RIKEN Center for Biosystems Dynamics Research (BDR), Kobe, Hyogo, 650-0047, Japan; Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Kyoto, 606-8397, Japan.
Weill Cornell, Rockefeller, Sloan Kettering Tri-Institutional MD-PhD Program, New York, NY, 10065, USA.
Biochem Biophys Res Commun. 2021 Feb 5;539:34-41. doi: 10.1016/j.bbrc.2020.12.077. Epub 2021 Jan 5.
Self-renewal and multipotency are essential functions of hematopoietic stem cells (HSCs). To maintain homeostatic hematopoiesis, functionally uniform HSCs have been thought to be an ideal cell-of-origin. Recent technological advances in the field have allowed us to analyze HSCs with single cell resolution and implicate that functional heterogeneity may exist even within the highly purified HSC compartment. However, due in part to the technical limitations of analyzing extremely rare populations and our incomplete understanding of HSC biology, neither the biological meaning of why heterogeneity exists nor the precise mechanism of how heterogeneity is determined within the HSC compartment is entirely known. Here we show the first evidence that self-renewal capacity varies with the degree of replication stress dose and results in heterogeneity within the HSC compartment. Using the Hoxb5-reporter mouse line which enables us to distinguish between long-term (LT)-HSCs and short-term (ST)-HSCs, we have found that ST-HSCs quickly lose self-renewal capacity under high stress environments but can maintain self-renewal under low stress environments for long periods of time. Critically, exogeneous Hoxb5 expression confers protection against loss of self-renewal to Hoxb5-negative HSCs and can partially alter the cell fate of ST-HSCs to that of LT-HSCs. Our results demonstrate that Hoxb5 imparts functional heterogeneity in the HSC compartment by regulating self-renewal capacity. Additionally, Hoxb5-positive HSCs may exist as fail-safe system to protect from the exhaustion of HSCs throughout an organism's lifespan.
自我更新和多能性是造血干细胞(HSCs)的基本功能。为了维持稳态造血,功能一致的 HSCs 被认为是理想的起始细胞。该领域最近的技术进步使我们能够以单细胞分辨率分析 HSCs,并表明即使在高度纯化的 HSC 区室中,功能异质性也可能存在。然而,部分由于分析极其罕见群体的技术限制以及我们对 HSC 生物学的不完全理解,功能异质性存在的生物学意义以及 HSC 区室中异质性是如何确定的精确机制尚不完全清楚。在这里,我们首次证明自我更新能力随复制应激剂量的增加而变化,并导致 HSC 区室中的异质性。使用 Hoxb5 报告小鼠系,我们能够区分长期(LT)-HSCs 和短期(ST)-HSCs,我们发现 ST-HSCs 在高应激环境下很快失去自我更新能力,但可以在低应激环境下长时间保持自我更新能力。关键的是,外源性 Hoxb5 表达赋予 Hoxb5 阴性 HSCs 免受自我更新丧失的保护作用,并可以部分改变 ST-HSCs 的细胞命运为 LT-HSCs。我们的结果表明,Hoxb5 通过调节自我更新能力赋予 HSC 区室功能异质性。此外,Hoxb5 阳性 HSCs 可能作为故障安全系统存在,以保护整个生物体寿命中 HSCs 的耗竭。