Luc Sidinh, Buza-Vidas Natalija, Jacobsen Sten Eirik W
Haematopoietic Stem Cell Laboratory, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
Semin Immunol. 2008 Aug;20(4):213-20. doi: 10.1016/j.smim.2008.07.005. Epub 2008 Aug 27.
The prevailing model for adult hematopoiesis postulates that the first lineage commitment step results in a strict separation of common myeloid and common lymphoid pathways. However, the recent identification of granulocyte/monocyte (GM)-lymphoid restricted lymphoid-primed multipotent progenitors (LMPPs) and primitive common myeloid progenitors (CMPs) within the "HSC" compartment provide compelling support for establishment of independent GM-megakaryocyte/erythroid (GM-MkE) and GM-lymphoid commitment pathways as decisive early lineage fate decisions. These changes in lineage potentials are corroborated by corresponding changes in multilineage transcriptional priming, as LMPPs down-regulate MkE priming but become GM-lymphoid transcriptionally primed, whereas CMPs are GM-MkE primed. These distinct biological and molecular relationships are established already in the fetal liver.
成人造血的主流模型假定,第一个谱系定向步骤会导致共同髓系和共同淋巴系途径的严格分离。然而,最近在“造血干细胞(HSC)”区室中鉴定出粒细胞/单核细胞(GM)-淋巴系受限的淋巴系启动多能祖细胞(LMPP)和原始共同髓系祖细胞(CMP),这为独立的GM-巨核细胞/红细胞(GM-MkE)和GM-淋巴系定向途径的建立提供了有力支持,这是早期决定性的谱系命运决定。谱系潜能的这些变化通过多谱系转录启动的相应变化得到证实,因为LMPP下调MkE启动但在转录上成为GM-淋巴系启动,而CMP则是GM-MkE启动。这些独特的生物学和分子关系在胎儿肝脏中就已确立。