Ex-vivo iTreg differentiation revisited: Convenient alternatives to existing strategies

被引:6
作者
Akkaya, Billur [1 ]
Holstein, Amanda H. [1 ]
Isaac, Christopher [1 ]
Maz, Mitra P. [1 ]
Glass, Deborah D. [1 ]
Shevach, Ethan M. [1 ]
Akkaya, Munir [2 ]
机构
[1] NIAID, Immunol Lab, NIH, Bldg 10, Bethesda, MD 20892 USA
[2] NIAID, Immunogenet Lab, NIH, Rockville, MD 20852 USA
基金
美国国家卫生研究院;
关键词
FACS sorting; Magnetic separation; Regulatory T cells; Foxp3; Suppression assay; REGULATORY T-CELLS; GENERATION;
D O I
10.1016/j.jim.2016.11.013
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Ex-vivo differentiation of regulatory T cells (Tregs) from naive CD4(+) T-cells has been widely used in immunological research. Isolation of a highly pure naive T cell population is the key factOr that determines the efficiency of subsequent Treg differentiation. Currently, this step relies mostly on FACS sorting, which is often costly, time consuming, and inconvenient. Alternatively, magnetic separation of T-cells can be performed; yet, available protocols fail to reach sort level purity and consequently result in low Treg differentiation efficiency. Here, we present the results of a comprehensive side-by-side comparison of various magnetic separation strategies and FACS sorting in multiple levels. Additionally, we propose a novel optimized custom made magnetic separation protocol, which not only yields sort level purity and Treg differentiation but also lowers the reagent costs up to 75% compared to the commercially available purification kits. The highly pure naive CD4(+) T-cell population obtained by this versatile method can also be used for differentiation of other T-cell subsets; therefore this protocol may have broad applications in T-cell research. Published by Elsevier B.V.
引用
收藏
页码:67 / 71
页数:5
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