Complex regulation of CCR( at multiple discrete stages of T cell development

被引:55
作者
Wurbel, MA
Malissen, B
Campbell, JJ
机构
[1] Childrens Hosp, Joint Program Transfus Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Univ Med Marseille, INSERM, CNRS, Ctr Immunol Marseille Luminy, Marseille, France
关键词
cell trafficking; chemokines; chemotaxis; T cells; thymus;
D O I
10.1002/eji.200535203
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:73 / 81
页数:9
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