Diphlorethohydroxycarmalol inhibits melanogenesis via protein kinase A/cAMP response element‐binding protein and extracellular signal‐regulated kinase‐mediated microphthalmia‐associated transcription factor downregulation in α‐melanocyte stimulating hormone‐stimulated B16F10 melanoma cells and zebrafish

小眼畸形相关转录因子 奶油 酪氨酸酶 蛋白激酶A 黑色素 磷酸化 激酶 生物 MAPK/ERK通路 斑马鱼 细胞生物学 化学 环腺苷酸反应元件结合蛋白 黑色素瘤 分子生物学 黑素细胞 癌症研究 转录因子 生物化学 酶 基因
作者
Yuling Ding,Yunfei Jiang,Seung Tae Im,Seungwon Myung,Hyun Soo Kim,Seung‐Hong Lee
出处
期刊:Cell Biochemistry and Function [Wiley]
卷期号:39 (4): 546-554 被引量:13
标识
DOI:10.1002/cbf.3620
摘要

Abstract Diphlorethohydroxycarmalol (DPHC) is a marine polyphenolic compound derived from brown alga Ishige okamurae . A previously study has suggested that DPHC possesses strong mushroom tyrosinase inhibitory activity. However, the anti‐melanogenesis effect of DPHC has not been reported at cellular level. The objective of the present study was to clarify the melanogenesis inhibitory effect of DPHC and its molecular mechanisms in murine melanoma cells (B16F10) and zebrafish model. DPHC significantly inhibited tyrosinase activity and melanin content dose‐dependently in α‐melanocyte stimulating hormone (α‐MSH)‐stimulated B16F10 cells. This polyphenolic compound also suppressed the expression of phosphorylation of cAMP response element‐binding protein (CREB) by attenuating phosphorylation of cAMP‐dependent protein kinase A, resulting in decreased MITF expression levels. Furthermore, DPHC downregulated MITF protein expression levels by promoting the phosphorylation of extracellular signal‐regulated kinase. It also inhibited tyrosinase, tyrosinase‐related protein 1 (TRP‐1), and TRP‐2 in α‐MSH stimulated B16F10 cells. In in vivo studies using zebrafish, DPHC also markedly inhibited melanin synthesis in a dose‐dependent manner. These results demonstrate that DPHC can effectively inhibit melanogenesis in melanoma cells in vitro and in zebrafish in vivo, suggesting that DPHC could be applied in fields of pharmaceutical and cosmeceuticals as a skin‐whitening agent. Significance of study : The present study showed for the first time that DPHC could inhibit a‐MSH‐stimulated melanogenesis via PKA/CREB and ERK pathway in melanoma cells. It also could inhibit pigmentation in vivo in a zebrafish model. This evidence suggests that DPHC has potential as a skin whitening agent. Taken together, DPHC could be considered as a novel anti‐melanogenic agent to be applied in cosmetic, food, and medical industry.
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