Jenkinson E J, Kingston R, Owen J J
Nature. 1987;329(6135):160-2. doi: 10.1038/329160a0.
During development, lymphoid stem cells migrate into the thymic rudiment where they proliferate, rearrange their antigen receptor genes and become differentiated into functionally mature T cells. At present, the regulation of these processes is poorly understood, although recent studies have shown that early fetal and adult immature thymocytes express receptors for the T-cell growth factor, interleukin-2 (IL-2). We now present direct evidence that IL-2 receptors have a function in intra-thymic development by demonstrating that proliferation and the generation of cells expressing the T-cell antigen receptor (alpha beta TCR), which is responsible for the recognition of antigens in the context of MHC, are inhibited when antibodies to IL-2 receptors are added to fetal thymus organ cultures. The inhibition is specific in that it does not affect pre-thymic stem cells and can be partially reversed by addition of exogenous recombinant IL-2.
在发育过程中,淋巴样干细胞迁移至胸腺原基,在那里它们增殖、重排抗原受体基因,并分化为功能成熟的T细胞。目前,尽管最近的研究表明早期胎儿和成年未成熟胸腺细胞表达T细胞生长因子白细胞介素-2(IL-2)的受体,但对这些过程的调控仍知之甚少。我们现在提供直接证据表明,IL-2受体在胸腺内发育中具有功能,这是通过证明当将抗IL-2受体抗体添加到胎儿胸腺器官培养物中时,增殖以及表达负责在MHC背景下识别抗原的T细胞抗原受体(αβ TCR)的细胞生成受到抑制来实现的。这种抑制是特异性的,因为它不影响胸腺前体细胞,并且通过添加外源性重组IL-2可部分逆转。