Transcription of melanogenesis enzymes in melanocytes: Dependence upon culture conditions and co-cultivation with keratinocytes

被引:22
作者
Kippenberger, S
Bernd, A
BereiterHahn, J
RamirezBosca, A
Kaufmann, R
Holzmann, H
机构
[1] UNIV FRANKFURT KLINIKUM,ZNETRUM DERMATOL & VENEROL,ABT DERMATOL 1,D-60590 FRANKFURT,GERMANY
[2] UNIV FRANKFURT,INST ZOOL,AK KINEMAT ZELLFORSCH,D-6000 FRANKFURT,GERMANY
来源
PIGMENT CELL RESEARCH | 1996年 / 9卷 / 04期
关键词
melanocytes; co-culture; tyrosinase; TR; TRP; 1; 2;
D O I
10.1111/j.1600-0749.1996.tb00107.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Eumelanogenesis of human skin melanocytes requires at least three enzymes: tyrosinase, TRP 1, and TRP 2. The regulation of these enzymes on transcriptional level was detected in a semiquantitative attempt. The total RNA of melanocytes was reverse-transcripted and followed by a PCR with degenerated primers for all three enzymes. The amplification products were related to each other densitometrically. We examined five different culture conditions: 1) melanocytes in a popular phorbolester containing F-10-medium, 2) melanocytes in a co-culture medium with EGF, 3) melanocytes in a co-culture medium with high calcium, 4) melanocytes co-cultured with keratinocytes in EGF containing co-culture medium, and 5) melanocytes co-cultured with keratinocytes in coculture medium with high calcium. Melanocytes cultured in phorbolester containing F-10-medium featured transcripts of tyrosinase, TRP 1, and TRP 2 in the ratio 45:45:10. The same results were obtained for melanocytes co-cultured with keratinocytes under the two different culture conditions. In melanocytes cultured alone in co-culture media only TRP 1-transcripts were present. It is likely that under co-culture conditions a keratinocyte-derived factor supports the transcription of all three enzymes. For melanocytes in the phorbolester-containing melanocyte medium a proteinkinase C dependent regulation of transcription seems possible.
引用
收藏
页码:179 / 184
页数:6
相关论文
共 42 条
[1]   LEVELS OF DOPACHROME TAUTOMERASE IN HUMAN MELANOCYTES CULTURED IN-VITRO [J].
BERND, A ;
RAMIREZBOSCA, A ;
KIPPENBERGER, S ;
MARTINEZLIARTE, JH ;
HOLZMANN, H ;
SOLANO, F .
MELANOMA RESEARCH, 1994, 4 (05) :287-291
[2]  
Blanchard M M, 1993, PCR Methods Appl, V2, P234
[3]  
Boissy RE, 1996, AM J HUM GENET, V58, P1145
[4]   MOLECULAR CHARACTERIZATION OF A HUMAN TYROSINASE-RELATED-PROTEIN-2 CDNA - PATTERNS OF EXPRESSION IN MELANOCYTIC CELLS [J].
BOUCHARD, B ;
DELMARMOL, V ;
JACKSON, IJ ;
CHERIF, D ;
DUBERTRET, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 219 (1-2) :127-134
[5]   EVIDENCE THAT DOPACHROME TAUTOMERASE IS A FERROUS IRON-BINDING GLYCOPROTEIN [J].
CHAKRABORTY, AK ;
ORLOW, SJ ;
PAWELEK, JM .
FEBS LETTERS, 1992, 302 (02) :126-128
[6]   A SINGLE BASE INSERTION IN THE PUTATIVE TRANSMEMBRANE DOMAIN OF THE TYROSINASE GENE AS A CAUSE FOR TYROSINASE-NEGATIVE OCULOCUTANEOUS ALBINISM [J].
CHINTAMANENI, CD ;
HALABAN, R ;
KOBAYASHI, Y ;
WITKOP, CJ ;
KWON, BS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (12) :5272-5276
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]   NUCLEOTIDE-SEQUENCE OF THE CDNA-ENCODING HUMAN TYROSINASE-RELATED PROTEIN [J].
COHEN, T ;
MULLER, RM ;
TOMITA, Y ;
SHIBAHARA, S .
NUCLEIC ACIDS RESEARCH, 1990, 18 (09) :2807-2808
[9]   GROWTH AND DIFFERENTIATION OF NORMAL HUMAN MELANOCYTES IN A TPA-FREE, CHOLERA TOXIN-FREE, LOW-SERUM MEDIUM AND INFLUENCE OF KERATINOCYTES [J].
DONATIEN, P ;
SURLEVEBAZEILLE, JE ;
THODY, AJ ;
TAIEB, A .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1993, 285 (07) :385-392
[10]   TRANSFORMATION OF MURINE MELANOCYTES BY BASIC FIBROBLAST GROWTH-FACTOR CDNA AND ONCOGENES AND SELECTIVE SUPPRESSION OF THE TRANSFORMED PHENOTYPE IN A RECONSTITUTED CUTANEOUS ENVIRONMENT [J].
DOTTO, GP ;
MOELLMANN, G ;
GHOSH, S ;
EDWARDS, M ;
HALABAN, R .
JOURNAL OF CELL BIOLOGY, 1989, 109 (06) :3115-3128