A solution for highly efficient electroporation of primary cytotoxic T lymphocytes.

IF 3.5 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Biotechnology Pub Date : 2024-03-26 DOI:10.1186/s12896-024-00839-4
Nadia Alawar, Claudia Schirra, Meltem Hohmann, Ute Becherer
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Abstract

Background: Cytotoxic T lymphocytes (CTLs) are central players in the adaptive immune response. Their functional characterization and clinical research depend on efficient and reliable transfection. Although various methods have been utilized, electroporation remains the preferred technique for transient gene over-expression. However, the efficiency of electroporation is reduced for human and mouse primary CTLs. Lonza offers kits that effectively improve plasmid DNA transfection quality. Unfortunately, the removal of key components of the cell recovery medium considerably reduced the efficiency of their kit for CTLs. Our aim was to develop a new recovery medium to be used with Lonza's Nucleofector system that would significantly enhance transfection rates.

Results: We assessed the impact of different media in which the primary CTLs were placed to recover after electroporation on cell survival, transfection rate and their ability to form an immunological synapse and to perform exocytosis. We transfected the cells with pmax-GFP and large constructs encoding for either CD81-super ecliptic pHluorin or granzyme B-pHuji. The comparison of five different media for mouse and two for human CTLs demonstrated that our new recovery medium composed of Opti-MEM-GlutaMAX supplemented with HEPES, DMSO and sodium pyruvate gave the best result in cell survival (> 50%) and transfection rate (> 30 and 20% for mouse and human cells, respectively). More importantly, the functionality of CTLs was at least twice as high as with the original Lonza recovery medium. In addition, our RM significantly improved transfection efficacy of natural killer cells that are notoriously hard to electroporate.

Conclusion: Our results show that successful transfection depends not only on the electroporation medium and pulse sequence but also on the medium applied for cell recovery. In addition, we have reduced our reliance on proprietary products by designing an effective recovery medium for both mouse and human primary CTLs and other lymphocytes that can be easily implemented by any laboratory. We expect that this recovery medium will have a significant impact on both fundamental and applied research in immunology.

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高效电穿孔原代细胞毒性 T 淋巴细胞的解决方案。
背景:细胞毒性 T 淋巴细胞(CTL细胞毒性 T 淋巴细胞(CTL)是适应性免疫反应的核心参与者。它们的功能表征和临床研究依赖于高效可靠的转染。虽然已经使用了多种方法,但电穿孔仍是瞬时基因过表达的首选技术。然而,对于人类和小鼠原代 CTL 而言,电穿孔的效率较低。龙沙提供的试剂盒能有效提高质粒 DNA 的转染质量。遗憾的是,由于去除了细胞回收培养基中的关键成分,大大降低了其试剂盒用于 CTL 的效率。我们的目标是开发一种新的恢复培养基,与龙沙的 Nucleofector 系统配合使用,以显著提高转染率:我们评估了电穿孔后将原代 CTL 放入不同的恢复培养基对细胞存活率、转染率及其形成免疫突触和进行外渗能力的影响。我们用 pmax-GFP 和编码 CD81-super ecliptic pHluorin 或 granzyme B-pHuji 的大构建体转染细胞。通过比较五种不同的小鼠 CTL 培养基和两种不同的人 CTL 培养基,我们发现由添加了 HEPES、DMSO 和丙酮酸钠的 Opti-MEM-GlutaMAX 组成的新型恢复培养基在细胞存活率(> 50%)和转染率(小鼠和人细胞分别> 30% 和 20%)方面效果最佳。更重要的是,CTL 的功能至少是原来使用的 Lonza 恢复培养基的两倍。此外,我们的 RM 还大大提高了难以电穿孔的自然杀伤细胞的转染效率:我们的研究结果表明,成功的转染不仅取决于电穿孔培养基和脉冲序列,还取决于用于细胞回收的培养基。此外,我们还设计了一种适用于小鼠和人类原代 CTL 及其他淋巴细胞的有效回收培养基,从而减少了对专利产品的依赖,而且任何实验室都能轻松使用。我们预计,这种恢复培养基将对免疫学的基础研究和应用研究产生重大影响。
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来源期刊
BMC Biotechnology
BMC Biotechnology 工程技术-生物工程与应用微生物
CiteScore
6.60
自引率
0.00%
发文量
34
审稿时长
2 months
期刊介绍: BMC Biotechnology is an open access, peer-reviewed journal that considers articles on the manipulation of biological macromolecules or organisms for use in experimental procedures, cellular and tissue engineering or in the pharmaceutical, agricultural biotechnology and allied industries.
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