山药多糖对丙烯酰胺诱导RAW264.7细胞极化的影响

Aoni Zhang, Dongliang Jin, Ying Han, Jiankang Wang, Jing Wang
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引用次数: 0

摘要

我们之前发现丙烯酰胺(AA)通过上调P2X7蛋白水平对巨噬细胞RAW264.7细胞造成损伤,山药多糖(YPS)对AA损伤的RAW264.7细胞具有保护作用。巨噬细胞极化可产生与细胞功能密切相关的各种亚型。然而,AA和YPS如何影响RAW264.7极化是未知的。在本研究中,我们研究了AA和YPS对RAW264.7细胞极化的影响。RAW264.7细胞对肿瘤细胞的杀伤作用也得到了评价。结果表明,AA通过升高CD86和COX-2蛋白表达,降低CD206蛋白表达,导致细胞向m1样巨噬细胞极化。抑制P2X7蛋白的表达可有效干扰aa诱导的M1极化。YPS可以通过降低CD86/CD206的比值来调节aa诱导的M1极化,但不影响COX-2蛋白的表达。AA处理RAW264.7细胞培养基对HepG2癌细胞活力无影响,而YPS处理RAW264.7细胞培养基对HepG2细胞活力有明显抑制作用。上述结果提示YPS可调节aa诱导的RAW264.7极化,改善细胞功能。该结果将为进一步解释YPS干预毒性AA的机制提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effects of Yam polysaccharides on acrylamide-induced RAW264.7 cell polarization
We previously found that acrylamide (AA) damaged RAW264.7 cells (a kind of macrophages) by up-regulating P2X7 protein level, and Yam polysaccharides (YPS) could protect RAW264.7 cells against AA injury. Macrophages polarization may generate various subtypes which are closely related with cell function. However, how AA and YPS influence RAW264.7 polarization is unknown. In this study, we studied the effects of AA and YPS on the polarization of RAW264.7 cells. The killing effect of RAW264.7 cell on tumor cells has also been evaluated. The results showed that AA caused cell polarization towards M1-like macrophages by elevating CD86 and COX-2 protein expression and decreasing CD206 protein expression. Inhibiting the expression of P2X7 protein could effectively interfere with AA-induced M1 polarization. YPS could modulate AA-induced M1 polarization by reducing the ratio of CD86/CD206 but not COX-2 protein expression. RAW264.7 cell medium treated with AA had no effect on HepG2 cancer cell viability, but RAW264.7 cell medium treated with YPS significantly inhibited HepG2 cell viability. These findings suggested that YPS could regulate AA-induced RAW264.7 polarization and improve cell function. The results will provide reference for further explaining the mechanism of YPS intervening in toxic AA.
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