James W Jacobberger, R Michael Sramkoski, Tammy Stefan, Chris Bray, C Bruce Bagwell
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引用次数: 0
Abstract
This chapter was originally written in 2011. The idea was to give some history of cell cycle analysis before and after flow cytometry became widely accessible; provide references to educational material for single parameter DNA content analysis, introduce and discuss multiparameter cell cycle analysis in a methodological style, and in a casual style, discuss aspects of the work over the last 40years that we have given thought, performing some experiments, but didn't publish. It feels like there is a linear progression that moves from counting cells for growth curves, to counting labeled mitotic cells by autoradiography, to DNA content analysis, to cell cycle states defined by immunofluorescence plus DNA content analysis, to extraction of cell cycle expression profiles, and finally to probability state modeling, which should be the "right" way to analyze cytometric cell cycle data. This is the sense of this chapter. In 2023, we have updated it, but the exciting, expansive aspects brought about by spectral and mass cytometry are still young and developing, and thus have not been vetted, reviewed, and presented in mature form.
本章最初写于 2011 年。我们的想法是介绍流式细胞仪普及前后细胞周期分析的一些历史;提供单参数 DNA 含量分析教材的参考资料,以方法论的风格介绍和讨论多参数细胞周期分析,并以随意的风格讨论我们在过去 40 年中思考过、做过一些实验但没有发表的工作。从计数细胞以绘制生长曲线,到通过自显影计数标记的有丝分裂细胞,再到 DNA 含量分析,再到通过免疫荧光和 DNA 含量分析确定细胞周期状态,再到提取细胞周期表达谱,最后到概率状态建模(这应该是分析细胞周期数据的 "正确 "方法),感觉就像一个线性发展过程。这就是本章的意义所在。2023 年,我们对其进行了更新,但光谱和质量细胞计量法所带来的令人兴奋的、广阔的方面仍处于年轻和发展阶段,因此尚未经过审核、审查和以成熟的形式呈现。
期刊介绍:
For over fifty years, Methods in Cell Biology has helped researchers answer the question "What method should I use to study this cell biology problem?" Edited by leaders in the field, each thematic volume provides proven, state-of-art techniques, along with relevant historical background and theory, to aid researchers in efficient design and effective implementation of experimental methodologies. Over its many years of publication, Methods in Cell Biology has built up a deep library of biological methods to study model developmental organisms, organelles and cell systems, as well as comprehensive coverage of microscopy and other analytical approaches.