Jones Sarah, Howl John
Research Institute in Healthcare Science, School of Applied Sciences, University of Wolverhampton, Wolverhampton, UK.
Methods Mol Biol. 2011;683:291-303. doi: 10.1007/978-1-60761-919-2_21.
The discovery of cell-penetrating peptides (CPP) has provided the scientific community with relatively small and increasingly cost-effective molecular agents that readily cross the normally impermeable cell membrane. Thus, as either inert delivery vectors or biologically active agents, CPP can be used to selectively modulate intracellular signal transduction events. Indeed, the survival of many cancer cells is associated with alterations in the function of key intracellular signalling proteins. Accordingly, CPP constructs have been developed to access intracellular target loci in both normal and transformed cells. Thus, CPP are a novel, generic class of signal transduction modulator which can be utilized to specifically induce apoptosis in tumour cells as a potential therapeutic option. However, and particularly at higher concentrations, CPP can induce non-specific membrane perturbations, thus leading to cell death by necrotic mechanisms. This chapter, therefore, focuses on methodologies for the assessment of apoptotic events, including in situ TUNEL analysis, activation of caspase-3, and the MTT assay, whilst also discussing dual Annexin V and propidium iodide staining, an assay used for the quantification of cell populations undergoing apoptosis and/or necrosis.
细胞穿透肽(CPP)的发现为科学界提供了相对较小且成本效益日益提高的分子试剂,这些试剂能够轻松穿过通常具有屏障作用的细胞膜。因此,作为惰性递送载体或生物活性剂,CPP可用于选择性调节细胞内信号转导事件。事实上,许多癌细胞的存活与关键细胞内信号蛋白功能的改变有关。相应地,已开发出CPP构建体以进入正常细胞和转化细胞中的细胞内靶位点。因此,CPP是一类新型的通用信号转导调节剂,可作为一种潜在的治疗选择用于特异性诱导肿瘤细胞凋亡。然而,特别是在较高浓度下,CPP可诱导非特异性膜扰动,从而通过坏死机制导致细胞死亡。因此,本章重点介绍评估凋亡事件的方法,包括原位TUNEL分析、caspase-3的激活和MTT测定,同时还讨论双Annexin V和碘化丙啶染色,一种用于定量经历凋亡和/或坏死的细胞群体的测定方法。