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Experimental and Computational Studies Investigating Trehalose Protection of HepG2 Cells from Palmitate-Induced Toxicity

机译:实验和计算研究调查海藻糖保护棕榈酸酯诱导的毒性对HepG2细胞的保护。

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摘要

Understanding the mechanism of saturated fatty acid-induced hepatocyte toxicity may provide insight into cures for diseases such as obesity-associated cirrhosis. Trehalose, a nonreducing disaccharide shown to protect proteins and cellular membranes from inactivation or denaturation caused by different stress conditions, also protects hepatocytes from palmitate-induced toxicity. Our results suggest that trehalose serves as a free radical scavenger and alleviates damage from hydrogen peroxide secreted by the compromised cells. We also observe that trehalose protects HepG2 cells by interacting with the plasma membrane to counteract the changes in membrane fluidity induced by palmitate. The experimental results are supported by molecular dynamics simulations of model cell membranes that closely reflect the experimental conditions. Simulations were performed to understand the specific interactions between lipid bilayers, palmitate, and trehalose. The simulations results reveal the early stages of how palmitate induces biophysical changes to the cellular membrane and the role of trehalose in protecting the membrane structure.
机译:了解饱和脂肪酸诱导的肝细胞毒性的机制可能提供对肥胖相关性肝硬化等疾病的治疗方法的见解。海藻糖是一种非还原性的二糖,具有保护蛋白质和细胞膜免受不同应激条件导致的失活或变性的作用,它还可以保护肝细胞免受棕榈酸酯诱导的毒性。我们的结果表明,海藻糖可作为自由基清除剂,减轻受损细胞分泌的过氧化氢的损害。我们还观察到海藻糖通过与质膜相互作用来抵消由棕榈酸酯诱导的膜流动性的变化来保护HepG2细胞。实验结果得到模型细胞膜的分子动力学模拟的支持,该模拟紧密反映了实验条件。进行模拟以了解脂质双层,棕榈酸酯和海藻糖之间的特定相互作用。模拟结果揭示了棕榈酸酯如何诱导细胞膜的生物物理变化以及海藻糖在保护膜结构中的作用的早期阶段。

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