Wurbel Marc-André, Malissen Bernard, Campbell James J
Joint Program in Transfusion Medicine, Children's Hospital, Boston, MA 02115, USA.
Eur J Immunol. 2006 Jan;36(1):73-81. doi: 10.1002/eji.200535203.
We have conducted a comprehensive assessment of CCR9 expression and function at the important milestone stages of murine thymocyte development. We reveal an unusually complex regulatory pattern, in which CCR9 influences T cell development at several widely dispersed stages. We find that CCR9 is not expressed within the thymus until the double-negative (DN)3 stage, although it appears to contribute to T cell precursor development prior to residence in the thymus. CCR9 expression is influenced by pre-T cell receptor signals, and is dramatically up-regulated in a population that appears to be transitional between the DN4 and double-positive stages. In the periphery, functional CCR9 is expressed by all naive CD8 T cells, but not by naive CD4 T cells. To our knowledge, this latter finding is the first difference observed in homing receptor expression between naive lymphocyte populations. This suggests that naive CD8 T cells might have access to lymphoid microenvironments from which naive CD4 T cells are excluded.
我们在小鼠胸腺细胞发育的重要关键阶段对CCR9的表达和功能进行了全面评估。我们揭示了一种异常复杂的调控模式,其中CCR9在几个广泛分散的阶段影响T细胞发育。我们发现,CCR9直到双阴性(DN)3阶段才在胸腺内表达,尽管它似乎在驻留在胸腺之前就对T细胞前体发育有贡献。CCR9的表达受前T细胞受体信号影响,并在一个似乎处于DN4和双阳性阶段之间过渡的群体中显著上调。在外周,所有初始CD8 T细胞均表达功能性CCR9,但初始CD4 T细胞不表达。据我们所知,后一发现是在初始淋巴细胞群体之间归巢受体表达中观察到的首个差异。这表明初始CD8 T细胞可能能够进入初始CD4 T细胞被排除在外的淋巴微环境。