优化小鼠造血干细胞分离和代谢组学分析的预富集策略。

IF 2.5 4区 医学 Q2 HEMATOLOGY
Célina Nielsen , Youzhong Liu , Fleur Leguay , Hernán A. Tirado , Nicolas Dauguet , Nick van Gastel
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引用次数: 0

摘要

造血干细胞具有自我更新能力和产生所有成熟血细胞类型的能力,血细胞的产生源于造血干细胞的活性。小鼠仍是血液学研究中研究最多的物种之一,用于定义和分离小鼠造血干细胞的标记物也已确立。由于骨髓中造血干细胞的频率很低,因此在分离过程中通常会通过红细胞裂解和磁性细胞分离进行干细胞预富集,以缩短分拣时间。目前有几种预富集策略,其速度、富集程度、最终细胞产量和成本各不相同。在本研究中,我们进行了并排比较,并提供了一个决策树,帮助研究人员根据其下游应用选择小鼠造血干细胞分离的预富集策略。然后,我们结合造血干细胞代谢组学分析比较了不同的预富集技术,其中预富集的速度、产量和温度是关键因素,结果发现预富集策略的选择会显著影响检测到的代谢物数量和造血干细胞中单个代谢物的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimization of pre-enrichment strategies for mouse hematopoietic stem cell isolation and metabolomic analysis

Blood cell production arises from the activity of hematopoietic stem cells (HSCs), defined by their self-renewal capacity and ability to give rise to all mature blood cell types. The mouse remains one of the most studied species in hematological research, and markers to define and isolate mouse HSCs are well-established. Given the very low frequency of HSCs in the bone marrow, stem cell pre-enrichment by red blood cell lysis and magnetic cell separation is often performed as part of the isolation process to reduce sorting times. Several pre-enrichment strategies are available, differing in their speed, degree of enrichment, final cell yield, and cost. In the current study, we performed a side-by-side comparison and provide a decision tree to help researchers select a pre-enrichment strategy for mouse HSC isolation depending on their downstream application. We then compared different pre-enrichment techniques in combination with metabolomics analysis of HSCs, where speed, yield and temperature during pre-enrichment are crucial factors, and found that the choice of pre-enrichment strategy significantly impacts the number of metabolites detected and levels of individual metabolites in HSCs.

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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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