Biological Sciences, Department of Immunology, Sunnybrook Research Institute, University of Toronto, Toronto, ON, Canada.
Methods Mol Biol. 2022;2421:243-265. doi: 10.1007/978-1-0716-1944-5_17.
Fetal thymic organ culture (FTOC) provides a method for analyzing T cell development in a physiological context outside the animal. This technique enables studies of genetically altered mice that are embryonic or neonatal lethal, in addition to bypassing the complication of migration of successive waves of T cells out of the thymus. The hanging drop method involves depletion of thymocytes from host lobes using deoxyguanosine, followed by reconstitution with hematopoietic progenitors. This method has become standard for analysis of fetal liver precursors, bone marrow precursors, and early thymocytes. However, difficulties are encountered in the analysis of γδ T cell precursors using this method. We have developed a modification of FTOC in which partial depletion of hematopoietic precursors by shortened deoxyguanosine treatment, coupled with the use of TCRδ-deficient host lobes, enables engraftment and development of fetal γδTCR+ thymocytes. This method allows comparisons of development and functional differentiation of γδ T cell precursors between cells of different genotypes or treatments, in the context of a permissive thymic microenvironment.
胎胸腺器官培养(FTOC)提供了一种在动物体外的生理环境下分析 T 细胞发育的方法。这项技术可以研究胚胎或新生致死的基因改变的老鼠,此外还可以避免连续波 T 细胞从胸腺中迁移的复杂性。悬滴法涉及使用脱氧鸟苷从宿主叶中耗尽胸腺细胞,然后用造血祖细胞重建。这种方法已成为分析胎肝前体、骨髓前体和早期胸腺细胞的标准方法。然而,在使用这种方法分析 γδ T 细胞前体时会遇到困难。我们已经开发了一种 FTOC 的改良方法,其中通过缩短脱氧鸟苷处理来部分耗尽造血前体,同时使用 TCRδ 缺陷的宿主叶,能够使胎γδTCR+胸腺细胞植入和发育。这种方法允许在允许的胸腺微环境中,对不同基因型或处理的细胞的 γδ T 细胞前体的发育和功能分化进行比较。