Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan; and.
Center for Cellular and Molecular Medicine, Kyushu University Hospital, Fukuoka, Japan.
Blood. 2017 Jun 22;129(25):3332-3343. doi: 10.1182/blood-2016-09-741611. Epub 2017 Mar 23.
The developmental pathway for human megakaryocytes remains unclear, and the definition of pure unipotent megakaryocyte progenitor is still controversial. Using single-cell transcriptome analysis, we have identified a cluster of cells within immature hematopoietic stem- and progenitor-cell populations that specifically expresses genes related to the megakaryocyte lineage. We used CD41 as a positive marker to identify these cells within the CD34CD38IL-3RαCD45RA common myeloid progenitor (CMP) population. These cells lacked erythroid and granulocyte-macrophage potential but exhibited robust differentiation into the megakaryocyte lineage at a high frequency, both in vivo and in vitro. The efficiency and expansion potential of these cells exceeded those of conventional bipotent megakaryocyte/erythrocyte progenitors. Accordingly, the CD41 CMP was defined as a unipotent megakaryocyte progenitor (MegP) that is likely to represent the major pathway for human megakaryopoiesis, independent of canonical megakaryocyte-erythroid lineage bifurcation. In the bone marrow of patients with essential thrombocythemia, the MegP population was significantly expanded in the context of a high burden of Janus kinase 2 mutations. Thus, the prospectively isolatable and functionally homogeneous human MegP will be useful for the elucidation of the mechanisms underlying normal and malignant human hematopoiesis.
人类巨核细胞的发育途径仍不清楚,并且纯单能巨核细胞祖细胞的定义仍存在争议。使用单细胞转录组分析,我们已经在未成熟的造血干/祖细胞群体中鉴定出了一群特定表达与巨核细胞谱系相关基因的细胞。我们使用 CD41 作为阳性标志物,在 CD34CD38IL-3RαCD45RA 共同髓系祖细胞(CMP)群体中鉴定这些细胞。这些细胞缺乏红系和粒细胞-巨噬细胞潜能,但在体内和体外均以高频率表现出向巨核细胞谱系的强大分化能力。这些细胞的效率和扩增潜力超过了传统的双潜能巨核细胞/红细胞祖细胞。因此,CD41 CMP 被定义为单能巨核细胞祖细胞(MegP),它可能代表了人类巨核细胞生成的主要途径,独立于经典的巨核细胞-红细胞谱系分叉。在原发性血小板增多症患者的骨髓中,在 Janus 激酶 2 突变负担较高的情况下,MegP 群体显著扩增。因此,可预期分离和功能均一的人类 MegP 将有助于阐明正常和恶性人类造血的机制。