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Positive Effects of Glucocorticoids on T Cell Function by Up-Regulation of IL-7 Receptor α
Author(s) -
Denis Franchimont,
Jérôme Galon,
Melanie S. Vacchio,
Samuel Fan,
Roberta Visconti,
David M. Frucht,
Vincent Geenen,
George P. Chrousos,
Jonathan D. Ashwell,
John J. O’Shea
Publication year - 2002
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.168.5.2212
Subject(s) - glucocorticoid , glucocorticoid receptor , t cell receptor , function (biology) , immune system , receptor , signal transduction , biology , t cell , gene , gene expression , peripheral blood mononuclear cell , microbiology and biotechnology , apoptosis , endocrinology , medicine , immunology , genetics , in vitro
Despite the effects of glucocorticoids on immune function, relatively little is known about glucocorticoid-inducible genes and how their products may regulate lymphocyte function. Using DNA microarray technology to analyze gene expression in PBMC from healthy donors, we identified IL-7Ralpha as a glucocorticoid-inducible gene. This observation was confirmed at the mRNA and protein levels. Conversely, TCR signaling decreased IL-7Ralpha expression, and the relative strength of signaling between these two receptors determined the final IL-7Ralpha levels. The up-regulation of IL-7Ralpha by glucocorticoids was associated with enhanced IL-7-mediated signaling and function. Moreover, IL-7-mediated inhibition of apoptosis at increasing concentrations of glucocorticoids is consistent with enhanced cell sensitivity to IL-7 following glucocorticoid exposure. These observations provide a mechanism by which glucocorticoids may have a positive influence on T cell survival and function.

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