State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology , Sichuan University , Chengdu 610021 , China.
ACS Appl Mater Interfaces. 2018 Jul 18;10(28):23682-23692. doi: 10.1021/acsami.8b07827. Epub 2018 Jun 29.
Accumulating evidence supports the abnormal deposition of amyloid β-peptide (Aβ) as the main cause of Alzheimer's disease (AD). Therefore, fighting against the formation, deposition, and toxicity of Aβ is a basic strategy for the treatment of AD. In the process of in vitro nerve cell culture, screening out drugs that can antagonize a series of toxic reactions caused by β-amyloid deposition has become an effective method for the follow-up treatment of AD. Our previous studies showed that tetrahedral DNA nanostructures (TDNs) had good biocompatibility and had some positive effects on the biological behavior of cells. In this study, the main aim of our work was to explore the effects and potential mechanism of TDNs in protecting neuronal PC12 cells from the toxicity of Aβ. Our study demonstrated that TDNs can protect and rescue PC12 cell death through Aβ25-35-induced PC12 cell apoptosis. Further studies showed that TDNs significantly improved the apoptosis by affecting the abnormal cell cycle, restoring abnormal nuclear morphology and caspase activity. Western blot analysis showed that TDNs could prevent the damage caused by Aβ deposition by activating the ERK1/2 pathway and thus be a potential therapeutic agent with a neuroprotective effect in Alzheimer's disease. Our finding provides a potential application of TDNs in the prevention and treatment of AD.
越来越多的证据支持淀粉样 β-肽(Aβ)的异常沉积是阿尔茨海默病(AD)的主要原因。因此,对抗 Aβ的形成、沉积和毒性是治疗 AD 的基本策略。在体外神经细胞培养过程中,筛选出能拮抗β-淀粉样蛋白沉积引起的一系列毒性反应的药物已成为 AD 后续治疗的有效方法。我们之前的研究表明,四面体 DNA 纳米结构(TDN)具有良好的生物相容性,并对细胞的生物学行为有一定的积极影响。在这项研究中,我们工作的主要目的是探讨 TDN 在保护神经元 PC12 细胞免受 Aβ毒性方面的作用及其潜在机制。我们的研究表明,TDN 可以通过 Aβ25-35 诱导的 PC12 细胞凋亡来保护和挽救 PC12 细胞死亡。进一步的研究表明,TDN 通过影响异常细胞周期、恢复异常核形态和半胱天冬酶活性显著改善了细胞凋亡。Western blot 分析表明,TDN 可以通过激活 ERK1/2 通路来防止 Aβ沉积引起的损伤,从而成为一种具有神经保护作用的治疗阿尔茨海默病的潜在药物。我们的发现为 TDN 在预防和治疗 AD 方面提供了一种潜在的应用。