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Lineage tracing of murine adult hematopoietic stem cells reveals active contribution to steady-state hematopoiesis

机译:小鼠成年造血干细胞的谱系追踪揭示了对稳态造血的积极作用

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摘要

Characterization of hematopoietic stem cells (HSCs) has advanced largely owing to transplantation assays, in which the developmental potential of HSCs is assessed generally in nonhomeostatic conditions. These studies established that adult HSCs extensively contribute to multilineage hematopoietic regeneration upon transplantation. On the contrary, recent studies performing lineage tracing of HSCs under homeostatic conditions have shown that adult HSCs may contribute far less to steady-state hematopoiesis than would be anticipated based on transplantation assays. Here, we used 2 independent HSC-lineage–tracing models to examine the contribution of adult HSCs to steady-state hematopoiesis. We show that adult HSCs contribute robustly to steady-state hematopoiesis, exhibiting faster efflux toward the myeloid lineages compared with lymphoid lineages. Platelets were robustly labeled by HSCs, reaching the same level of labeling as HSCs by 1 year of chase. Our results support the view that adult HSCs contribute to the continuous influx of blood cells during steady-state hematopoiesis.
机译:造血干细胞(HSC)的表征已大大提高,这归功于移植测定法,其中通常在非稳态条件下评估HSC的发育潜力。这些研究确定了成年HSC在移植后广泛地促进了多系造血再生。相反,最近在稳态条件下对HSC进行谱系追踪的研究表明,成年HSC对稳态造血的贡献远小于基于移植检测的预期。在这里,我们使用2个独立的HSC谱系追踪模型来检查成人HSC对稳态造血功能的贡献。我们显示,成年HSCs对稳态造血功能做出有力贡献,与淋巴样谱系相比,向髓样谱系表现出更快的外排。血小板被HSCs强力标记,被追踪1年达到与HSCs相同的标记水平。我们的结果支持这样的观点,即成年HSC在稳态造血过程中有助于持续流入血细胞。

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