Downregulation of tyrosinase activity in human melanocyte cell cultures by yohimbine

被引:32
作者
Fuller, BB [1 ]
Drake, MA [1 ]
Spaulding, DT [1 ]
Chaudhry, F [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73104 USA
关键词
adrenergic receptors; cAMP; forskolin; melanosomes;
D O I
10.1046/j.1523-1747.2000.00860.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Treatment of human melanocyte cell cultures with the alpha-2 adrenergic receptor antagonist yohimbine results in a marked down-regulation of tyrosinase activity. A 30% decrease occurs within 12 h of exposure of cells to yohimbine (100 mu M), and by 48 h tyrosinase activity in treated melanocytes is less than a fifth that of control cultures, The inhibition is dose dependent and occurs in human melanocytes derived from either black or white skin types, and also in mouse melanoma cells. The yohimbine-induced decrease in tyrosinase activity is reversible, with enzyme levels returning to 90% of control values 48 h after removal of drug. Although tyrosinase activity is markedly suppressed by yohimbine, the compound has no effect on cell proliferation, cellular translation, or DNA synthesis. Treatment of melanocyte cultures with yohimbine blocks the increase in tyrosinase activity by either 3-isobutyl-1-methylxanthine, dibutyryl cAMP, or forskolin, Results of cAMP immunoassays, show that intracellular levels of the cyclic nucleotide are unaffected in cells treated with yohimbine, Tyrosinase inhibition by yohimbine does not involve a decrease in substrate availability since tyrosine uptake studies show that yohimbine has no effect on the amount of tyrosine entering the cell. Incubation of a melanosome-enriched fraction with yohimbine does not clause a lowering of tyrosinase activity, suggesting that an intact cell is required for yohimbine action. In addition, tyrosinase extracts show no reduction in activity when incubated directly with yohimbine, indicating that the drug does not act as a direct inhibitor of the enzyme, Finally, results of western immunoblotting show that yohimbine does not significantly lower the amount of tyrosinase protein in human melanocytes. These findings suggest that yohimbine acts through an as yet unidentified signaling pathway to lower the catalytic activity of pre-existing tyrosinase molecules present in melanocytes.
引用
收藏
页码:268 / 276
页数:9
相关论文
共 41 条
[1]   MITOGENIC AND MELANOGENIC STIMULATION OF NORMAL HUMAN MELANOCYTES BY MELANOTROPIC PEPTIDES [J].
ABDELMALEK, Z ;
SWOPE, VB ;
SUZUKI, I ;
AKCALI, C ;
HARRIGER, MD ;
BOYCE, ST ;
URABE, K ;
HEARING, VJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (05) :1789-1793
[2]  
ABDELMALEK ZA, 1987, CANCER RES, V47, P3141
[3]   In B16 melanoma cells, the inhibition of melanogenesis by TPA results from PKC activation and diminution of microphthalmia binding to the M-box of the tyrosinase promoter [J].
Bertolotto, C ;
Bille, K ;
Ortonne, JP ;
Ballotti, R .
ONCOGENE, 1998, 16 (13) :1665-1670
[4]   Regulation of tyrosinase gene expression by cAMP in B16 melanoma cells involves two CATGTG motifs surrounding the TATA box: Implication of the microphthalmia gene product [J].
Bertolotto, C ;
Bille, K ;
Ortonne, JP ;
Ballotti, R .
JOURNAL OF CELL BIOLOGY, 1996, 134 (03) :747-755
[5]   Effect of arbutin on melanogenic proteins in human melanocytes [J].
Chakraborty, AK ;
Funasaka, Y ;
Komoto, M ;
Ichihashi, M .
PIGMENT CELL RESEARCH, 1998, 11 (04) :206-212
[6]   PHOTOAFFINITY-LABELING OF MSH RECEPTORS ON ANOLIS MELANOPHORES - EFFECTS OF CATECHOLAMINES, CALCIUM AND FORSKOLIN [J].
EBERLE, AN ;
GIRARD, J .
JOURNAL OF RECEPTOR RESEARCH, 1985, 5 (01) :59-81
[7]   Inhibition of the mitogen-activated protein kinase pathway triggers B16 melanoma cell differentiation [J].
Englaro, W ;
Bertolotto, C ;
Buscà, R ;
Brunet, A ;
Pagès, G ;
Ortonne, JP ;
Ballotti, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9966-9970
[8]   HORMONAL-REGULATION OF MELANOGENESIS IN MOUSE MELANOMA AND IN HUMAN MELANOCYTES [J].
FULLER, BB ;
RUNGTA, D ;
IOZUMI, K ;
HOGANSON, GE ;
CORN, TD ;
CAO, VA ;
RAMADAN, ST ;
OWENS, KC .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1993, 680 :302-319
[9]   DOWN-REGULATION OF TYROSINASE MESSENGER-RNA LEVELS IN MELANOMA-CELLS BY TUMOR PROMOTERS AND BY INSULIN [J].
FULLER, BB ;
NIEKRASZ, I ;
HOGANSON, GE .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1990, 72 (02) :81-87
[10]  
FULLER BB, 1987, J BIOL CHEM, V262, P4024