Snoeck Hans-Willem
Columbia Center for Stem Cell Therapies/Columbia Center for Human Development, Department of Medicine.
Department of Microbiology and Immunology, Columbia University Vagelos College of Physicians and Surgeons.
Curr Opin Hematol. 2025 Jul 1;32(4):213-220. doi: 10.1097/MOH.0000000000000871. Epub 2025 Apr 21.
Megakaryocytes are large, polyploid cells that produce platelets and originate from hematopoietic stem cells (HSCs) in the bone marrow. While in the classical paradigm, megakaryocytes are generated in a stepwise fashion through increasingly committed progenitor stages, studies using in-vivo barcoding, transplantation, and in-vitro culture have suggested that, in addition, a more direct pathway existed. The relevance of this direct pathway and its functional and phenotypic characteristics were unclear, however.
Recent publications using fate-mapping and single-cell transplantation now unequivocally demonstrate the existence of a direct megakaryocyte differentiation pathway, provide molecular characterization, and indicate distinct roles and regulation of both pathways. The direct pathway originates from a separate subset of 'top' HSCs, is enhanced by hematopoietic stress, inflammation and aging, bypasses multipotential progenitors, may be more active in myeloproliferative neoplasms, and generates phenotypically distinct megakaryocyte progenitors and more reactive platelets.
Novel insights into the direct megakaryocyte differentiation pathway provide a deeper understanding of HSC biology, hematological recovery after myeloablation, and aging of the hematopoietic system, and suggest that this pathway may contribute to the increase in thrombotic incidents with age and in myeloproliferative neoplasms.
巨核细胞是大型多倍体细胞,可产生血小板,起源于骨髓中的造血干细胞(HSC)。在经典模式中,巨核细胞通过逐渐分化的祖细胞阶段逐步生成,但使用体内条形码技术、移植和体外培养的研究表明,此外还存在一条更直接的途径。然而,这条直接途径的相关性及其功能和表型特征尚不清楚。
最近使用命运图谱和单细胞移植的出版物现在明确证明了直接巨核细胞分化途径的存在,提供了分子特征,并指出了两条途径的不同作用和调控。直接途径起源于“顶端”HSC的一个单独亚群,在造血应激、炎症和衰老时增强,绕过多能祖细胞,在骨髓增殖性肿瘤中可能更活跃,并产生表型不同的巨核细胞祖细胞和反应性更强的血小板。
对直接巨核细胞分化途径的新见解为深入理解HSC生物学、骨髓消融后的血液学恢复以及造血系统衰老提供了帮助,并表明该途径可能导致年龄增长和骨髓增殖性肿瘤中血栓事件的增加。