INSERM U768, Université Paris-Descartes, Faculté de Médecine René Descartes, Paris, France.
Blood Cells Mol Dis. 2011 Jun 15;47(1):72-8. doi: 10.1016/j.bcmd.2011.04.001. Epub 2011 Apr 29.
An important proof of principle has been achieved with the development of an in vitro T-cell differentiation assay based on the coculture of hematopoietic progenitors with the OP9-Delta1 stromal cell line. The original murine T cell differentiation assay has since been adapted for human T-cell differentiation, however with lower efficiency. The choice of both medium and cytokines is crucial in this assay, therefore our work has been focused on these two factors. The use of freshly reconstituted medium, the optimization of interleukine-7 (IL-7) concentration, and the addition of stem cell factor (SCF) have allowed to improve the proliferation of progenitors and T-cell precursors as well as the yield of double positive CD4+CD8+ T cells, and mature γδ and αβ T cells. These optimizations make the OP9-Delta1 system sensitive enough to perform both quantitative and qualitative assays with various type of progenitors, including those transduced by a retroviral vector. The improved OP9-Delta1 assay therefore constitutes an extremely useful test for basic research purposes and for translational medicine.
已经通过开发基于造血祖细胞与 OP9-Delta1 基质细胞系共培养的体外 T 细胞分化测定法实现了一个重要的原理证明。此后,已经对原始的鼠 T 细胞分化测定法进行了适应,以用于人类 T 细胞分化,但效率较低。在该测定法中,培养基和细胞因子的选择至关重要,因此我们的工作重点一直放在这两个因素上。使用新重建的培养基、优化白细胞介素 7(IL-7)浓度以及添加干细胞因子(SCF),使得祖细胞和 T 细胞前体的增殖以及双阳性 CD4+CD8+T 细胞和成熟的γδ和αβT 细胞的产量得到了改善。这些优化使 OP9-Delta1 系统足够灵敏,可用于各种类型的祖细胞进行定量和定性测定,包括那些经逆转录病毒载体转导的祖细胞。因此,改良的 OP9-Delta1 测定法构成了基础研究和转化医学的极其有用的测试。