Development and evaluation of IL-6 overexpressing mesenchymal stem cells (MSCs)

被引:6
|
作者
Huang, Peng [1 ,2 ]
Zhang, Cuiping [1 ,2 ]
Delawary, Mina [3 ]
Korchak, Jennifer A. [1 ,2 ]
Suda, Koji [3 ]
Zubair, Abba C. [1 ,2 ]
机构
[1] Mayo Clin, Ctr Regenerat Med, Jacksonville, FL 32224 USA
[2] Mayo Clin, Dept Lab Med & Pathol, Jacksonville, FL 32224 USA
[3] Daiichi Sankyo Co Ltd, Cell Therapy Res Labs, Tokyo, Japan
关键词
interleukin; 6; mesenchymal stem cells; mRNA engineering; regenerative medicine; MESSENGER-RNA; INTERLEUKIN-6; GENE; CYTOKINE; DELIVERY; THERAPY;
D O I
10.1002/term.3274
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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 naive 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.
引用
收藏
页码:244 / 253
页数:10
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