岩藻聚糖对b16小鼠黑色素瘤细胞黑色素形成及凋亡的影响。

Zhi-Jiang Wang, Wei Xu, Jian-Wen Liang, Cai-Sheng Wang, Yani Kang
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引用次数: 41

摘要

背景:褐藻多糖是从褐藻中提取的一种复合硫酸酸化多糖,具有多种生物活性。它不仅能抑制癌细胞生长,还能在体外抑制酪氨酸酶。因此,研究岩藻聚糖对B16小鼠黑色素瘤细胞的影响是很有意义的,因为这些发现可能为岩藻聚糖抑制黑色素形成的潜在机制提供新的见解。在本研究中,我们旨在研究岩藻聚糖的抗黑素生成作用及其对B16细胞的抑制作用。材料与方法:观察岩藻聚糖对B16黑色素瘤细胞及细胞酪氨酸酶的影响。细胞计数试剂盒-8检测细胞活力。用分光光度法测定细胞酪氨酸酶活性和黑色素含量,免疫印迹法测定细胞蛋白表达。用相差显微镜观察B16黑色素瘤细胞形态学变化,流式细胞术观察细胞凋亡情况。结果:采用细胞活力分析进行体外研究,结果显示岩藻糖聚糖显著降低活细胞数,IC50为550±4.3µg/mL。550µg/mL岩藻糖丹作用48 h后,细胞形态发生改变,细胞明显凋亡。结论:岩藻糖丹抑制B16黑色素瘤细胞增殖和细胞酪氨酸酶活性。岩藻糖聚糖可用于治疗色素沉着和作为皮肤增白剂在化妆品行业。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

EFFECT OF FUCOIDAN ON B16 MURINE MELANOMA CELL MELANIN FORMATION AND APOPTOSIS.

EFFECT OF FUCOIDAN ON B16 MURINE MELANOMA CELL MELANIN FORMATION AND APOPTOSIS.

EFFECT OF FUCOIDAN ON B16 MURINE MELANOMA CELL MELANIN FORMATION AND APOPTOSIS.

EFFECT OF FUCOIDAN ON B16 MURINE MELANOMA CELL MELANIN FORMATION AND APOPTOSIS.

Background: Fucoidan is a complex sulfated polysaccharide extracted from brown seaweed and has a wide variety of biological activities. It not only inhibits cancer cell growth but also inhibits tyrosinase in vitro. Therefore, it is of interest to investigate the effect of fucoidan on B16 murine melanoma cells as the findings may provide new insights into the underlying mechanism regarding the inhibition of melanin formation by fucoidan. In the present study, we aimed to investigate the anti-melanogenic effect of fucoidan and its inhibitory effect on B16 cells.

Materials and methods: The influence of fucoidan on B16 melanoma cells and cellular tyrosinase was examined. Cell viability was examined by the cell counting kit-8 assay. Cellular tyrosinase activity and melanin content were determined using spectrophotometric methods and protein expression was analyzed by immunoblotting. Morphological changes in B16 melanoma cells were examined by phase contrast microscopy and apoptosis was analyzed by flow cytometry.

Results: In vitro studies were performed using cell viability analysis and showed that fucoidan significantly decreased viable cell number in a dose-response manner with an IC50 of 550 ±4.3 µg/mL. Cell morphology was altered and significant apoptosis was induced when cells were exposed to 550 µg/mL fucoidan for 48 h.

Conclusion: This study provides substantial evidence to show that fucoidan inhibits B16 melanoma cell proliferation and cellular tyrosinase activity. Fucoidan may be useful in the treatment of hyperpigmentation and as a skin-whitening agent in the cosmetics industry.

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