture approach. Finally, recent advances in the development of HPC unilineage cultures at single cell level are discussed.
造血干细胞和祖细胞(HSCs、HPCs)的稀缺阻碍了对早期造血过程中细胞和分子机制的分析。HPC纯化方法部分弥补了这一局限性。另一个障碍是所分析的HPC/前体细胞群体的异质性:最近,单系HPC分化培养技术的发展提供了均一的造血细胞群体,特别是在早期分化状态,即属于单一谱系和有限分化/成熟阶段的群体,但数量足够大,可用于细胞/分子分析。本报告重点介绍单系HPC分化培养系统的开发和特性。其中一部分专门讨论了通过HPC单系培养方法研究的造血过程中特定的细胞和分子机制。最后,讨论了单细胞水平HPC单系培养技术的最新进展。