Department of Paediatrics and.
Medical Research Council (MRC) Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Blood. 2019 Sep 26;134(13):1059-1071. doi: 10.1182/blood.2019001289. Epub 2019 Aug 5.
Human lymphopoiesis is a dynamic lifelong process that starts in utero 6 weeks postconception. Although fetal B-lymphopoiesis remains poorly defined, it is key to understanding leukemia initiation in early life. Here, we provide a comprehensive analysis of the human fetal B-cell developmental hierarchy. We report the presence in fetal tissues of 2 distinct CD19 B-progenitors, an adult-type CD10+ve ProB-progenitor and a new CD10-ve PreProB-progenitor, and describe their molecular and functional characteristics. PreProB-progenitors and ProB-progenitors appear early in the first trimester in embryonic liver, followed by a sustained second wave of B-progenitor development in fetal bone marrow (BM), where together they form >40% of the total hematopoietic stem cell/progenitor pool. Almost one-third of fetal B-progenitors are CD10-ve PreProB-progenitors, whereas, by contrast, PreProB-progenitors are almost undetectable (0.53% ± 0.24%) in adult BM. Single-cell transcriptomics and functional assays place fetal PreProB-progenitors upstream of ProB-progenitors, identifying them as the first B-lymphoid-restricted progenitor in human fetal life. Although fetal BM PreProB-progenitors and ProB-progenitors both give rise solely to B-lineage cells, they are transcriptionally distinct. As with their fetal counterparts, adult BM PreProB-progenitors give rise only to B-lineage cells in vitro and express the expected B-lineage gene expression program. However, fetal PreProB-progenitors display a distinct, ontogeny-related gene expression pattern that is not seen in adult PreProB-progenitors, and they share transcriptomic signatures with CD10-ve B-progenitor infant acute lymphoblastic leukemia blast cells. These data identify PreProB-progenitors as the earliest B-lymphoid-restricted progenitor in human fetal life and suggest that this fetal-restricted committed B-progenitor might provide a permissive cellular context for prenatal B-progenitor leukemia initiation.
人类淋巴造血是一个始于受孕后 6 周的动态终生过程。虽然胎儿 B 细胞造血仍未得到充分定义,但它是理解生命早期白血病起始的关键。在这里,我们提供了人类胎儿 B 细胞发育层次结构的全面分析。我们报告了在胎儿组织中存在 2 种不同的 CD19 B 祖细胞,一种是成人型 CD10+ve ProB 祖细胞,另一种是新的 CD10-ve PreProB 祖细胞,并描述了它们的分子和功能特征。PreProB 祖细胞和 ProB 祖细胞在胚胎肝脏的第一个三个月早期出现,随后在胎儿骨髓(BM)中出现持续的第二波 B 祖细胞发育,在那里它们共同构成了>40%的总造血干细胞/祖细胞池。几乎三分之一的胎儿 B 祖细胞是 CD10-ve PreProB 祖细胞,相比之下,PreProB 祖细胞在成人 BM 中几乎无法检测到(0.53%±0.24%)。单细胞转录组学和功能测定将胎儿 PreProB 祖细胞置于 ProB 祖细胞的上游,将其鉴定为人类胎儿生命中第一个 B 淋巴细胞受限的祖细胞。虽然胎儿 BM PreProB 祖细胞和 ProB 祖细胞都仅产生 B 细胞谱系细胞,但它们在转录上是不同的。与它们的胎儿对应物一样,成人 BM PreProB 祖细胞仅在体外产生 B 细胞谱系细胞,并表达预期的 B 细胞谱系基因表达程序。然而,胎儿 PreProB 祖细胞显示出独特的、与个体发生相关的基因表达模式,在成人 PreProB 祖细胞中没有看到,并且它们与 CD10-ve B 祖细胞婴儿急性淋巴细胞白血病母细胞具有相似的转录组特征。这些数据将 PreProB 祖细胞鉴定为人类胎儿生命中最早的 B 淋巴细胞受限祖细胞,并表明这种胎儿受限的定向 B 祖细胞可能为产前 B 祖细胞白血病的起始提供了一个允许的细胞环境。