Aroca P, Urabe K, Kobayashi T, Tsukamoto K, Hearing V J
Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1993 Dec 5;268(34):25650-5.
The effect of melanocyte-stimulating hormone (MSH) on the differentiation of mammalian melanocytes has been widely studied since the early 1950s. There have been many reports about the stimulatory effect of MSH on melanin production and specifically on the activity of tyrosinase, the critical enzyme in the melanogenic pathway. However, few and variable results have been obtained concerning the effect of this hormone on the regulation of DOPAchrome tautomerase (TRP2), another melanogenic enzyme which functions later in the melanogenic pathway, or on other melanogenic activities, such as TRP1. In this study, we show that the MSH-induced stimulation of tyrosinase is accompanied by no significant change in the synthesis or catalytic activities of other melanogenic enzymes such as TRP1 or TRP2. This in turn elicits a dramatic increase in melanin production accompanied by a significant decrease in the incorporation of carboxylated precursors into that melanin biopolymer, although the biological implication of that is still unclear.
自20世纪50年代初以来,促黑素细胞激素(MSH)对哺乳动物黑素细胞分化的影响已得到广泛研究。有许多关于MSH对黑色素生成,特别是对酪氨酸酶活性(黑色素生成途径中的关键酶)的刺激作用的报道。然而,关于这种激素对多巴色素互变异构酶(TRP2,黑色素生成途径中稍后起作用的另一种黑色素生成酶)的调节作用,或对其他黑色素生成活性(如TRP1)的影响,所获得的结果很少且各不相同。在本研究中,我们表明,MSH诱导的酪氨酸酶刺激伴随着其他黑色素生成酶(如TRP1或TRP2)的合成或催化活性没有显著变化。这反过来又引发了黑色素生成的显著增加,同时羧化前体掺入该黑色素生物聚合物的量显著减少,尽管其生物学意义仍不清楚。