Petrie H T, Scollay R, Shortman K
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital.
Eur J Immunol. 1992 Aug;22(8):2185-8. doi: 10.1002/eji.1830220836.
Two types of T lymphocytes, distinguishable by their surface expression of either the gamma delta or the alpha beta T cell receptor (TcR) for antigen, populate the periphery in the adult. In addition, immature precursors of both T cell types can be found in the thymus. While it is generally accepted that these two cell types represent distinct lineages, it is not known at which developmental stage these lineages diverge. The most mature thymocyte precursor population not yet expressing T lineage-specific surface markers (i.e. CD3, CD4, and CD8) is known to be capable of generating TcR-alpha beta T cells, and has been thought to be preprogrammed into the TcR-alpha beta lineage at an earlier developmental stage. We now show that this late-stage precursor is capable of giving rise to cells of both the TcR-alpha beta and -gamma delta lineages, both in vitro after intrathymic transplantation, and in vitro in simple culture medium or medium with cytokines. Thus it appears that the divergence of TcR-alpha beta and -gamma delta cells can occur at a relatively late stage of intrathymic development, just prior to the onset of CD4 and CD8 expression in most cells.
在成年个体的外周组织中,存在两种T淋巴细胞,可通过其表面表达的γδ或αβT细胞抗原受体(TcR)加以区分。此外,在胸腺中可发现这两种T细胞类型的未成熟前体细胞。虽然人们普遍认为这两种细胞类型代表不同的谱系,但尚不清楚这些谱系在哪个发育阶段发生分化。已知最成熟的胸腺细胞前体细胞群体尚未表达T谱系特异性表面标志物(即CD3、CD4和CD8),并且能够产生TcR-αβT细胞,人们一直认为该群体在更早的发育阶段就已预先编程进入TcR-αβ谱系。我们现在表明,这种晚期前体细胞能够产生TcR-αβ和-γδ谱系的细胞,无论是在胸腺内移植后的体外实验中,还是在简单培养基或含细胞因子的培养基中的体外实验中。因此,TcR-αβ和-γδ细胞的分化似乎可能发生在胸腺内发育的相对晚期,就在大多数细胞开始表达CD4和CD8之前。