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真黑素的生物合成受酪氨酸酶和酪氨酸酶相关蛋白-1基因的协同表达调控。

Eumelanin biosynthesis is regulated by coordinate expression of tyrosinase and tyrosinase-related protein-1 genes.

作者信息

Kuzumaki T, Matsuda A, Wakamatsu K, Ito S, Ishikawa K

机构信息

Department of Biochemistry, Yamagata University School of Medicine, Japan.

出版信息

Exp Cell Res. 1993 Jul;207(1):33-40. doi: 10.1006/excr.1993.1159.

Abstract

Melanin is specifically produced in melanocytes. The pathway for melanin biosynthesis is regulated by a number of melanocyte-specific proteins, including tyrosinase and tyrosinase-related protein-1 (TRP-1, b locus protein). To understand the regulation of melanogenesis, we examined tyrosinase activities, mRNA levels of tyrosinase and TRP-1, and eumelanin and pheomelanin contents in mouse B16-F1 melanoma cells after they had been treated with some melanotropic reagents. Cholera toxin, alpha-melanocyte-stimulating hormone, and dibutyryl cyclic AMP increased tyrosinase activity and stimulated eumelanin biosynthesis. These reagents elevated intracellular cAMP levels. In contrast, 12-O-tetradecanoylphorbol 13-acetate reduced tyrosinase activity and eumelanin synthesis. In all cases, the mRNA levels of tyrosinase and TRP-1 changed in parallel with tyrosinase activity and eumelanin content. TRP-1 was induced simultaneously with tyrosinase, although its inducibility was lower than that of tyrosinase. These results suggest that the expressions of tyrosinase and TRP-1 genes are coordinately regulated by melanotropic reagents through cAMP-dependent protein kinase and protein kinase C in mouse B16-F1 cells, and that their coordinate expression causes eumelanin biosynthesis.

摘要

黑色素专门在黑素细胞中产生。黑色素生物合成途径受多种黑素细胞特异性蛋白调控,包括酪氨酸酶和酪氨酸酶相关蛋白-1(TRP-1,b位点蛋白)。为了解黑色素生成的调控机制,我们检测了用某些促黑素试剂处理后的小鼠B16-F1黑色素瘤细胞中的酪氨酸酶活性、酪氨酸酶和TRP-1的mRNA水平以及真黑素和褐黑素含量。霍乱毒素、α-黑素细胞刺激素和二丁酰环磷酸腺苷增加了酪氨酸酶活性并刺激了真黑素生物合成。这些试剂提高了细胞内cAMP水平。相反,12-O-十四酰佛波醇-13-乙酸酯降低了酪氨酸酶活性和真黑素合成。在所有情况下,酪氨酸酶和TRP-1的mRNA水平与酪氨酸酶活性和真黑素含量平行变化。TRP-1与酪氨酸酶同时被诱导,尽管其诱导性低于酪氨酸酶。这些结果表明,在小鼠B16-F1细胞中,促黑素试剂通过cAMP依赖性蛋白激酶和蛋白激酶C协同调节酪氨酸酶和TRP-1基因的表达,并且它们的协同表达导致真黑素生物合成。

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