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Differential expression of regulator of G‐protein signalling transcripts and in vivo migration of CD4 + naïve and regulatory T cells
Author(s) -
Agenès Fabien,
Bosco Nabil,
Mascarell Laurent,
Fritah Sabrina,
Ceredig Rod
Publication year - 2005
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/j.1365-2567.2005.02146.x
Subject(s) - biology , microbiology and biotechnology , t cell , regulator , regulatory t cell , tcirg1 , immune system , interleukin 21 , il 2 receptor , gene , immunology , genetics
Summary The immune response of T lymphocytes to pathogens is initiated in draining secondary lymphoid organs, and activated cells then migrate to the site of infection. Thus, control of naïve and regulatory CD4 + T‐cell migration is crucial; however, it is poorly understood in physiological and pathological conditions. We found that CD4 + subpopulations displayed characteristic regulator of G‐protein signalling (RGS) gene expression profiles. Regulatory T cells express higher levels of RGS1, RGS9 and RGS16 than naïve cells. These genes are up‐regulated upon cell activation and their level of expression correlates with in vivo cell migration. Using parabiosis, we showed that regulatory T lymphocytes migrate less than naïve T cells and that migrant naïve T cells express even lower RGS levels than their static counterparts. Our results show an inverse correlation between the capacity to migrate and the levels of RGS1, RGS9 and RGS16 for both naïve and regulatory T cells. Taken together, these results suggest a role for RGS molecules in chemokine‐induced lymphocyte migration and demonstrate the peculiarity of regulatory T cells in terms of phenotype and migration ability, providing new insights into their function.