Farrelly Olivia, Kuri Paola, Rompolas Panteleimon
Department of Dermatology, Institute for Regenerative Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Methods Mol Biol. 2019;1879:1-14. doi: 10.1007/7651_2018_172.
Studies characterizing stem cell lineages in different organs aim to understand which cells particular progenitors can give rise to and how this process is controlled. Because the skin contains several resident stem cell populations and undergoes constant turnover, it is an ideal tissue in which to study this phenomenon. Furthermore, with the advent of two-photon microscopy techniques in combination with genetic tools for cell labeling, this question can be studied non-invasively by using live imaging. In this chapter, we describe an experimental approach that takes this technique one step further. We combine the Cre and Tet inducible genetic systems for single clone labeling and genetic manipulation in a specific stem cell population in the skin by using known drivers. Our system involves the use of gain- and loss-of-function alleles activated only in a differentially labeled population to distinguish single clones. The same region within a tissue is imaged repeatedly to document the fate and interactions of single clones with and without genetic modifications in the long term. Implementing this lineage tracing approach while documenting changes in cell behavior brought about by the genetic alterations allows both aspects to be linked. Because of the inherent flexibility of the approach, we expect it to have broad applications in studying stem cell function not only in the skin, but also in other tissues amenable to live imaging.
旨在了解特定祖细胞可分化为何种细胞以及该过程如何受到控制的研究,着重于描绘不同器官中的干细胞谱系。由于皮肤含有多个常驻干细胞群体且处于持续更新状态,因此它是研究这一现象的理想组织。此外,随着双光子显微镜技术与细胞标记基因工具的结合应用,通过实时成像可对这一问题进行非侵入性研究。在本章中,我们将介绍一种使该技术更进一步的实验方法。我们利用已知的驱动因子,将Cre和Tet诱导基因系统相结合,用于皮肤特定干细胞群体中的单克隆标记和基因操作。我们的系统涉及使用仅在差异标记群体中激活的功能获得和功能缺失等位基因来区分单克隆。对组织内的同一区域进行反复成像,以长期记录经过和未经基因改造的单克隆的命运及相互作用。在记录基因改变所引起的细胞行为变化的同时实施这种谱系追踪方法,可将两个方面联系起来。由于该方法具有内在的灵活性,我们预计它不仅在皮肤干细胞功能研究中,而且在其他适合实时成像的组织中都将有广泛应用。