Center for Regenerative Medicine and Department of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, Florida, USA.
Cell Therapy Research Laboratories, Daiichi Sankyo, Co, Ltd, Tokyo, Japan.
J Tissue Eng Regen Med. 2022 Mar;16(3):244-253. doi: 10.1002/term.3274. Epub 2021 Dec 19.
Mesenchymal stem/stromal cell (MSC) therapy has been investigated in multiple diseases and conditions. Although the mechanisms of MSC-based therapies are not fully understood, we and others have shown interleukin 6 (IL-6) to be an important factor in MSC function. IL-6 contributes to many biological events, such as immune response, neurogenesis, and bone remodeling. In our study, we tested the feasibility of engineering MSCs by IL-6 mRNA transfection (eMSCs-IL6) and evaluated the optimal time to harvest them after transfection. We then assessed the functional characteristics of eMSCs-IL6. Quantitative real-time PCR and ELISA results have shown that mature IL-6 mRNA was efficiently transfected into MSCs using a lipofectamine based method. The IL-6 mRNA and protein overexpression peaked after 1 day of transfection and the secreted IL-6 protein was sustained for at least 6 days. A short time course experiment demonstrated that 4 h after transfection was the best time point to harvest and freeze eMSCs-IL6 for future studies. In addition, eMSCs-IL6 maintained their characteristics as defined by International Society for Cell & Gene Therapy. The immunosuppressive capacity of conditioned culture medium (CCM) from eMSCs-IL6 (CCM-IL6) was significantly enhanced compared to naïve MSCs conditioned culture medium (CCM-control). Our studies established for the first time the feasibility of efficiently generating IL-6 overexpressing MSCs which have enhanced immunosuppressive capacity. This is providing a novel approach to improve the efficacy of MSCs for potential application in regenerative medicine.
间充质干细胞(MSC)治疗已在多种疾病和病症中进行了研究。尽管基于 MSC 的治疗机制尚未完全阐明,但我们和其他人已经表明白细胞介素 6(IL-6)是 MSC 功能的重要因素。IL-6 有助于许多生物学事件,如免疫反应、神经发生和骨重塑。在我们的研究中,我们通过 IL-6 mRNA 转染(eMSCs-IL6)来测试工程 MSC 的可行性,并评估转染后收获它们的最佳时间。然后,我们评估了 eMSCs-IL6 的功能特征。定量实时 PCR 和 ELISA 结果表明,使用基于脂质体的方法可以有效地将成熟的 IL-6 mRNA 转染到 MSC 中。IL-6 mRNA 和蛋白过表达在转染后 1 天达到峰值,分泌的 IL-6 蛋白至少持续 6 天。一个短期的实验表明,转染后 4 小时是收获和冷冻 eMSCs-IL6 以备将来研究的最佳时间点。此外,eMSCs-IL6 保持了国际细胞与基因治疗学会定义的特征。与未处理的 MSC 条件培养基(CCM-control)相比,来自 eMSCs-IL6 的条件培养基(CCM-IL6)的免疫抑制能力显著增强。我们的研究首次建立了高效生成过表达 IL-6 的 MSC 的可行性,这为提高 MSC 在再生医学中的应用效果提供了一种新方法。