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3,6-脱水-l-半乳糖对人黑素细胞和皮肤等效模型中α-促黑素细胞激素诱导的黑素生成的影响。

Effect of 3,6-anhydro-l-galactose on α-melanocyte stimulating hormone-induced melanogenesis in human melanocytes and a skin-equivalent model.

机构信息

Department of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Republic of Korea.

Korean Medicine Application Center, Korea Institute of Oriental Medicine, Daegu, Republic of Korea.

出版信息

J Cell Biochem. 2018 Sep;119(9):7643-7656. doi: 10.1002/jcb.27112. Epub 2018 Jun 5.

DOI:10.1002/jcb.27112
PMID:29870090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6175185/
Abstract

3,6-Anhydro-l-galactose (l-AHG) is a bioactive sugar that is a major component of agarose. Recently, l-AHG was reported to have anti-melanogenic potential in human epidermal melanocytes (HEMs) and B16F10 melanoma cells; however, its underlying molecular mechanisms remain unknown. At noncytotoxic concentrations, l-AHG has been shown to inhibit alpha-melanocyte-stimulating hormone-induced melanin synthesis in various cell models, including HEMs, melan-a cells, and B16F10 cells. Although l-AHG did not inhibit tyrosinase activity in vitro, reverse transcription-polymerase chain reaction results demonstrated that the anti-melanogenic effect of l-AHG was mediated by transcriptional repression of melanogenesis-related genes, including tyrosinase, tyrosinase-related protein-1 (TRP-1), tyrosinase-related protein-2 (TRP-2), and microphthalmia-associated transcription factor (MITF) in HEMs. Western blot analysis showed that l-AHG effectively attenuated α-melanocyte-stimulating hormone-induced melanogenic proteins by inhibiting cyclic adenosine monophosphate/cyclic adenosine monophosphate-dependent protein kinase, mitogen-activated protein kinase, and Akt signaling pathways in HEMs. Topical application of l-AHG significantly ameliorated melanin production in a 3D pigmented human skin model. Collectively, these results suggest that l-AHG could be utilized as novel cosmetic compounds with skin-whitening efficacy.

摘要

3,6-脱水-l-半乳糖(l-AHG)是一种具有生物活性的糖,是琼脂糖的主要成分。最近,据报道 l-AHG 对人表皮黑素细胞(HEMs)和 B16F10 黑色素瘤细胞具有抗黑色素生成作用;然而,其潜在的分子机制尚不清楚。在非细胞毒性浓度下,l-AHG 已被证明可抑制各种细胞模型(包括 HEMs、melan-a 细胞和 B16F10 细胞)中α-黑色素细胞刺激激素诱导的黑色素合成。尽管 l-AHG 体外不抑制酪氨酸酶活性,但逆转录-聚合酶链反应结果表明,l-AHG 的抗黑色素生成作用是通过转录抑制黑色素生成相关基因介导的,包括 HEMs 中的酪氨酸酶、酪氨酸酶相关蛋白-1(TRP-1)、酪氨酸酶相关蛋白-2(TRP-2)和小眼畸形相关转录因子(MITF)。Western blot 分析表明,l-AHG 通过抑制 HEMs 中的环腺苷酸/环腺苷酸依赖性蛋白激酶、丝裂原激活蛋白激酶和 Akt 信号通路,有效抑制α-黑色素细胞刺激激素诱导的黑色素生成蛋白。l-AHG 的局部应用可显著改善 3D 色素人皮肤模型中的黑色素生成。综上所述,这些结果表明,l-AHG 可用作具有皮肤美白功效的新型化妆品化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/843911e8efe7/JCB-119-7643-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/4357dfbb7c57/JCB-119-7643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/526f72601399/JCB-119-7643-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/b3cfcd7d0ec7/JCB-119-7643-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/b1b57a3a5eaf/JCB-119-7643-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/3fcde5db516c/JCB-119-7643-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/c43a203884e8/JCB-119-7643-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/843911e8efe7/JCB-119-7643-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/4357dfbb7c57/JCB-119-7643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/526f72601399/JCB-119-7643-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/b3cfcd7d0ec7/JCB-119-7643-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/b1b57a3a5eaf/JCB-119-7643-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/3fcde5db516c/JCB-119-7643-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/c43a203884e8/JCB-119-7643-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c019/6175185/843911e8efe7/JCB-119-7643-g007.jpg

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