Glucocorticoid-induced tumor necrosis factor receptor (GITR) is a member of the tumor necrosis factor receptor superfamily, is expressed in T lymphocytes, and exerts an anti-apoptotic function in these cells. We reported that GITR is also highly expressed in the skin, specifically in keratinocytes, and that it is under negative transcriptional control of p21(Cip1/WAF1), independently from the cell cycle. Although GITR expression is higher in p21-deficient keratinocytes and skin, it is down-modulated with differentiation and in response to UVB. The combined analysis of keratinocytes with increased GITR expression versus normal keratinocytes and skin of mice with a disruption of the GITR gene indicates that this protein protects keratinocytes from UVB-induced apoptosis both in vitro and in vivo.

Glucocorticoid-induced tumor necrosis factor receptor is a p21Cip1/WAF1 transcriptional target conferring resistance of keratinocytes to UV light-induced apoptosis.

PANDOLFI DE RINALDIS, Pier Paolo;
2005-01-01

Abstract

Glucocorticoid-induced tumor necrosis factor receptor (GITR) is a member of the tumor necrosis factor receptor superfamily, is expressed in T lymphocytes, and exerts an anti-apoptotic function in these cells. We reported that GITR is also highly expressed in the skin, specifically in keratinocytes, and that it is under negative transcriptional control of p21(Cip1/WAF1), independently from the cell cycle. Although GITR expression is higher in p21-deficient keratinocytes and skin, it is down-modulated with differentiation and in response to UVB. The combined analysis of keratinocytes with increased GITR expression versus normal keratinocytes and skin of mice with a disruption of the GITR gene indicates that this protein protects keratinocytes from UVB-induced apoptosis both in vitro and in vivo.
2005
280
37725
37731
http://dx.doi.org/10.1074/jbc.M507976200
Animals; Apoptosis; Cells; Cultured; Cyclin-Dependent Kinase Inhibitor p21; Epidermis; Female; Gene Deletion; Glucocorticoids; Keratinocytes; Mice; Receptors; Nerve Growth Factor; Tumor Necrosis Factor; Transcription; Genetic; Ultraviolet Rays
J. Wang;V. Devgan;M. Corrado;N. S. Prabhu;W. S. El-Deiry;C. Riccardi;P. P. Pandolfi;C. Missero;G. P. Dotto
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/63763
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