4.5 Article

Glucocorticoid-induced MIF expression by human CEM T cells

Journal

CYTOKINE
Volume 48, Issue 3, Pages 177-185

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.cyto.2009.07.002

Keywords

Glucocorticoid receptor; Inflammation; T cell; Promoter

Funding

  1. NIH
  2. Alliance for Lupus Research
  3. Leenaards Foundation
  4. Studienstiftung des deutschen Volkes
  5. Swiss National Science Foundation
  6. Bristol-Myers Squibb Foundation
  7. Santos-Suarez Foundation for Medical Research

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Macrophage migration inhibitory factor (MIF) is an upstream activator of the immune response that counter-regulates the immunosuppressive effects of glucocorticoids. While MIF is released by cells in response to diverse microbial and invasive stimuli, evidence that glucocorticoids in low concentrations also induce MIF secretion suggests an additional regulatory relationship between these mediators. We investigated the expression of MIF from the human CEM T cell line, which exists in two well-characterized, glucocorticoid-sensitive (CEM-C7) and glucocorticoid-resistant (CEM-C1) variant clones. Dexamethasone in low concentrations induced MIF secretion from CEM-C7 but not CEM-C1 T cells by a bell-shaped dose response that was similar to that reported previously for the release of MIF by monocytes/macrophages. Glucocorticoid stimulation of CEM-C7 T cells was accompanied by an MIF transcriptional response, which by promoter analysis was found to involve the GRE and ATF/CRE transcription factor binding sites. These data support a glucocorticoid-mediated MIF secretion response by T cells that may contribute to the regulation of the adaptive immune response. (C) 2009 Elsevier Ltd. All rights reserved.

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