Department of Mathematical Sciences, University of Nevada, Las Vegas, NV, USA.
Blood. 2011 Apr 28;117(17):4460-6. doi: 10.1182/blood-2010-08-303537. Epub 2011 Feb 22.
Hematopoietic stem cells (HSCs) replicate (self-renew) to create 2 daughter cells with capabilities equivalent to their parent, as well as differentiate, and thus can both maintain and restore blood cell production. Cell labeling with division-sensitive markers and competitive transplantation studies have been used to estimate the replication rate of murine HSCs in vivo. However, these methods are not feasible in humans and surrogate assays are required. In this report, we analyze the changing ratio with age of maternal/paternal X-chromosome phenotypes in blood cells from females and infer that human HSCs replicate on average once every 40 weeks (range, 25-50 weeks). We then confirm this estimate with 2 independent approaches, use the estimate to simulate human hematopoiesis, and show that the simulations accurately reproduce marrow transplantation data. Our simulations also provide evidence that the number of human HSCs increases from birth until adolescence and then plateaus, and that the ratio of contributing to quiescent HSCs in humans significantly differs from mouse. In addition, they suggest that human marrow failure, such as the marrow failure that occurs after umbilical cord blood transplantation and with aplastic anemia, results from insufficient numbers of early progenitor cells, and not the absence of HSCs.
造血干细胞(HSCs)通过自我复制产生 2 个具有与其亲本相同能力的子细胞,并进行分化,从而既能维持又能恢复血细胞的产生。细胞标记有丝分裂敏感标记物和竞争移植研究已被用于估计体内鼠类 HSCs 的复制率。然而,这些方法在人类中不可行,需要替代测定法。在本报告中,我们分析了女性血液细胞中母系/父系 X 染色体表型随年龄变化的比例,并推断人类 HSCs 平均每 40 周(范围 25-50 周)复制一次。然后,我们用两种独立的方法证实了这一估计值,使用该估计值模拟人类造血,并表明模拟准确地再现了骨髓移植数据。我们的模拟还提供了证据表明,人类 HSCs 的数量从出生到青春期增加,然后达到稳定,并且人类中对静止 HSCs 的贡献比例与小鼠有显著差异。此外,它们表明,人类骨髓衰竭,如脐带血移植后和再生障碍性贫血发生的骨髓衰竭,是由于早期祖细胞数量不足,而不是 HSCs 缺失所致。