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PMID: 12393603 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Synthesis of glucocorticoid-induced leucine zipper (GILZ) by macrophages: an anti-inflammatory and immunosuppressive mechanism shared by glucocorticoids and IL-10.

Blood ·Vol. 101 ·No. 2 ·2003-01-15 ·Pages 729-38

Berrebi D, Bruscoli S, Cohen N, Foussat A, Migliorati G, Bouchet-Delbos L, Maillot MC, Portier A, Couderc J, Galanaud P, Peuchmaur M, Riccardi C, Emilie D

Abstract

Glucocorticoids and interleukin 10 (IL-10) prevent macrophage activation. In murine lymphocytes, glucocorticoids induce expression of glucocorticoid-induced leucine zipper (GILZ), which prevents the nuclear factor kappaB (NF-kappaB)-mediated activation of transcription. We investigated whether GILZ could account for the deactivation of macrophages by glucocorticoids and IL-10. We found that GILZ was constitutively produced by macrophages in nonlymphoid tissues of humans and mice. Glucocorticoids and IL-10 stimulated the production of GILZ by macrophages both in vitro and in vivo. Transfection of the macrophagelike cell line THP-1 with the GILZ gene inhibited the expression of CD80 and CD86 and the production of the proinflammatory chemokines regulated on activation normal T-cell expressed and secreted (CCL5) and macrophage inflammatory protein 1alpha (CCL3). It also prevented toll-like receptor 2 production induced by lipopolysaccharide, interferongamma, or an anti-CD40 mAb, as well as NF-kappaB function. In THP-1 cells treated with glucocorticoids or IL-10, GILZ was associated with the p65 subunit of NF-kappaB. Activated macrophages in the granulomas of patients with Crohn disease or tuberculosis do not produce GILZ. In contrast, GILZ production persists in tumor-infiltrating macrophages in Burkitt lymphomas. Therefore, GILZ appears to play a key role in the anti-inflammatory and immunosuppressive effects of glucocorticoids and IL-10. Glucocorticoid treatment stimulates GILZ production, reproducing an effect of IL-10, a natural anti-inflammatory agent. The development of delayed-type hypersensitivity reactions is associated with the down-regulation of GILZ gene expression within lesions. In contrast, the persistence of GILZ gene expression in macrophages infiltrating Burkitt lymphomas may contribute to the failure of the immune system to reject the tumor.

MeSH Terms
Animals Antigens, CD/biosynthesis,drug effects B7-1 Antigen/biosynthesis,drug effects B7-2 Antigen Chemokines/biosynthesis Drosophila Proteins Gene Expression Regulation/drug effects Glucocorticoids/pharmacology Humans Immune Tolerance Inflammation/immunology Interleukin-10/pharmacology Leucine Zippers/immunology Macrophages/drug effects,metabolism Membrane Glycoproteins/biosynthesis,drug effects Mice Mice, Transgenic Monocytes/drug effects,metabolism NF-kappa B/metabolism Organ Specificity Receptors, Cell Surface/biosynthesis,drug effects Toll-Like Receptor 2 Toll-Like Receptors Transcription Factors/biosynthesis,drug effects,pharmacology
Chemicals
Antigens, CD B7-1 Antigen B7-2 Antigen CD86 protein, human Cd86 protein, mouse Chemokines Drosophila Proteins Dsip1 protein, mouse Glucocorticoids Membrane Glycoproteins NF-kappa B Receptors, Cell Surface TLR2 protein, human TSC22D3 protein, human Toll-Like Receptor 2 Toll-Like Receptors Transcription Factors Interleukin-10
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Berrebi Dominique
Institut National de la Santé et de la Recherche Médicale (INSERM) U131, Institut Paris-Sud sur les Cytokines, Clamart, France.
Bruscoli Stefano
Cohen Nicolas
Foussat Arnaud
Migliorati Graziella
Bouchet-Delbos Laurence
Maillot Marie-Christine
Portier Alain
Couderc Jacques
Galanaud Pierre
Peuchmaur Michel
Riccardi Carlo
Emilie Dominique
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2003-01-15
Epub
2002-00-12
Pages
729-38
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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