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A microRNA-Based System for Selecting and Maintaining the Pluripotent State in Human Induced Pluripotent Stem Cells
被引:23
|作者:
Di Stefano, Bruno
[1
,2
]
Maffioletti, Sara Martina
[1
]
Gentner, Bernhard
[3
,4
]
Ungaro, Federica
[1
]
Schira, Giulia
[3
]
Naldini, Luigi
[3
,4
]
Broccoli, Vania
[1
]
机构:
[1] Ist Sci San Raffaele, Stem Cells & Neurogenesis Unit, Div Neurosci, I-20132 Milan, Italy
[2] Fdn Ist Ricovero & Cura Carattere Sci Policlin Sa, Pavia, Italy
[3] San Raffaele Telethon Inst Gene Therapy, Milan, Italy
[4] Univ Vita Salute San Raffaele, Milan, Italy
来源:
关键词:
microRNA;
Induced pluripotent stem cells;
Genetic reprogramming;
Let7a;
Lin28;
Parkinson's disease;
Rett syndrome;
TRANSGENE EXPRESSION;
ENDOGENOUS MICRORNA;
GENERATION;
DIFFERENTIATION;
FIBROBLASTS;
D O I:
10.1002/stem.726
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
Induced pluripotent stem cell (iPSC) technology has provided researchers with a unique tool to derive disease-specific stem cells for the study and possible treatment of degenerative disorders with autologous cells. The low efficiency and heterogeneous nature of reprogramming is a major impediment to the generation of personalized iPSC lines. Here, we report the generation of a lentiviral system based on a microRNA-regulated transgene that enables for the efficient selection of mouse and human pluripotent cells. This system relies on the differential expression pattern of the mature form of microRNA let7a in pluripotent versus committed or differentiated cells. We generated microRNA responsive green fluorescent protein and Neo reporters for specific labeling and active selection of the pluripotent cells in any culture condition. We used this system to establish Rett syndrome and Parkinson's disease human iPSCs. The presented selection procedure represents a straightforward and powerful tool for facilitating the derivation of patient-specific iPSCs. STEM CELLS 2011;29:1684-1695
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页码:1684 / 1695
页数:12
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