Suppr超能文献

基于快速和敏感慢病毒载体的条件基因表达检测方法,用于监测和定量细胞融合活性。

Rapid and sensitive lentivirus vector-based conditional gene expression assay to monitor and quantify cell fusion activity.

机构信息

Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

PLoS One. 2010 Jun 3;5(6):e10954. doi: 10.1371/journal.pone.0010954.

Abstract

Cell-to-cell fusion is involved in multiple fundamental biological processes. Prominent examples include osteoclast and giant cell formation, fertilization and skeletal myogenesis which involve macrophage, sperm-egg and myoblast fusion, respectively. Indeed, the importance of cell fusion is underscored by the wide range of homeostatic as well as pathologic processes in which it plays a key role. Therefore, rapid and sensitive systems to trace and measure cell fusion events in various experimental systems are in demand. Here, we introduce a bipartite cell fusion monitoring system based on a genetic switch responsive to the site-specific recombinase FLP. To allow flexible deployment in both dividing as well as non-dividing cell populations, inducer and reporter modules were incorporated in lentivirus vector particles. Moreover, the recombinase-inducible transcription units were designed in such a way as to minimize basal activity and chromosomal position effects in the "off" and "on" states, respectively. The lentivirus vector-based conditional gene expression assay was validated in primary human mesenchymal stem cells and in a differentiation model based on muscle progenitor cells from a Duchenne muscular dystrophy patient using reporter genes compatible with live- and single-cell imaging and with whole population measurements. Using the skeletal muscle cell differentiation model, we showed that the new assay displays low background activity, a 2-log dynamic range, high sensitivity and is amenable to the investigation of cell fusion kinetics. The utility of the bipartite cell fusion monitoring system was underscored by a study on the impact of drug- and RNAi-mediated p38 MAPK inhibition on human myocyte differentiation. Finally, building on the capacity of lentivirus vectors to readily generate transgenic animals the present FLP-inducible system should be adaptable, alone or together with Cre/loxP-based assays, to cell lineage tracing and conditional gene manipulation studies in vivo.

摘要

细胞融合参与多种基本的生物学过程。突出的例子包括破骨细胞和巨细胞的形成、受精和骨骼肌肉发生,分别涉及巨噬细胞、精子-卵子和肌母细胞的融合。事实上,细胞融合的重要性体现在广泛的稳态和病理过程中,它在这些过程中起着关键作用。因此,需要快速和敏感的系统来追踪和测量各种实验系统中的细胞融合事件。在这里,我们介绍了一种基于对位点特异性重组酶 FLP 有反应的二部分细胞融合监测系统。为了允许在分裂和非分裂细胞群体中灵活部署,诱导剂和报告模块被整合到慢病毒载体颗粒中。此外,重组酶诱导的转录单元被设计成分别在“关闭”和“打开”状态下最小化基础活性和染色体位置效应。基于慢病毒载体的条件基因表达测定法在原代人骨髓间充质干细胞和基于杜氏肌营养不良症患者肌肉祖细胞的分化模型中得到了验证,使用与活细胞和单细胞成像以及全群体测量兼容的报告基因。使用骨骼肌细胞分化模型,我们表明新测定法具有低背景活性、2 个对数动态范围、高灵敏度,并且适用于研究细胞融合动力学。药物和 RNAi 介导的 p38 MAPK 抑制对人肌细胞分化影响的研究突出了二部分细胞融合监测系统的实用性。最后,基于慢病毒载体易于生成转基因动物的能力,本 FLP 诱导系统应该是可适应的,单独或与 Cre/loxP 为基础的测定一起,用于体内细胞谱系追踪和条件基因操作研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c72d/2880594/4f044f10be77/pone.0010954.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验