Influence of retinoic acid on the expression of cytokeratins, vimentin and ICAM-1 in human gingival epithelia in vitro

被引:19
作者
Gao, Z [1 ]
Mackenzie, IC [1 ]
机构
[1] UNIV TEXAS, HLTH SCI CTR, DENT SCI INST, DENT BRANCH 4109, HOUSTON, TX 77225 USA
关键词
gingiva; epithelia; retinoids; cell culture; differentiation;
D O I
10.1111/j.1600-0765.1996.tb00468.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Phenotypic differences exist in vivo between junctional (JE) and oral gingival (OGE) epithelia and an in vitro system has been developed that maintains phenotypic differences. This system, which permits in vitro studies of factors that may influence the epithelial phenotype, was used to investigate the effects of retinoic acid (RA) on epithelial expression of various markers known to distinguish JE from OGE. Primary cultures of JE and OGE were initiated from defined gingival regions and were subcultured and grown for 48 h in 96-well plates or on multiple-well slides. Control cultures were grown in medium supplemented with delipidized serum and all-trans RA was added to experimental groups. Other cultures were grown in a defined RA-free medium. Cultures were examined using monoclonal antibodies against cytokeratins, vimentin, and ICAM-1 and binding displayed by indirect immunocytochemical staining. Staining reactions were assessed by direct microscopic observation and assayed by spectrophotometric quantitation. The results showed that RA had minor effects on the marker expression of JE but markedly enhanced expression of cytokeratins 8, 18, 19, vimentin and ICAM-1 in OGE. These markers, which normally distinguish JE from OGE, were expressed at levels approaching or exceeding those of control JE cultures. These observations indicate that RA responsive mechanisms affect the phenotypes expressed by epithelia in vitro and suggest that such mechanisms may be related to the different phenotypic patterns expressed by gingival epithelia in vivo.
引用
收藏
页码:81 / 89
页数:9
相关论文
共 44 条
[1]  
ASELINEAU D, 1990, DIFFERENTIATION, V45, P221
[2]   HUMAN JUNCTIONAL EPITHELIUM - DEMONSTRATION OF A NEW MARKER, ITS GROWTH-INVITRO AND CHARACTERIZATION BY LECTIN REACTIVITY AND KERATIN EXPRESSION [J].
BAMPTON, JLM ;
SHIRLAW, PJ ;
TOPLEY, S ;
WELLER, P ;
WILTON, JM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 96 (05) :708-717
[3]   REGULATION BY RETINOIC ACID OF ICAM-1 EXPRESSION ON HUMAN TUMOR-CELL LINES [J].
BOUILLON, M ;
TESSIER, P ;
BOULIANNE, R ;
DESTREMPE, R ;
AUDETTE, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1097 (02) :95-102
[4]   ULTRASTRUCTURE OF REGENERATING JUNCTIONAL EPITHELIUM IN THE MONKEY [J].
BRAGA, AM ;
SQUIER, CA .
JOURNAL OF PERIODONTOLOGY, 1980, 51 (07) :386-392
[5]  
CHIOCCA EA, 1988, J BIOL CHEM, V263, P11584
[6]   DISTRIBUTION OF ICAM-1, LFA-3 AND HLA-DR IN HEALTHY AND DISEASED GINGIVAL TISSUES [J].
CRAWFORD, JM .
JOURNAL OF PERIODONTAL RESEARCH, 1992, 27 (04) :291-298
[7]   JUNCTIONAL EPITHELIUM EXPRESSES THE INTERCELLULAR-ADHESION MOLECULE ICAM-1 [J].
CRAWFORD, JM ;
HOPP, B .
JOURNAL OF PERIODONTAL RESEARCH, 1990, 25 (04) :254-256
[8]  
DALE BA, 1991, CRC CRIT REV ORAL BI
[9]  
Darmon M., 1991, SEMINARS DEV BIOL, V2, P219
[10]  
DE LUCA LM, 1991, FASEB J, V5, P2924