The in vitro and in vivo skin-whitening activity of Ectoine through enhanced autophagy in melanocytes and keratinocytes and zebrafish model

IF 5 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
BioFactors Pub Date : 2025-02-05 DOI:10.1002/biof.70004
Wei-Chen Jane, Siang-Jyun Chen, Jhih-Hsuan Hseu, Xuan-Zao Chen, Sudhir Pandey, Hsueh-Wei Chang, Hsin-Ling Yang, You-Cheng Hseu, Yung-Luen Yu
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引用次数: 0

Abstract

Ectoine, a natural bacterial osmolyte, suppressed UVA irradiated-α-melanocyte stimulating hormone (MSH) stimulated melanogenesis through antioxidant Nrf2 pathways in human keratinocytes; however, the underlying skin whitening mechanisms were not elucidated. The depigmenting efficiency of Ectoine (0–400 μM) through antimelanogenesis and melanin degradation by autophagy promotion was investigated in melanoma (B16F10) and melanin-feeding keratinocyte (HaCaT) cells and in vivo zebrafish model. MTT assay, Western blotting, GFP-LC3 puncta, AVO formation, melanin assay, immunofluorescence staining, TEM techniques, siLC3 transfection, and zebrafish model were utilized. Ectoine-induced autophagy in B16F10 and HaCaT cells was shown by enhanced LC3-II accumulation, autophagosome GFP-LC3 puncta, autolysosome AVOs formation, ATG4B downregulation, and Beclin-1/Bcl-2 dysregulation. The immunoprecipitation data revealed that Ectoine increased the association between LC3-II and p62 proteins in B16F10 and HaCaT cells. Importantly, antioxidant NAC pretreatment antagonized the Ectoine-induced ATG4B diminution in B16F10 and HaCaT cells. Ectoine inhibited melanogenesis by suppressing melanosome gp100, tyrosinase, TRP-1/-2, and/or melanin formation via autophagy in α-MSH-stimulated B16F10 and melanin-feeding HaCaT cells. TEM findings displayed that Ectoine increased melanosome-engulfing autophagosomes and autolysosomes in α-MSH-stimulated B16F10 and melanin-feeding HaCaT cells. Ectoine-inhibited melanogenesis in α-MSH-stimulated B16F10 cells and melanin-feeding HaCaT cells was reversed by pretreatment with the autophagy inhibitor 3-MA or LC3 silencing. In vivo study demonstrated that Ectoine (5 mM) suppressed endogenous body pigmentation by antimelanogenesis and melanin degradation through autophagy induction in a zebrafish model. The in vitro and in vivo study demonstrated that Ectoine inhibits melanogenesis and enhances melanin degradation by triggering autophagy. Ectoine could be utilized as a whitening ingredient in cosmetic formulations.

Abstract Image

通过增强黑素细胞和角质形成细胞的自噬以及斑马鱼模型,研究Ectoine体外和体内皮肤美白活性
异托因是一种天然的细菌渗透剂,抑制UVA照射下的-α-促黑素细胞激素(MSH)通过抗氧化Nrf2途径刺激人角质形成细胞的黑色素生成;然而,潜在的皮肤美白机制尚未阐明。在黑素瘤(B16F10)细胞、供黑色素的角化细胞(HaCaT)细胞和斑马鱼体内模型中,研究了Ectoine (0-400 μM)通过抗黑色素生成和促进自噬降解黑色素的脱色效率。采用MTT法、Western blotting法、GFP-LC3斑点法、AVO形成法、黑色素法、免疫荧光染色法、TEM技术、siLC3转染法、斑马鱼模型。外泌素诱导的B16F10和HaCaT细胞自噬表现为LC3-II积累增强、自噬小体GFP-LC3点、自噬小体AVOs形成、ATG4B下调、Beclin-1/Bcl-2失调。免疫沉淀数据显示,Ectoine增加了B16F10和HaCaT细胞中LC3-II和p62蛋白之间的关联。重要的是,抗氧化剂NAC预处理可拮抗ectoine诱导的B16F10和HaCaT细胞中ATG4B的减少。外托因通过抑制α- msh刺激的B16F10细胞和黑色素喂养的HaCaT细胞中的黑色素小体gp100、酪氨酸酶、TRP-1/-2和/或自噬生成黑色素来抑制黑色素的形成。透射电镜结果显示,在α- msh刺激的B16F10细胞和黑色素喂养的HaCaT细胞中,外托碱增加了吞噬黑色素体的自噬体和自溶体。经自噬抑制剂3-MA或LC3沉默预处理后,α- msh刺激的B16F10细胞和黑色素供血的HaCaT细胞的黑色素生成被ectoine抑制。体内研究表明,在斑马鱼模型中,Ectoine (5 mM)通过抗黑色素生成和自噬诱导的黑色素降解抑制内源性色素沉着。体外和体内研究表明,Ectoine通过触发自噬来抑制黑色素生成并促进黑色素降解。依托因可以用作化妆品配方中的美白成分。
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来源期刊
BioFactors
BioFactors 生物-内分泌学与代谢
CiteScore
11.50
自引率
3.30%
发文量
96
审稿时长
6-12 weeks
期刊介绍: BioFactors, a journal of the International Union of Biochemistry and Molecular Biology, is devoted to the rapid publication of highly significant original research articles and reviews in experimental biology in health and disease. The word “biofactors” refers to the many compounds that regulate biological functions. Biological factors comprise many molecules produced or modified by living organisms, and present in many essential systems like the blood, the nervous or immunological systems. A non-exhaustive list of biological factors includes neurotransmitters, cytokines, chemokines, hormones, coagulation factors, transcription factors, signaling molecules, receptor ligands and many more. In the group of biofactors we can accommodate several classical molecules not synthetized in the body such as vitamins, micronutrients or essential trace elements. In keeping with this unified view of biochemistry, BioFactors publishes research dealing with the identification of new substances and the elucidation of their functions at the biophysical, biochemical, cellular and human level as well as studies revealing novel functions of already known biofactors. The journal encourages the submission of studies that use biochemistry, biophysics, cell and molecular biology and/or cell signaling approaches.
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