Rieger Michael A, Schroeder Timm
Institute of Stem Cell Research, Helmholtz Zentrum Munchen - German Research Center for Environmental Health, Neuherberg/Munich, Germany.
Cells Tissues Organs. 2008;188(1-2):139-49. doi: 10.1159/000114540. Epub 2008 Jan 29.
Hematopoietic stem cell research has made tremendous progress over the last decades, and blood has become one of the best understood mammalian stem cell systems. The easy accessibility of hematopoietic cells, which are not tightly embedded in tissue, has supported this fast development. However, the hematopoietic system also exhibits disadvantages over other stem cell systems: the identity of individual cells is quickly lost when followed in cell culture and developmental stages cannot easily be distinguished by morphology. Therefore, difficulties to constantly analyze the fate of single cells are one reason for many open questions in hematopoiesis. So far, most findings are based on endpoint analyses of populations, consisting of heterogeneous cells in different stages of development or cell cycle. However, endpoint analyses merely reflect the result of a progressive sequence of fate decisions, whereas individual decisions, which would elucidate stem cell behavior, are not investigated. Thorough observation of the fate of individual cells and their progeny over many generations will add to a comprehensive understanding of the regulation of stem cell behavior. Here, we review current attempts of single cell analyses in hematopoiesis research and outline how time-lapse imaging and single cell tracking can contribute to approaching long-standing questions in hematopoiesis.
在过去几十年里,造血干细胞研究取得了巨大进展,血液已成为研究最为透彻的哺乳动物干细胞系统之一。造血细胞易于获取,且未紧密嵌入组织,这推动了该领域的快速发展。然而,与其他干细胞系统相比,造血系统也存在劣势:在细胞培养过程中,单个细胞的特性很快就会丧失,而且发育阶段难以通过形态学轻易区分。因此,难以持续分析单个细胞的命运是造血领域诸多未解之谜的原因之一。到目前为止,大多数研究结果基于对细胞群体的终点分析,这些细胞群体由处于不同发育阶段或细胞周期的异质细胞组成。然而,终点分析仅仅反映了一系列渐进的命运决定的结果,而那些能够阐明干细胞行为的个体决定并未得到研究。对单个细胞及其多代子代的命运进行全面观察,将有助于更全面地理解干细胞行为的调控机制。在此,我们综述了造血研究中当前单细胞分析的尝试,并概述了延时成像和单细胞追踪如何有助于解决造血领域长期存在的问题。