1. ¹Melanogenix Group, Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia
2. ²Queensland Radium Institute Research Unit, Queensland Institute of Medical Research, Brisbane, Queensland, Australia

Correspondence: Dr Richard A. Sturm, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland 4072, Australia. E-mail: R.Sturm@imb.uq.edu.au

Received 11 September 2006; Revised 4 February 2007; Accepted 19 February 2007; Published online 26 April 2007.

Abstract

Upregulation of microphthalmia-associated transcription factor (MITF) expression has been proposed to mediate melanogenesis stimulated by cAMP, whereas downregulation of MITF has been suggested to underlie the depigmentary effects of resveratrol, a promising chemotherapeutic found in red wine. We have assessed the contribution of MITF to pigmentation regulation by treating primary cultures of normal human melanocytes with the adenylate cyclase activator forskolin and/or resveratrol, then quantifying mRNA and protein levels for MITF, tyrosinase, tyrosinase-related protein-1, and dopachrome tautomerase (DCT). The inhibition of tyrosinase activity by resveratrol was not due to alterations in MITF, but instead was explained by both direct tyrosinase inhibition and a post-transcriptional effect that reduced the amount of fully processed tyrosinase. Glycosidase digestion revealed that the basis for the tyrosinase decrease was the retention of an immature form in the ER and subsequent loss of the mature, Golgi-processed enzyme. Elevation of intracellular cAMP by forskolin markedly increased protein levels for MITF, tyrosinase and DCT, however there was no concomitant increase in tyrosinase or DCT mRNA. This indicated that elevated levels of MITF were not sufficient to promote transcription of these melanogenic genes and that the increase in their protein abundance appeared to be predominantly mediated through post-transcriptional processing events.