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使用流式细胞术定量分析活细胞中的细胞凋亡和坏死。

Quantitative Analysis of Apoptosis and Necrosis in Live Cells Using Flow Cytometry.

机构信息

Cancer Research Program-1, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.

Manipal Academy of Higher Education , Manipal, Karnataka, India.

出版信息

Methods Mol Biol. 2022;2543:57-69. doi: 10.1007/978-1-0716-2553-8_6.

Abstract

Apoptosis and necrosis are the two sides of the cell death penumbra. Apoptosis is a well-studied model of cell death wherein the cell destroys itself employing a predefined form of active signaling without the release of soluble cytoplasmic contents to the external environment. Compared to apoptosis, necrosis is a nonspecific form of sudden cell death in response to an invasive external stimulus which in turn is devoid of active programmed intracellular signaling leading to the sudden release of the soluble cellular contents consequent to the rupture of the cell membrane. This fundamental difference between apoptosis and necrosis made us believe that the former is the safe form of cell death and the latter is an undesirable one which often elicits an inflammatory response to the adjacent cells. Recent studies have shown that necrosis also involves a few defined cellular and complex biochemical events similar to apoptosis rendering it difficult to distinguish these two events at the single-cell level using the currently used popular assays.Here we provide a newly described detailed methodology encompassing cell system development along with a multiparametric flow cytometry-based approach to discriminate apoptotic cells from necrotic cells using a stable cell line expressing genetically encoded probe for detecting caspase activation and DsRed targeted at the mitochondria.

摘要

细胞凋亡和坏死是细胞死亡边缘的两个方面。细胞凋亡是细胞死亡的一种研究充分的模型,其中细胞通过预先设定的主动信号方式自我破坏,而不会将可溶性细胞质内容物释放到外部环境中。与细胞凋亡相比,坏死是一种对侵入性外部刺激的非特异性突然细胞死亡形式,而这种刺激反过来又缺乏主动的程序性细胞内信号传导,导致细胞膜破裂后可溶性细胞内容物的突然释放。细胞凋亡和坏死之间的这种根本区别使我们相信前者是安全的细胞死亡形式,而后者是一种不理想的形式,通常会引发邻近细胞的炎症反应。最近的研究表明,坏死也涉及到一些类似于细胞凋亡的明确的细胞和复杂的生化事件,这使得使用目前常用的流行检测方法在单细胞水平上很难区分这两种事件。在这里,我们提供了一种新描述的详细方法,包括细胞系统的开发以及基于多参数流式细胞术的方法,使用表达基因编码探针检测半胱天冬酶激活和靶向线粒体的 DsRed 的稳定细胞系来区分凋亡细胞和坏死细胞。

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