Barrilleaux Bonnie, Knoepfler Paul
Department of Cell Biology and Human Anatomy, School of Medicine, University of California, Davis.
J Vis Exp. 2011 Jul 24(53):2822. doi: 10.3791/2822.
Stem and tumor cell biology studies often require viral transduction of human cells with known or suspected oncogenes, raising major safety issues for laboratory personnel. Pantropic lentiviruses, such as the commonly used VSV-G pseudotype, are a valuable tool for studying gene function because they can transduce many cell types, including non-dividing cells. However, researchers may wish to avoid production and centrifugation of pantropic viruses encoding oncogenes due to higher biosafety level handling requirements and safety issues. Several potent oncogenes, including c-Myc and SV40 large T antigen, are known to enhance production of induced pluripotent stem cells (iPSC). All other known iPSC-inducing genetic changes (OCT4, SOX2, KLF4, NANOG, LIN28, and p53 loss of function) also have links to cancer, making them of relatively high safety concern as well. While these cancer-related viruses are useful in studying cellular reprogramming and pluripotency, they must be used safely. To address these biosafety issues, we demonstrate a method for transduction of human cells with ecotropic lentivirus, with additional emphasis on reduced cost and convenient handling. We have produced ecotropic lentivirus with sufficiently high titer to transduce greater than 90% of receptor-expressing human cells exposed to the virus, validating the efficacy of this approach. Lentivirus is often concentrated by ultracentrifugation; however, this process takes several hours and can produce aerosols infectious to human biomedical researchers. As an alternative, viral particles can be more safely sedimented onto cells by complexation with chondroitin sulfate and polybrene (CS/PB). This technique increases the functional viral titer up to 3-fold in cells stably expressing murine retrovirus receptor, with negligible added time and cost. Transduction of human dermal fibroblasts (HDFs) is maximally enhanced using CS/PB concentrations approximately 4-fold lower than the optimal value previously reported for cancer cell lines, suggesting that polymer concentration should be titrated for the target cell type of interest. We therefore describe the use of methylthiazolyldiphenyl-tetrazolium bromide (MTT) to assay for polymer toxicity in a new cell type. We observe equivalent viability of HDFs after viral transduction using either polymer complexation or the standard dose of polybrene (PB, 6 μg/ml), indicating minimal acute toxicity. In this protocol, we describe the use of ecotropic lentivirus for overexpression of oncogenes in human cells, reducing biosafety risks and increasing the transduction rate. We also demonstrate the use of polymer complexation to enhance transduction while avoiding aerosol-forming centrifugation of viral particles.
干细胞和肿瘤细胞生物学研究通常需要用已知或疑似致癌基因对人类细胞进行病毒转导,这给实验室人员带来了重大安全问题。泛嗜性慢病毒,如常用的VSV-G假型病毒,是研究基因功能的宝贵工具,因为它们可以转导多种细胞类型,包括非分裂细胞。然而,由于更高的生物安全水平处理要求和安全问题,研究人员可能希望避免生产和离心携带致癌基因的泛嗜性病毒。已知几种强效致癌基因,包括c-Myc和SV40大T抗原,可增强诱导多能干细胞(iPSC)的产生。所有其他已知的诱导iPSC的基因变化(OCT4、SOX2、KLF4、NANOG、LIN28和p53功能丧失)也与癌症有关,这也使它们具有较高的安全隐患。虽然这些与癌症相关的病毒在研究细胞重编程和多能性方面很有用,但必须安全使用。为了解决这些生物安全问题,我们展示了一种用嗜亲性慢病毒转导人类细胞的方法,并特别强调降低成本和便于操作。我们生产的嗜亲性慢病毒滴度足够高,能够转导超过90%暴露于该病毒的表达受体的人类细胞,验证了这种方法的有效性。慢病毒通常通过超速离心进行浓缩;然而,这个过程需要几个小时,并且会产生对人类生物医学研究人员有传染性的气溶胶。作为一种替代方法,病毒颗粒可以通过与硫酸软骨素和聚凝胺(CS/PB)复合更安全地沉淀到细胞上。在稳定表达鼠逆转录病毒受体的细胞中,这种技术可使功能性病毒滴度提高至3倍,而增加的时间和成本可忽略不计。使用比先前报道的癌细胞系最佳值低约4倍的CS/PB浓度可最大程度增强人皮肤成纤维细胞(HDF)的转导,这表明应针对感兴趣的靶细胞类型调整聚合物浓度。因此,我们描述了使用甲基噻唑基二苯基溴化四氮唑(MTT)来检测新细胞类型中聚合物的毒性。我们观察到,使用聚合物复合或标准剂量的聚凝胺(PB,6μg/ml)进行病毒转导后,HDF的活力相当,表明急性毒性最小。在本方案中,我们描述了使用嗜亲性慢病毒在人类细胞中过表达致癌基因,降低生物安全风险并提高转导率。我们还展示了使用聚合物复合来增强转导,同时避免对病毒颗粒进行形成气溶胶的离心操作。