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


Autoria(s): Wang J.; Devgan V.; Corrado M.; Prabhu N.S.; El-Deiry W.S.; Riccardi C.; Pandolfi P.P.; Missero C.; Dotto G.P.
Data(s)

2005

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_E1EE33F41E68

isbn:0021-9258 (Print)

pmid:16155000

doi:10.1074/jbc.M507976200

isiid:000233044500050

Idioma(s)

en

Fonte

Journal of Biological Chemistry, vol. 280, no. 45, pp. 37725-37731

Palavras-Chave #Animals; Apoptosis/radiation effects; Cells, Cultured; Cyclin-Dependent Kinase Inhibitor p21/genetics; Cyclin-Dependent Kinase Inhibitor p21/metabolism; Epidermis/cytology; Epidermis/metabolism; Female; Gene Deletion; Glucocorticoids/pharmacology; Keratinocytes/cytology; Keratinocytes/radiation effects; Mice; Receptors, Nerve Growth Factor/metabolism; Receptors, Tumor Necrosis Factor/metabolism; Transcription, Genetic; Ultraviolet Rays
Tipo

info:eu-repo/semantics/article

article