Derivation of T Cells In Vitro from Mouse Embryonic Stem Cells

被引:2
|
作者
Kucerova-Levisohn, Martina [1 ,2 ]
Lovett, Jordana [1 ,2 ]
Lahiji, Armin [1 ,2 ]
Holmes, Roxanne [3 ]
Zuniga-Pfluecker, Juan Carlos [3 ]
Ortiz, Benjamin D. [1 ,2 ]
机构
[1] CUNY Hunter Coll, Dept Biol Sci, New York, NY 10021 USA
[2] CUNY, Grad Ctr, New York, NY 10016 USA
[3] Univ Toronto, Dept Immunol, Sunnybrook Res Inst, Toronto, ON M5S 1A1, Canada
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2014年 / 92期
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
LOCUS-CONTROL REGION; TCR-ALPHA GENE; GENERATION; PROGENITORS; INDUCTION; CULTURE;
D O I
10.3791/52119
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The OP9/OP9-DL1 co-culture system has become a well-established method for deriving differentiated blood cell types from embryonic and hematopoietic progenitors of both mouse and human origin. It is now used to address a growing variety of complex genetic, cellular and molecular questions related to hematopoiesis, and is at the cutting edge of efforts to translate these basic findings to therapeutic applications. The procedures are straightforward and routinely yield robust results. However, achieving successful hematopoietic differentiation in vitro requires special attention to the details of reagent and cell culture maintenance. Furthermore, the protocol features technique sensitive steps that, while not difficult, take care and practice to master. Here we focus on the procedures for differentiation of T lymphocytes from mouse embryonic stem cells (mESC). We provide a detailed protocol with discussions of the critical steps and parameters that enable reproducibly robust cellular differentiation in vitro. It is in the interest of the field to consider wider adoption of this technology, as it has the potential to reduce animal use, lower the cost and shorten the timelines of both basic and translational experimentation.
引用
收藏
页数:11
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