Jenkinson E J, Anderson G, Owen J J
Department of Anatomy, Medical School, University of Birmingham, United Kingdom.
J Exp Med. 1992 Sep 1;176(3):845-53. doi: 10.1084/jem.176.3.845.
We describe an in vitro system in which positive selection of developing T cells takes place on defined stromal cell preparations, which include major histocompatibility complex class II+ epithelial cells but exclude cells of bone marrow origin. In this system, maturation of double-positive T cell receptor negative (TCR-), CD4+8+ thymocytes into single-positive TCR+, CD4+ and CD8+ cells takes place together with the development of functional competence. As in vivo, this maturation is associated with the upregulation of TCR levels as cells progress from double-positive to single-positive status. We also show that class II+ epithelial cells in these cultures are less efficient than dendritic cells in mediating the deletion (negative selection) of V beta 8+ cells by the superantigen staphylococcal enterotoxin B. For the first time, this approach provides a model in which the cellular interactions involved in both positive and negative selection can be studied under controlled in vitro conditions.
我们描述了一种体外系统,在该系统中,发育中的T细胞在特定的基质细胞制剂上进行阳性选择,这些制剂包括主要组织相容性复合体II类阳性上皮细胞,但不包括骨髓来源的细胞。在这个系统中,双阳性T细胞受体阴性(TCR-)、CD4+8+胸腺细胞成熟为单阳性TCR+、CD4+和CD8+细胞的过程与功能能力的发展同时发生。与体内情况一样,随着细胞从双阳性状态转变为单阳性状态,这种成熟与TCR水平的上调相关。我们还表明,这些培养物中的II类阳性上皮细胞在通过超抗原葡萄球菌肠毒素B介导Vβ8+细胞的缺失(阴性选择)方面比树突状细胞效率更低。这种方法首次提供了一个模型,在该模型中,可以在可控的体外条件下研究参与阳性和阴性选择的细胞相互作用。