Lima Ana C, Jung Min, Rusch Jannette, Usmani Abul, Lopes Alexandra M, Conrad Donald F
Department of Genetics, Washington University School of Medicine; Graduate Program in Areas of Basic and Applied Biology (GABBA), Abel Salazar Institute of Biomedical Sciences, University of Porto; Instituto de Investigação e Inovação em Saúde, University of Porto; IPATIMUP - Instituto de Patologia e Imunologia Molecular da Universidade do Porto.
Department of Genetics, Washington University School of Medicine.
J Vis Exp. 2017 Jul 12(125):55913. doi: 10.3791/55913.
Fluorescence-activated cell sorting (FACS) has been one of the methods of choice to isolate enriched populations of mammalian testicular germ cells. Currently, it allows the discrimination of up to 9 murine germ cell populations with high yield and purity. This high-resolution in discrimination and purification is possible due to unique changes in chromatin structure and quantity throughout spermatogenesis. These patterns can be captured by flow cytometry of male germ cells stained with fluorescent DNA-binding dyes such as Hoechst-33342 (Hoechst). Herein is a detailed description of a recently developed protocol to isolate mammalian testicular germ cells. Briefly, single cell suspensions are generated from testicular tissue by mechanical dissociation, double stained with Hoechst and propidium iodide (PI) and processed by flow cytometry. A serial gating strategy, including the selection of live cells (PI negative) with different DNA content (Hoechst intensity), is used during FACS sorting to discriminate up to 5 germ cell types. These include, with corresponding average purities (determined by microscopy evaluation): spermatogonia (66%), primary (71%) and secondary (85%) spermatocytes, and spermatids (90%), further separated into round (93%) and elongating (87%) subpopulations. Execution of the entire workflow is straightforward, allows the isolation of 4 cell types simultaneously with the appropriate FACS machine, and can be performed in less than 2 h. As reduced processing time is crucial to preserve the physiology of ex vivo cells, this method is ideal for downstream high-throughput studies of male germ cell biology. Moreover, a standardized protocol for multispecies purification of mammalian germ cells eliminates methodological sources of variables and allows a single set of reagents to be used for different animal models.
荧光激活细胞分选(FACS)一直是分离富集哺乳动物睾丸生殖细胞群体的首选方法之一。目前,它能够以高产率和高纯度区分多达9种小鼠生殖细胞群体。由于在整个精子发生过程中染色质结构和数量的独特变化,这种在区分和纯化方面的高分辨率才得以实现。这些模式可以通过用荧光DNA结合染料如Hoechst-33342(Hoechst)染色的雄性生殖细胞的流式细胞术来捕捉。本文详细描述了一种最近开发的分离哺乳动物睾丸生殖细胞的方案。简而言之,通过机械解离从睾丸组织中生成单细胞悬液,用Hoechst和碘化丙啶(PI)进行双重染色,并通过流式细胞术进行处理。在FACS分选过程中,使用一种系列门控策略,包括选择具有不同DNA含量(Hoechst强度)的活细胞(PI阴性),以区分多达5种生殖细胞类型。这些细胞类型包括,具有相应的平均纯度(通过显微镜评估确定):精原细胞(66%)、初级(71%)和次级(85%)精母细胞以及精子细胞(90%),精子细胞进一步分为圆形(93%)和伸长形(87%)亚群。整个工作流程的执行很简单,使用合适的FACS机器可以同时分离4种细胞类型,并且可以在不到2小时内完成。由于减少处理时间对于维持离体细胞的生理状态至关重要,因此该方法对于雄性生殖细胞生物学的下游高通量研究来说是理想的。此外,一种用于多物种纯化哺乳动物生殖细胞的标准化方案消除了方法学上的变量来源,并允许使用一套试剂用于不同的动物模型。