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优化的逆转录病毒工具包,用于过表达和遗传干扰原代淋巴细胞。

An optimized retroviral toolbox for overexpression and genetic perturbation of primary lymphocytes.

机构信息

Department of Experimental Immunology, Amsterdam institute for Infection and Immunity, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam 1105 AZ, the Netherlands.

Division of Infectious Diseases and Center of Experimental and Molecular Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam 1105 AZ, the Netherlands.

出版信息

Biol Open. 2022 Feb 15;11(2). doi: 10.1242/bio.059032. Epub 2022 Mar 1.

Abstract

Genetic manipulation of primary lymphocytes is crucial for both clinical purposes and fundamental research. Despite their broad use, we encountered a paucity of data on systematic comparison and optimization of retroviral vectors, the workhorses of genetic modification of primary lymphocytes. Here, we report the construction and validation of a versatile range of retroviral expression vectors. These vectors can be used for the knockdown or overexpression of genes of interest in primary human and murine lymphocytes, in combination with a wide choice of selection and reporter strategies. By streamlining the vector backbone and insert design, these publicly available vectors allow easy interchangeability of the independent building blocks, such as different promoters, fluorescent proteins, surface markers and antibiotic resistance cassettes. We validated these vectors and tested the optimal promoters for in vitro and in vivo overexpression and knockdown of the murine T cell antigen receptor. By publicly sharing these vectors and the data on their optimization, we aim to facilitate genetic modification of primary lymphocytes for researchers entering this field.

摘要

基因操控原发性淋巴细胞对于临床和基础研究都至关重要。尽管它们被广泛应用,但我们发现缺乏对逆转录病毒载体(基因修饰原发性淋巴细胞的主要工具)进行系统比较和优化的数据。在这里,我们报告了一系列多功能逆转录病毒表达载体的构建和验证。这些载体可用于敲低或过表达原代人源和鼠源淋巴细胞中的目的基因,并与广泛的选择和报告策略相结合。通过简化载体骨架和插入设计,这些公开可用的载体允许独立构建块(如不同的启动子、荧光蛋白、表面标记物和抗生素抗性盒)的轻松互换。我们验证了这些载体,并测试了最佳启动子,用于在体外和体内过表达和敲低鼠 T 细胞抗原受体。通过公开共享这些载体及其优化数据,我们旨在为进入该领域的研究人员提供便利,以促进对原发性淋巴细胞的基因修饰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d104/8905627/90fd0bb94173/biolopen-11-059032-g1.jpg

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