p21WAF1/Cip1 suppresses keratinocyte differentiation independently of the cell cycle through transcriptional up-regulation of the IGF-I gene

被引:28
作者
Devgan, Vikram
Nguyen, Bach-Cuc
Oh, Heysun
Dotto, G. Paolo
机构
[1] Univ Lausanne, Dept Biochem, CH-1066 Epalinges, Switzerland
[2] Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Charlestown, MA 02129 USA
[3] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
关键词
D O I
10.1074/jbc.M604684200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:30463 / 30470
页数:8
相关论文
共 43 条
[1]  
Adamo ML., 1995, DIABETES REV, V3, P2
[2]   EphA receptors direct the differentiation of mammalian neural precursor cells through a mitogen-activated protein kinase-dependent pathway [J].
Aoki, M ;
Yamashita, T ;
Tohyama, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (31) :32643-32650
[3]   Apoptosis inhibitory activity of cytoplasmic p21Cip1/WAF1 in monocytic differentiation [J].
Asada, M ;
Yamada, T ;
Ichijo, H ;
Delia, D ;
Miyazono, K ;
Fukumuro, K ;
Mizutani, S .
EMBO JOURNAL, 1999, 18 (05) :1223-1234
[4]   p21WAF1/CIP1 acts as a brake in osteoblast differentiation [J].
Bellosta, P ;
Masramon, L ;
Mansukhani, A ;
Basilico, C .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (05) :818-826
[5]   A function of p21 during promyelocytic leukemia cell differentiation independent of CDK inhibition and cell cycle arrest [J].
Casini, T ;
Pelicci, PG .
ONCOGENE, 1999, 18 (21) :3235-3243
[6]   BMP-2 and insulin-like growth factor-I mediate osterix (Osx) expression in human mesenchymal stem cells via the MAPK and protein kinase D signaling pathways [J].
Celil, AB ;
Campbell, PG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (36) :31353-31359
[7]   Effects of p21Waf1/Cip1/Sdi1 on cellular gene expression:: Implications for carcinogenesis, senescence, and age-related diseases [J].
Chang, BD ;
Watanabe, K ;
Broude, EV ;
Fang, J ;
Poole, JC ;
Kalinichenko, TV ;
Roninson, IB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :4291-4296
[8]   Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40
[9]   Functional interaction of STAT3 transcription factor with the cell cycle inhibitor p21WAF1/CIP1/SD11 [J].
Coqueret, O ;
Gascan, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (25) :18794-18800
[10]   P21WAF1/Cip1 is a negative transcriptional regulator of Wnt4 expression downstream of Notch1 activation [J].
Devgan, V ;
Mammucari, C ;
Millar, SE ;
Brisken, C ;
Dotto, GP .
GENES & DEVELOPMENT, 2005, 19 (12) :1485-1495