TRANSFORMING GROWTH-FACTOR-BETA UP-REGULATES THE EXPRESSION OF THE GENES FOR BETA-4 INTEGRIN AND BULLOUS PEMPHIGOID ANTIGENS (BPAG1 AND BPAG2) IN NORMAL AND TRANSFORMED HUMAN KERATINOCYTES

被引:19
作者
SOLLBERG, S
RYYNANEN, J
OLSEN, DR
UITTO, J
机构
[1] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT DERMATOL,233 S 10TH ST,ROOM 450,PHILADELPHIA,PA 19107
[2] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT BIOCHEM & MOLEC BIOL,PHILADELPHIA,PA 19107
[3] THOMAS JEFFERSON UNIV,JEFFERSON INST MOLEC MED,MOLEC DERMATOL SECT,PHILADELPHIA,PA 19107
[4] CELTRIX PHARMACEUT INC,DEPT CELL & MOLEC BIOL,SANTA CLARA,CA
关键词
D O I
10.1111/1523-1747.ep12616124
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Three distinct proteins, namely, beta4 integrins, and the 230-kDa (BPAG1) and 180-kDa (BPAG2) bullous pemphigoid antigens, have been shown to co-localize with hemidesmosomes at the dermal-epidermal basement membrane zone. In this study, we examined the expression of the corresponding genes in cultures of normal and transformed human epidermal keratinocytes. The expression of these genes was detected by Northern and in situ hybridizations, and the expression of beta4 integrins was also demonstrated by indirect immunofluorescence. The results indicated clearly detectable expression of all three genes in normal keratinocytes, whereas extremely low or undetectable levels of expression were noted in two transformed cell lines. Addition of TGF-beta1 or TGF-beta2 (10 ng/ml) up-regulated mRNA levels for all three proteins (up to 4.6 times). The increase by TGF-beta1 was particularly striking in keratinocyte cultures incubated in the presence of low (0.15 mM) Ca++, and somewhat less pronounced in the presence of high (1.2 mM) Ca++. The increase in beta4 integrin synthesis was also documented by enhanced immunosignal of the corresponding epitopes. These results indicate that the three hemidesmosomal genes studied here are all responsive to TGF-beta. These observations, together with previous data on the effects of TGF-beta on other components of the skin, suggest that this cytokine may play a role in the development and repair of the cutaneous basement membrane zone.
引用
收藏
页码:409 / 414
页数:6
相关论文
共 45 条
[1]   INTEGRINS AND OTHER CELL-ADHESION MOLECULES [J].
ALBELDA, SM ;
BUCK, CA .
FASEB JOURNAL, 1990, 4 (11) :2868-2880
[2]   DETECTION OF VIRAL SEQUENCES OF LOW REITERATION FREQUENCY BY INSITU HYBRIDIZATION [J].
BRAHIC, M ;
HAASE, AT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (12) :6125-6129
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]   ISOLATION OF A HUMAN EPIDERMAL CDNA CORRESPONDING TO THE 180-KD AUTOANTIGEN RECOGNIZED BY BULLOUS PEMPHIGOID AND HERPES-GESTATIONIS SERA - IMMUNOLOCALIZATION OF THIS PROTEIN TO THE HEMIDESMOSOME [J].
DIAZ, LA ;
RATRIE, H ;
SAUNDERS, WS ;
FUTAMURA, S ;
SQUIQUERA, HL ;
ANHALT, GJ ;
GIUDICE, GJ .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) :1088-1094
[5]   GLUCOCORTICOID-ENHANCED NEOPLASTIC TRANSFORMATION OF HUMAN KERATINOCYTES BY HUMAN PAPILLOMAVIRUS TYPE 16 AND AN ACTIVATED RAS ONCOGENE [J].
DURST, M ;
GALLAHAN, D ;
JAY, G ;
RHIM, JS .
VIROLOGY, 1989, 173 (02) :767-771
[6]   VARIOUS RAT ADULT TISSUES EXPRESS ONLY ONE MAJOR MESSENGER-RNA SPECIES FROM THE GLYCERALDEHYDE-3-PHOSPHATE-DEHYDROGENASE MULTIGENIC FAMILY [J].
FORT, P ;
MARTY, L ;
PIECHACZYK, M ;
ELSABROUTY, S ;
DANI, C ;
JEANTEUR, P ;
BLANCHARD, JM .
NUCLEIC ACIDS RESEARCH, 1985, 13 (05) :1431-1442
[7]   IDENTIFICATION OF 2 COLLAGEN DOMAINS WITHIN THE BULLOUS PEMPHIGOID AUTOANTIGEN, BP180 [J].
GIUDICE, GJ ;
SQUIQUERA, HL ;
ELIAS, PM ;
DIAZ, LA .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (02) :734-738
[8]  
HEINO J, 1989, J BIOL CHEM, V264, P21806
[9]   BASEMENT-MEMBRANE DIVERSITY DETECTED BY MONOCLONAL-ANTIBODIES [J].
HESSLE, H ;
SAKAI, LY ;
HOLLISTER, DW ;
BURGESON, RE ;
ENGVALL, E .
DIFFERENTIATION, 1984, 26 (01) :49-54
[10]   MOLECULAR-CLONING OF THE HUMAN ALPHA-6 INTEGRIN SUBUNIT - ALTERNATIVE SPLICING OF ALPHA-6 MESSENGER-RNA AND CHROMOSOMAL LOCALIZATION OF THE ALPHA-6-GENE AND BETA-4-GENE [J].
HOGERVORST, F ;
KUIKMAN, I ;
VANKESSEL, AG ;
SONNENBERG, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 199 (02) :425-433