Wang Irving E, Wagner Daniel E, Reddien Peter W
Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Methods Mol Biol. 2018;1774:479-495. doi: 10.1007/978-1-4939-7802-1_20.
Stem cells, which both self-renew and produce differentiated progeny, represent fundamental biological units for the development, growth, maintenance, and regeneration of adult tissues. Characterization of stem cell lineage potential can be accomplished with clonal assays that interrogate stem cell output at the single-cell level. Here we present two methods for clonal analysis of individual proliferative cells (neoblasts) in the planarian Schmidtea mediterranea. The first method utilizes "subtotal" gamma irradiation to study rare surviving neoblasts and their clonal descendants in their native environment. The second method utilizes a fluorescent-activated cell sorting (FACS) strategy to obtain neoblast-enriched cell fractions, followed by single-cell transplantation into lethally irradiated hosts. Together, these methods provide a framework for generation and analysis of stem cell-derived clones in planarians.
干细胞既能自我更新又能产生分化后代,是成体组织发育、生长、维持和再生的基本生物学单位。干细胞谱系潜能的表征可以通过在单细胞水平上研究干细胞输出的克隆分析来完成。本文介绍了两种对地中海涡虫中单个增殖细胞(新生细胞)进行克隆分析的方法。第一种方法利用“部分”伽马射线照射来研究在其原生环境中罕见存活的新生细胞及其克隆后代。第二种方法利用荧光激活细胞分选(FACS)策略获得富含新生细胞的细胞组分,然后将单细胞移植到接受致死剂量照射的宿主体内。这些方法共同为涡虫中干细胞衍生克隆的产生和分析提供了一个框架。