Schmachtel Tessa, Bonig Halvard, Rieger Michael A
Department of Medicine, Hematology/Oncology, Goethe University Hospital, 60590 Frankfurt, Germany.
Institute for Transfusion Medicine and Immunohematology, Goethe University Frankfurt, 60528 Frankfurt am Main, Germany.
Int J Mol Sci. 2025 Aug 28;26(17):8381. doi: 10.3390/ijms26178381.
The existing heterogeneity of the human hematopoietic stem cell (HSC) compartment imposes significant challenges in understanding their physiology and molecular constitution. The hematopoietic system is hierarchically organized, with HSCs at the apex, responsible for maintaining homeostasis by ensuring a life-long supply of blood cells. HSCs are highly potent but rare, making their pure isolation challenging. To address this, flow-cytometry-based methods are commonly used to isolate HSCs, bridging the gap between surface marker expression and understanding their functional and molecular properties. However, detailed methodology papers providing practical guidance for the prospective isolation of distinct human hematopoietic stem and progenitor cell (HSPC) populations are rare, hindering reproducible applications across different research groups. Here, we present a comprehensive protocol for isolating multipotent long-term repopulating HSCs (LT-HSCs) and define multipotent progenitor populations (MPPs) from human mobilized peripheral blood (mPB) after leukapheresis using fluorescence-activated cell sorting (FACS). By highlighting the workflow, outlining critical considerations and emphasizing recent advancements in the field, we provide an extensive overview of FACS-based human HSC isolation. This facilitates the enrichment of these rare cells for downstream analysis and enables researchers to improve our understanding of the heterogeneity within the HSC compartment.
人类造血干细胞(HSC)区室现有的异质性给理解其生理学和分子构成带来了重大挑战。造血系统呈层级组织,HSC处于顶层,通过确保终身供应血细胞来维持体内平衡。HSC效力强大但数量稀少,使其纯分离具有挑战性。为解决这一问题,基于流式细胞术的方法通常用于分离HSC,弥合了表面标志物表达与理解其功能和分子特性之间的差距。然而,为前瞻性分离不同的人类造血干细胞和祖细胞(HSPC)群体提供实用指导的详细方法学论文很少,这阻碍了不同研究组之间的可重复应用。在此,我们提出了一种用于分离多能长期重建造血干细胞(LT-HSC)的综合方案,并使用荧光激活细胞分选(FACS)从白细胞分离术后的人类动员外周血(mPB)中定义多能祖细胞群体(MPP)。通过突出工作流程、概述关键注意事项并强调该领域的最新进展,我们提供了基于FACS的人类HSC分离的广泛概述。这有助于富集这些稀有细胞用于下游分析,并使研究人员能够增进我们对HSC区室异质性的理解。