Abstract
7,3′,4′-Trihydroxyisoflavone (7,3′,4′-THIF) is a metabolite of daidzein which is a representative isoflavone found in soybean. Recent studies suggested that 7,3′,4′-THIF exerts a hypopigmentary effect in B16F10 cells, however, its underlying molecular mechanisms and specific target protein remain unknown. Here, we found that 7,3′,4′-THIF, but not daidzein, inhibited α-melanocyte-stimulating hormone (MSH)-induced intracellular and extracellular melanin production in B16F10 cells by directly targeting melanocortin 1 receptor (MC1R). Western blot data showed that 7,3′,4′-THIF inhibited α-MSH-induced tyrosinase, tyrosinase-related protein-1 (TYRP-1), and tyrosinase-related protein-2 (TYRP-2) expressions through the inhibition of Microphthalmia-associated transcription factor (MITF) expression and cAMP response element-binding (CREB) phosphorylation. 7,3′,4′-THIF also inhibited α-MSH-induced dephosphorylation of AKT and phosphorylation of p38 and cAMP-dependent protein kinase (PKA). cAMP and Pull-down assays indicated that 7,3′,4′-THIF strongly inhibited forskolin-induced intracellular cAMP production and bound MC1R directly by competing with α-MSH. Moreover, 7,3′,4′-THIF inhibited α-MSH-induced intracellular melanin production in human epidermal melanocytes (HEMs). Collectively, these results demonstrate that 7,3′,4′-THIF targets MC1R, resulting in the suppression of melanin production, suggesting a protective role for 7,3′,4′-THIF against melanogenesis.
Highlights
Melanin, synthesized in human melanocytes, plays an important role in protecting the skin from the harmful effects of ultraviolet (UV) radiation (Solano et al, 2006; Park et al, 2009)
Tyrosinase and tyrosinase-related proteins (TYRPs) expression mainly through cAMP/protein kinase (PKA) signaling and subsequently induces both microphthalmia-associated transcription factor (MITF) expression and cAMP response element-binding protein (CREB) phosphorylation, we investigated whether 7,3,4 THIF inhibited MITF expression and CREB phosphorylation. 7,3,4 -THIF strongly suppressed α-melanocyte-stimulating hormone (α-melanocyte stimulating hormone (MSH))-induced MITF expression and CREB phosphorylation (Figure 2B), suggesting that the whitening effect of 7,3,4 -THIF is mediated by the suppression of melanogenic protein expression in B16F10 cells
The binding ability of 7,3,4 -THIF with melanocortin 1 receptor (MC1R) was altered in a concentration-dependent manner in the presence of α-MSH (Figure 4D), suggesting that 7,3,4 -THIF competes with α-MSH for binding with MC1R. These results suggest that 7,3,4 -THIF is an α-MSH-competitive inhibitor for suppressing MC1R activation
Summary
Melanin, synthesized in human melanocytes, plays an important role in protecting the skin from the harmful effects of ultraviolet (UV) radiation (Solano et al, 2006; Park et al, 2009). Α-MSH stimulates melanocortin 1 receptor (MC1R) and subsequently induces intracellular cAMP production in melanocytes (Solano et al, 2006; Yamaguchi and Hearing, 2009; Gillbro and Olsson, 2011). Elevation of intracellular cAMP stimulates transcriptional factors such as microphthalmia-associated transcription factor (MITF) and cAMP response element-binding protein (CREB) via the cAMPdependent protein kinase (PKA) and p38 MAPK signaling pathways (Busca and Ballotti, 2000; Smalley and Eisen, 2000; Tada et al, 2002; Saha et al, 2006; Solano et al, 2006; Yamaguchi and Hearing, 2009; Gillbro and Olsson, 2011). Suppression of the MC1R signaling pathway may protect strategy against skin hyperpigmentation
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