Department of Biology, York Biomedical Research Institute, University of York, York, United Kingdom.
Blood. 2023 Aug 10;142(6):543-552. doi: 10.1182/blood.2022017864.
One of the most challenging aspects of stem cell research is the reliance on retrospective assays for ascribing function. This is especially problematic for hematopoietic stem cell (HSC) research in which the current functional assay that formally establishes its HSC identity involves long-term serial transplantation assays that necessitate the destruction of the initial cell state many months before knowing that it was, in fact, an HSC. In combination with the explosion of equally destructive single-cell molecular assays, the paradox facing researchers is how to determine the molecular state of a functional HSC when you cannot concomitantly assess its functional and molecular properties. In this review, we will give a historical overview of the functional and molecular assays in the field, identify new tools that combine molecular and functional readouts in populations of HSCs, and imagine the next generation of computational and molecular profiling tools that may help us better link cell function with molecular state.
干细胞研究中最具挑战性的方面之一是依赖回顾性分析来赋予功能。这对于造血干细胞(HSC)研究来说尤其成问题,因为目前正式确定其 HSC 身份的功能检测需要进行长期的连续移植检测,这需要在知道其实际上是 HSC 之前的数月内破坏初始细胞状态。再加上同样具有破坏性的单细胞分子检测的爆炸式增长,研究人员面临的悖论是,当您不能同时评估功能 HSC 的功能和分子特性时,如何确定其分子状态。在这篇综述中,我们将回顾该领域的功能和分子检测方法,确定可在 HSC 群体中结合分子和功能读数的新工具,并设想下一代计算和分子分析工具,以帮助我们更好地将细胞功能与分子状态联系起来。