p21WAF1/Cip1 suppresses keratinocyte differentiation independently of the cell cycle through transcriptional up-regulation of the IGF-I gene.
Détails
ID Serval
serval:BIB_2EB8C426A3D0
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
p21WAF1/Cip1 suppresses keratinocyte differentiation independently of the cell cycle through transcriptional up-regulation of the IGF-I gene.
Périodique
Journal of Biological Chemistry
ISSN
0021-9258
Statut éditorial
Publié
Date de publication
10/2006
Peer-reviewed
Oui
Volume
281
Numéro
41
Pages
30463-30470
Langue
anglais
Notes
Publication types: Journal Article
Résumé
p21 plays a dual role in keratinocyte growth and differentiation control. It restricts the number of keratinocyte stem cell populations while inhibiting the later stages of differentiation independently of the cell cycle. The molecular/biochemical mechanism for the differentiation suppressive function of p21 is unknown. Here we show that elevated p21 expression leads to activation of MAPK family members in a keratinocyte-specific and cell cycle-independent manner, and up-regulation of MAPK activity can explain the inhibitory effects of p21 on differentiation. p21 induces transcription of several genes with MAPK activation potential. Although several of these genes are induced by p21 in a MAPK-dependent manner, expression of IGF-I is induced upstream of MAPK activation. IGF-I stimulation is by itself sufficient to cause MAPK activation and inhibit differentiation and suppression of IGF-I signaling by knock down of the cognate receptor (IGF-R1), diminishing the ability of p21 to activate MAPK and suppress differentiation. Thus, in keratinocytes, the ability of p21 to suppress differentiation can be explained by cell type-specific activation of the MAPK cascade by transcriptional up-regulation of the IGF-I gene.
Mots-clé
Animals, Cell Cycle, Cell Differentiation, Cyclin-Dependent Kinase Inhibitor p21/metabolism, Cyclin-Dependent Kinase Inhibitor p21/physiology, Enzyme Activation, Epidermis/metabolism, Gene Expression Regulation, Insulin-Like Growth Factor I/biosynthesis, Insulin-Like Growth Factor I/genetics, Keratinocytes/cytology, Keratinocytes/metabolism, MAP Kinase Signaling System, Mice, Promoter Regions, Genetic, Transcription, Genetic
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/01/2008 14:58
Dernière modification de la notice
20/08/2019 13:13