Rap1, a small GTP-binding protein is upregulated during arrest of proliferation in human keratinocytes

被引:14
作者
D'Silva, NJ
Mitra, RS
Zhang, Z
Kurnit, DM
Babcock, CR
Polverini, PJ
Carey, TE
机构
[1] Univ Michigan, Sch Dent, Dept Oral Med Pathol & Oncol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Ctr Med, Dept Pediat & Human Genet, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Lab Head & Neck Canc Biol, Dept Otolaryngol, Ann Arbor, MI 48109 USA
[4] Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
关键词
D O I
10.1002/jcp.10331
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Rap1 is a small GTP-binding protein (SMG) that exists in two 95% homologous isoforms, rap1A and rap1B. The functions of the rap1 proteins are not well understood. in this report we examined expression and function of rap1 in primary (HOKs) and immortalized (IHOKs) human oral keratinocytes under different growth conditions. In HOKs, rap1 increased with passage number, suggesting a role in differentiation and arrest of proliferation. Similarly, when inhibition of proliferation and differentiation were induced in HOKs by 1.2 mM CaCl2, both rap1 and involucrin increased with increasing concentrations of CaCl2. However, when similar experiments were done with IHOKs, which continue to proliferate in the presence of 1.2 mM CaCl2, the increase in involucrin expression was similar to HOKs but there was no substantial increase in rap1, suggesting that increased expression of rap1 is linked to inhibition of proliferation rather than differentiation of keratinocytes. Upon transfection of immortalized keratinocytes with rapGAP, which inactivates both isoforms of endogenous active rap1, enhanced proliferation was observed. Thus, we conclude that rap1 inhibits proliferation in keratinocytes. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:532 / 540
页数:9
相关论文
共 31 条
[1]   CYCLIC-AMP-DEPENDENT ACTIVATION OF RAP1B [J].
ALTSCHULER, DL ;
PETERSON, SN ;
OSTROWSKI, MC ;
LAPETINA, EG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (18) :10373-10376
[2]   Mitogenic and oncogenic properties of the small G protein rap1b [J].
Altschuler, DL ;
Ribeiro-Neto, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (13) :7475-7479
[3]   RAS GENES [J].
BARBACID, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :779-827
[4]   BIOLOGY OF THE RAP PROTEINS, MEMBERS OF THE RAS SUPERFAMILY OF GTP-BINDING PROTEINS [J].
BOKOCH, GM .
BIOCHEMICAL JOURNAL, 1993, 289 :17-24
[5]   THE ABSENCE OF HARVEY RAS MUTATIONS DURING DEVELOPMENT AND PROGRESSION OF SQUAMOUS-CELL CARCINOMAS OF THE HEAD AND NECK [J].
CLARK, LJ ;
EDINGTON, K ;
SWAN, IRC ;
MCLAY, KA ;
NEWLANDS, WJ ;
WILLS, LC ;
YOUNG, HA ;
JOHNSTON, PW ;
MITCHELL, R ;
ROBERTSON, G ;
SOUTAR, D ;
PARKINSON, EK ;
BIRNIE, GD .
BRITISH JOURNAL OF CANCER, 1993, 68 (03) :617-620
[6]  
Dotto GP, 1999, CRIT REV ORAL BIOL M, V10, P442
[7]   Immunolocalization of Rap1 in the rat parotid gland: Detection on secretory granule membranes [J].
DSilva, NJ ;
DiJulio, DH ;
Belton, CM ;
Jacobson, KL ;
Watson, EL .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1997, 45 (07) :965-973
[8]  
FARRELL F, 1992, J LAB CLIN MED, V120, P533
[9]   Rapid Ca2+-mediated activation of Rap1 in human platelets [J].
Franke, B ;
Akkerman, JWN ;
Bos, JL .
EMBO JOURNAL, 1997, 16 (02) :252-259
[10]   SEVERAL SMALL GTP-BINDING PROTEINS ARE STRONGLY DOWN-REGULATED IN SIMIAN-VIRUS-40 (SV40) TRANSFORMED HUMAN KERATINOCYTES AND MAY BE REQUIRED FOR THE MAINTENANCE OF THE NORMAL PHENOTYPE [J].
GROMOV, PS ;
CELIS, JE .
ELECTROPHORESIS, 1994, 15 (3-4) :474-481