Direct generation of human naive induced pluripotent stem cells from somatic cells in microfluidics

被引:69
作者
Giulitti, Stefano [1 ,2 ,3 ]
Pellegrini, Marco [3 ]
Zorzan, Irene [3 ]
Martini, Paolo [4 ]
Gagliano, Onelia [1 ,2 ]
Mutarelli, Margherita [5 ]
Ziller, Michael Johannes [6 ]
Cacchiarelli, Davide [5 ,7 ]
Romualdi, Chiara [4 ]
Elvassore, Nicola [1 ,2 ,8 ,9 ]
Martello, Graziano [3 ]
机构
[1] Univ Padua, Dept Ind Engn, Padua, Italy
[2] Venetian Inst Mol Med, Padua, Italy
[3] Univ Padua, Sch Med, Dept Mol Med, Padua, Italy
[4] Univ Padua, Dept Biol, Padua, Italy
[5] Telethon Inst Genet & Med TIGEM, Pozzuoli, Italy
[6] Max Planck Inst Psychiat, Dept Translat Psychiat, Munich, Germany
[7] Univ Naples Federico II, Dept Translat Med, Naples, Italy
[8] UCL, UCL Great Ormond St Inst Child Hlth, Stem Cell & Regenerat Med Dept, London, England
[9] ShanghaiTech Univ, SIAIS, Shanghai, Peoples R China
关键词
DIFFERENTIATION; INDUCTION; MOUSE; STATE; TRANSCRIPTION; MAINTENANCE; BLASTOCYST; EXPRESSION; CULTURE;
D O I
10.1038/s41556-018-0254-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Induced pluripotent stem cells (iPSCs) are generated via the expression of the transcription factors OCT4 (also known as POU5F1), SOX2, KLF4 and cMYC (OSKM) in somatic cells. In contrast to murine naive iPSCs, conventional human iPSCs are in a more developmentally advanced state called primed pluripotency. Here, we report that human naive iPSCs (niPSCs) can be generated directly from fewer than 1,000 primary human somatic cells, without requiring stable genetic manipulation, via the delivery of modified messenger RNAs using microfluidics. Expression of the OSKM factors in combination with NANOG for 12 days generates niPSCs that are free of transgenes, karyotypically normal and display transcriptional, epigenetic and metabolic features indicative of the naive state. Importantly, niPSCs efficiently differentiate into all three germ layers. While niPSCs can be generated at low frequency under conventional conditions, our microfluidics approach enables the robust and cost-effective production of patient-specific niPSCs for regenerative medicine applications, including disease modelling and drug screening.
引用
收藏
页码:275 / +
页数:15
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