首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Protective effects of mannan/beta-glucans from yeast cell wall on the deoxyniyalenol-induced oxidative stress and autophagy in IPEC-J2 cells
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Protective effects of mannan/beta-glucans from yeast cell wall on the deoxyniyalenol-induced oxidative stress and autophagy in IPEC-J2 cells

机译:酵母细胞壁甘露葡聚糖对IPEC-J2细胞脱苏苯酚诱导氧化胁迫和自噬的保护作用

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The aim of this study was to investigate the effects of biomacromolecules mannan/beta-glucans from yeast cell wall (BYCW) to alleviate Deoxynivalenol(DON)-induced injury. Considering that DON has strong oxidizing effect and stimulates autophagy and apoptosis, we examined the effects of BYCW on consequent oxidative stress damage indicators, cells autophagy and apoptosis induced by DON using the porcine jejunum epithelial cell lines (IPEC-J2) as a cell culture model. The results showed that application of BYCW could reverse the decrease of cell viability by DON significantly, and suppress the levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin-8 and -6 (IL-8 and IL-6), except IL-1 beta. Further experiments revealed that BYCW treatment counteracted the DON-induced down-regulation of intracellular glutathione (GSH) and up-regulation of reactive oxygen species (ROS) and malondialdehyde (MDA). Through western blot analysis, we observed that BYCW treatment was able to down-regulate the expression of autophagy protein LC3-II and up-regulate the expression of P62 protein against DON, which suggested that autophagy induced by DON may be suppressed. Altogether, these results indicated a potential ability of supplementation of BYCW to improve cell growth and metabolism as well as the preventive properties of BYCW against the DON-induced cell damage by activating antioxidant system. (C) 2019 Published by Elsevier B.V.
机译:本研究的目的是探讨生物致摩洛甘露甘露葡聚糖从酵母细胞壁(BYCW)的影响,以缓解脱氧肾上腺素(DON)诱导的损伤。考虑到唐具有强烈的氧化效果并刺激自噬和凋亡,我们检查了ByCw对随后的氧化应激损伤指标,通过猪Jejunum上皮细胞系(IPEC-J2)作为细胞培养模型诱导的细胞自噬和凋亡。结果表明,ByCw的应用可以显着逆转细胞活力降低,抑制肿瘤坏死因子-α(TNF-α)和白细胞介素-8和-6(IL-8和IL-6)的水平,除IL-1 Beta外。进一步的实验表明,BYCW治疗抵消了唐诱导的细胞内谷胱甘肽(GSH)的下调和反应性氧物质(ROS)和丙二醛(MDA)的上调。通过Western印迹分析,我们观察到ByCw治疗能够降低自噬蛋白LC3-II的表达,并调节P62蛋白对Don的表达,这表明可以抑制DON诱导的自噬。总共,这些结果表明,通过激活抗氧化系统,通过激活抗氧化系统来补充细胞生长和代谢的潜在能力,提高细胞生长和新陈代谢以及通过扫描抑制唐诱导细胞损伤的预防性。 (c)2019年由elestvier b.v发布。

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