Department of Biotechnology, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul, 120-749, Republic of Korea.
Arch Pharm Res. 2014 Jan;37(1):107-19. doi: 10.1007/s12272-013-0287-z. Epub 2013 Nov 13.
Nonviral delivery is a promising strategy for cellular reprogramming to produce desired cell types from undifferentiated stem cells or terminally differentiated somatic cells. Nonviral delivery of genes (DNA, RNA), proteins, or peptides has the potential to reprogram somatic cells to pluripotent stem cells or other lineage cells, and to promote the differentiation of stem cells to specific lineages. Various delivery carriers (cationic polymers, lipids, scaffolds, transposons, cell-penetrating peptides), cargos (episomal plasmids, minicircle DNA, small interfering RNAs, microRNAs, proteins, peptides), and method (electroporation) have been reported. In this article, we review recent advances in nonviral delivery approaches for reprogramming cells to pluripotency or lineage specification.
非病毒递送是一种有前途的策略,用于细胞重编程,从未分化的干细胞或终末分化的体细胞产生所需的细胞类型。基因(DNA、RNA)、蛋白质或肽的非病毒递送有可能将体细胞重编程为多能干细胞或其他谱系细胞,并促进干细胞向特定谱系的分化。各种递送载体(阳离子聚合物、脂质、支架、转座子、细胞穿透肽)、载体(附加体质粒、微环 DNA、小干扰 RNA、microRNA、蛋白质、肽)和方法(电穿孔)已经被报道。在本文中,我们综述了用于将细胞重编程为多能性或谱系特异性的非病毒递送方法的最新进展。