miR-144靶向Nrf2,影响氧化鱼油诱导的头巨鲷肠道氧化损伤,重点关注自噬和凋亡

IF 5.1 Q1 ENVIRONMENTAL SCIENCES
Jie Yang , Xiaochuan Zheng , Xin Liu , Qunlan Zhou , Cunxin Sun , Changyou Song , Aimin Wang , Bo Liu
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引用次数: 0

摘要

为了探索miR-144在Nrf2级联反应中的调节作用,并评估其作为减轻氧化鱼油诱导的双头巨鲷肠道损伤靶点的潜力,我们配制了四种实验饲料。以常规饲料为对照饲料(NC),试验饲料分别添加氧化鱼油(of,过氧化值:323 mmol/kg)、of + miR-144阿塔戈米尔和of + miR-144阿塔戈米尔。在氧化鱼油诱导的双氢乙胺(DHE)氧化应激模型中,双氢乙胺(DHE)荧光探针和形态学结果显示,氧化鱼油显著提高了肠细胞内活性氧(ROS)水平,破坏了肠屏障结构,使肠绒毛高度和肌肉层厚度显著降低,肠屏障相关基因ZO-1、Occludin和Claudin-7α显著下调。氧化鱼油处理激活了肠细胞的自噬和凋亡,表现为自噬相关基因Beclin-1、VPS34、P62和ATG5的显著上调(P <;0.05),自噬体增加,凋亡相关基因HSP27、Caspase3、Caspase8、Caspase9显著上调(P <;0.05)。进一步研究表明,miR-144 agomir显著增强Keap1表达,抑制Nrf2表达,而miR-144 antagomir则具有相反的作用。重要的是,通过沉默Nrf2强制表达miR-144诱导ROS积累,提高炎症因子的表达(P <;0.05),甚至进一步诱导自噬和凋亡的发展,而miR-144 antagomir可以通过重新激活Nrf2表达来抵消这种影响。综上所述,本研究表明,沉默miR-144可以通过靶向Nrf2信号通路,保护M. amblycephala肠细胞免受氧化损伤。因此,miR-144有望成为改善氧化油诱导的肠道氧化损伤的调控靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

miR-144 targets Nrf2 affecting the intestinal oxidative damage induced by oxidized fish oil in Megalobrama amblycephala with emphasis on autophagy and apoptosis

miR-144 targets Nrf2 affecting the intestinal oxidative damage induced by oxidized fish oil in Megalobrama amblycephala with emphasis on autophagy and apoptosis
To explore the modulatory role of miR-144 in Nrf2 cascade reactions and assess its potential as a target for alleviating oxidative fish oil-induced intestinal damage in Megalobrama amblycephala, four experimental diets were formulated. A conventional diet was kept as the control diet (NC), while experimental diets consisted of the control diet supplemented with oxidized fish oil (OF, peroxide value: 323 ​mmol/kg), OF ​+ ​miR-144 agomir and OF ​+ ​miR-144 antagomir, respectively. In the oxidative stress model of M. amblycephala induced by oxidized fish oil, dihydroethidium (DHE) fluorescence probe and morphological results revealed that oxidized fish oil markedly elevated the level of reactive oxygen species (ROS) within intestinal cells and destroyed the intestinal barrier structure, such that the height of the intestinal villus and the thickness of the muscle layer were significantly reduced, and intestinal barrier-related genes ZO-1, Occludin and Claudin-7α were significantly down-regulated. Additionally, oxidized fish oil treatment activated autophagy and apoptosis of intestinal cells, which was manifested by the significant up-regulation of autophagy-related genes Beclin-1, VPS34, P62 and ATG5 (P ​< ​0.05), the increase of autophagosomes, and the significant up-regulation of apoptosis-related genes HSP27, Caspase3, Caspase8 and Caspase9 (P ​< ​0.05). Further studies showed that miR-144 agomir significantly enhanced Keap1 expression and inhibited Nrf2 expression, while miR-144 antagomir had the opposite effect. Importantly, forced expression of miR-144 induced ROS accumulation by silencing Nrf2, raised the expression of inflammatory factors (P ​< ​0.05), and even further induced the development of autophagy and apoptosis, while miR-144 antagomir could offset this effect by reactivating Nrf2 expression. In summary, this study showed that silencing miR-144 could protect intestinal cells of M. amblycephala from oxidative damage by targeting the Nrf2 signaling pathway. Therefore, miR-144 is expected to be a regulatory target for ameliorating intestinal oxidative damage induced by oxidized oils.
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