1021 – DIFFERENTIATION ROUTE DETERMINES THE FUNCTIONAL OUTPUTS OF ADULT MEGAKARYOPOIESIS

IF 2.5 4区 医学 Q2 HEMATOLOGY Experimental hematology Pub Date : 2024-08-01 DOI:10.1016/j.exphem.2024.104322
Bo Zhou , Jingjing Li
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Abstract

One of the breakthroughs in hematopoietic stem cell (HSC) field over the last decade is the discovery of two alternative differentiation routes from primitive HSCs to mature megakaryocytes: one through the stepwise hematopoietic hierarchy (stepwise route), and the other by direct differentiation (direct route). This raises a fundamental question of the physiological importance of two alternative differentiation routes for megakaryopoiesis. A major challenge in addressing this question is the lack of fate-mapping systems that distinguish the two differentiation routes.

This work was initiated by designing genetic systems that distinguished the direct and stepwise differentiation routes for hematopoiesis. We found that Cd48-Dre specifically and constitutively marked all haematopoietic cells on the stepwise differentiation route. A combination of KitcreER, Cd48dre and Rosa26loxp-STOP-loxp-rox-loxp-ZsGreen-STOP-rox-tdTomato allowed inducible and simultaneous fate-mapping of haematopoietic stem and progenitor cells on the direct and stepwise differentiation routes.

We mapped the turnover rates and differentiation kinetics of each branch of the hematopoietic hierarchy. 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. Consistent with this, megakaryocytes generated through different routes displayed different activities in vitro and in vivo. Chemotherapy preferentially enhanced megakaryopoiesis through the direct route, whereas inflammation preferentially enhanced megakaryopoiesis through the stepwise route. In summary, our work links the differentiation route to the cellular heterogeneity of adult megakaryocytes. Alternative differentiation routes result in variable combinations of functionally distinct megakaryocyte subpopulations poised for different physiological demands.

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1021 - 分化途径决定成体巨核细胞生成的功能输出
近十年来,造血干细胞(HSC)领域的一项突破是发现了从原始造血干细胞到成熟巨核细胞的两种可供选择的分化途径:一种是通过逐步造血分级(逐步途径),另一种是直接分化(直接途径)。这就提出了一个根本性问题,即巨核细胞的两种替代分化途径在生理上的重要性。解决这一问题的主要挑战是缺乏能区分两种分化途径的命运图谱系统。这项工作的起点是设计能区分造血的直接分化途径和逐步分化途径的基因系统。我们发现,Cd48-Dre 能特异性地、组成性地标记逐步分化途径上的所有造血细胞。KitcreER、Cd48dre和Rosa26loxp-STOP-loxp-roxp-loxp-ZsGreen-STOP-rox-tdTomato的组合可诱导并同时绘制直接和逐步分化路线上造血干细胞和祖细胞的命运图谱。我们发现,在平衡状态下,巨核细胞通过两种途径产生,其动力学和数量相当。对命运图谱巨核细胞进行的单细胞 RNA 序列分析表明,直接途径和逐步途径分别产生了龛位支持巨核细胞和免疫巨核细胞,但同时也产生了血小板生成巨核细胞。与此相一致,通过不同途径生成的巨核细胞在体外和体内显示出不同的活性。化疗更倾向于通过直接途径促进巨核细胞生成,而炎症更倾向于通过逐步途径促进巨核细胞生成。总之,我们的工作将分化途径与成体巨核细胞的细胞异质性联系起来。不同的分化途径会产生不同功能的巨核细胞亚群组合,以满足不同的生理需求。
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来源期刊
Experimental hematology
Experimental hematology 医学-血液学
CiteScore
5.30
自引率
0.00%
发文量
84
审稿时长
58 days
期刊介绍: Experimental Hematology publishes new findings, methodologies, reviews and perspectives in all areas of hematology and immune cell formation on a monthly basis that may include Special Issues on particular topics of current interest. The overall goal is to report new insights into how normal blood cells are produced, how their production is normally regulated, mechanisms that contribute to hematological diseases and new approaches to their treatment. Specific topics may include relevant developmental and aging processes, stem cell biology, analyses of intrinsic and extrinsic regulatory mechanisms, in vitro behavior of primary cells, clonal tracking, molecular and omics analyses, metabolism, epigenetics, bioengineering approaches, studies in model organisms, novel clinical observations, transplantation biology and new therapeutic avenues.
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