TSC-22D proteins: new regulators of cell homeostasis?

The GILZ (glucocorticoid-induced leucine zipper) protein has first been identified as a glucocorticoid-responsive gene and is now presented as a major regulator of inflammation. Expanding literature documents a role for GILZ as a mediator of the immuno-modulatory and anti-inflammatory effects of glu...

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Veröffentlicht in:M.S. Médecine sciences 2015-01, Vol.31 (1), p.75-83
Hauptverfasser: Pépin, Aurélie, Biola-Vidamment, Armelle, Latré de Laté, Perle, Espinasse, Marie-Alix, Godot, Véronique, Pallardy, Marc
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Sprache:fre
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Zusammenfassung:The GILZ (glucocorticoid-induced leucine zipper) protein has first been identified as a glucocorticoid-responsive gene and is now presented as a major regulator of inflammation. Expanding literature documents a role for GILZ as a mediator of the immuno-modulatory and anti-inflammatory effects of glucocorticoids, mainly through interference with key signal transduction pathways such as nuclear factor-kappa B (NF-kB) or activated protein-1 (AP-1). The TSC-22 (TGF-β-stimulated clone-22) protein is described as an apoptosis modulator and as a new tumor suppressor gene. GILZ and TSC-22, characterized by the presence of a leucine zipper domain and a TSC-box, belong to the TSC-22D (TSC-22 domain) family of proteins which comprises today 18 members. Functions of these proteins suggest that this family plays a major role in cell homeostasis and in the regulation of the immune system.
ISSN:0767-0974
DOI:10.1051/medsci/20153101016