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Humic Acid Increases Amyloid β-Induced Cytotoxicity by Induction of ER Stress in Human SK-N-MC Neuronal Cells

机译:腐殖酸通过诱导人SK-N-MC神经元细胞内质网应激增加淀粉样β诱导的细胞毒性

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摘要

Humic acid (HA) is a possible etiological factor associated with for several vascular diseases. It is known that vascular risk factors can directly increase the susceptibility to Alzheimer’s disease (AD), which is a neurodegenerative disorder due to accumulation of amyloid β (Aβ) peptide in the brain. However, the role that HA contributes to Aβ-induced cytotoxicity has not been demonstrated. In the present study, we demonstrate that HA exhibits a synergistic effect enhancing Aβ-induced cytotoxicity in cultured human SK-N-MC neuronal cells. Furthermore, this deterioration was mediated through the activation of endoplasmic reticulum (ER) stress by stimulating PERK and eIF2α phosphorylation. We also observed HA and Aβ-induced cytotoxicity is associated with mitochondrial dysfunction caused by down-regulation of the Sirt1/PGC1α pathway, while in contrast, treating the cells with the ER stress inhibitor Salubrinal, or over-expression of Sirt1 significantly reduced loss of cell viability by HA and Aβ. Our findings suggest a new mechanism by which HA can deteriorate Aβ-induced cytotoxicity through modulation of ER stress, which may provide significant insights into the pathogenesis of AD co-occurring with vascular injury.
机译:腐殖酸(HA)是可能与多种血管疾病相关的病因。众所周知,血管危险因素可以直接增加对阿尔茨海默氏病(AD)的敏感性,该病是由于淀粉样蛋白β(Aβ)肽在大脑中积累而引起的神经退行性疾病。然而,尚未证明HA有助于Aβ诱导的细胞毒性。在本研究中,我们证明HA在培养的人SK-N-MC神经元细胞中表现出增强Aβ诱导的细胞毒性的协同作用。此外,这种恶化是通过刺激PERK和eIF2α磷酸化通过激活内质网(ER)介导的。我们还观察到HA和Aβ诱导的细胞毒性与Sirt1 /PGC1α通路的下调引起的线粒体功能障碍有关,而与此相反,用ER应激抑制剂Salubrinal处理细胞或过度表达Sirt1则可减少线粒体功能障碍。 HA和Aβ对细胞的生存力。我们的发现表明,HA可以通过调节ER应激而恶化Aβ诱导的细胞毒性的新机制,这可能为与血管损伤同时发生的AD发病机理提供重要见解。

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