Giebel Bernd, Punzel Michael
Institute for Transplantation Diagnostics and Cellular Therapeutics, Heinrich Heine University, Düsseldorf, Germany.
Biol Chem. 2008 Jul;389(7):813-24. doi: 10.1515/BC.2008.092.
Hematopoietic stem cells have the potential to develop into multipotent and different lineage-restricted progenitor cells that subsequently generate all mature blood cell types. The classical model of hematopoietic lineage commitment proposes a first restriction point at which all multipotent hematopoietic progenitor cells become committed either to the lymphoid or to the myeloid development, respectively. Recently, this model has been challenged by the identification of murine as well as human hematopoietic progenitor cells with lymphoid differentiation capabilities that give rise to a restricted subset of the myeloid lineages. As the classical model does not include cells with such capacities, these findings suggest the existence of alternative developmental pathways that demand the existence of additional branches in the classical hematopoietic tree. Together with some phenotypic criteria that characterize different subsets of multipotent and lineage-restricted progenitor cells, we summarize these recent findings here.
造血干细胞有潜力发育成多能和不同谱系限制的祖细胞,随后产生所有成熟血细胞类型。造血谱系定向的经典模型提出了一个初始限制点,在这个点上,所有多能造血祖细胞分别定向于淋巴样或髓样发育。最近,这一模型受到了挑战,因为已鉴定出具有淋巴样分化能力的小鼠和人类造血祖细胞,这些细胞可产生髓系谱系的一个受限亚群。由于经典模型不包括具有这种能力的细胞,这些发现提示存在替代发育途径,这需要在经典造血树中存在额外的分支。我们结合表征多能和谱系限制祖细胞不同亚群的一些表型标准,在此总结这些最新发现。