Concise Review: Application of Chemically Modified mRNA in Cell Fate Conversion and Tissue Engineering

被引:30
作者
Badieyan, Zohreh Sadat [1 ]
Evans, Todd [1 ]
机构
[1] Cornell Univ, Dept Surg, Weill Cornell Med, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
Nucleic acid therapy; Cell programming and reprogramming; Differentiation; iPSCs; Nanoparticles; Regenerative medicine; PLURIPOTENT STEM-CELLS; IN-VITRO; EFFICIENT GENERATION; HUMAN FIBROBLASTS; PROGENITOR CELLS; ENCODING BMP-2; SOMATIC-CELLS; GENE-TRANSFER; SENDAI-VIRUS; DELIVERY;
D O I
10.1002/sctm.18-0259
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Chemically modified RNA (cmRNA) has potential as a safe and efficient tool for nucleic acid-based therapies and regenerative medicine. Modifications in the chemistry of mRNA can enhance stability, reduce immunogenicity, and thus facilitate mRNA-based nucleic acid therapy, which eliminates risk of insertional mutagenesis. In addition to these valuable advantages, the mRNA-based method showed significantly higher efficacy for reprogramming somatic cells to pluripotency compared with DNA- or protein-based methods. These findings suggest cmRNA can provide a powerful and safe tool for cell programming and reprogramming. Delivery methods, particularly using lipid nanoparticles, provide strategies for cell and organ-specific targeting. The present study comprehensively compares studies that have used cmRNAs for cell fate conversion and tissue engineering. The information should be useful for investigators looking to choose the most efficient and straightforward cmRNA-based strategy and protocol for tissue engineering and regenerative medicine research.
引用
收藏
页码:833 / 843
页数:11
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