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分化途径决定成人巨核细胞生成的功能输出。

Differentiation route determines the functional outputs of adult megakaryopoiesis.

机构信息

State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.

Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Immunity. 2024 Mar 12;57(3):478-494.e6. doi: 10.1016/j.immuni.2024.02.006. Epub 2024 Mar 5.

Abstract

Emerging evidence has revealed a direct differentiation route from hematopoietic stem cells to megakaryocytes (direct route), in addition to the classical differentiation route through a series of restricted hematopoietic progenitors (stepwise route). This raises the question of the importance of two alternative routes for megakaryopoiesis. Here, we developed fate-mapping systems to distinguish the two routes, comparing their quantitative and functional outputs. We found that megakaryocytes were produced through the two routes with comparable kinetics and quantity under homeostasis. Single-cell RNA sequencing of the fate-mapped megakaryocytes revealed that the direct and stepwise routes contributed to the niche-supporting and immune megakaryocytes, respectively, but contributed to the platelet-producing megakaryocytes together. Megakaryocytes derived from the two routes displayed different activities and were differentially regulated by chemotherapy and inflammation. Our work links differentiation route to the heterogeneity of megakaryocytes. Alternative differentiation routes result in variable combinations of functionally distinct megakaryocyte subpopulations poised for different physiological demands.

摘要

新出现的证据表明,造血干细胞向巨核细胞的分化除了经典的通过一系列受限的造血祖细胞的逐步分化途径(逐步途径)之外,还有直接分化途径。这就提出了巨核细胞生成的两种替代途径的重要性问题。在这里,我们开发了命运映射系统来区分这两种途径,比较它们的定量和功能输出。我们发现,在体内平衡下,巨核细胞通过两种途径以相似的动力学和数量产生。对命运映射的巨核细胞进行单细胞 RNA 测序表明,直接途径和逐步途径分别有助于支持生态位和免疫巨核细胞,但共同有助于产生血小板的巨核细胞。来自两种途径的巨核细胞显示出不同的活性,并且受到化疗和炎症的不同调节。我们的工作将分化途径与巨核细胞的异质性联系起来。替代的分化途径导致功能不同的巨核细胞亚群的可变组合,这些亚群为不同的生理需求做好了准备。

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