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定量单细胞方法在干细胞研究中的应用。

Quantitative single-cell approaches to stem cell research.

机构信息

Department of Biosystems Science and Engineering, ETH Zurich, 4058 Basel, Switzerland.

Department of Biosystems Science and Engineering, ETH Zurich, 4058 Basel, Switzerland.

出版信息

Cell Stem Cell. 2014 Nov 6;15(5):546-58. doi: 10.1016/j.stem.2014.10.015.

Abstract

Understanding the molecular control of cell fates is central to stem cell research. Such insight requires quantification of molecular and cellular behavior at the single-cell level. Recent advances now permit high-throughput molecular readouts from single cells as well as continuous, noninvasive observation of cell behavior over time. Here, we review current state-of-the-art approaches used to query stem cell fate at the single-cell level, including advances in lineage tracing, time-lapse imaging, and molecular profiling. We also offer our perspective on the advantages and drawbacks of available approaches, key technical limitations, considerations for data interpretation, and future innovation.

摘要

理解细胞命运的分子控制是干细胞研究的核心。这种洞察力需要在单细胞水平上定量分子和细胞行为。最近的进展现在允许从单细胞中进行高通量的分子读出,以及随着时间的推移对细胞行为进行连续的、非侵入性的观察。在这里,我们回顾了目前用于在单细胞水平上查询干细胞命运的最先进方法,包括谱系追踪、延时成像和分子分析方面的进展。我们还提供了对现有方法的优缺点、关键技术限制、数据解释的考虑因素以及未来创新的看法。

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