| Literature DB >> 11859107 |
Denis Franchimont1, Jérôme Galon, Melanie S Vacchio, Samuel Fan, Roberta Visconti, David M Frucht, Vincent Geenen, George P Chrousos, Jonathan D Ashwell, John J O'Shea.
Abstract
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.Entities:
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Year: 2002 PMID: 11859107 DOI: 10.4049/jimmunol.168.5.2212
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422