Department of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, The University of Iowa, Iowa City, Iowa 52242, United States.
Department of Chemistry, The University of Iowa, Iowa City, Iowa 52242, United States.
ACS Chem Neurosci. 2020 Mar 18;11(6):840-850. doi: 10.1021/acschemneuro.9b00401. Epub 2020 Feb 28.
Aggregated amyloid beta (Aβ) is widely reported to cause neuronal dystrophy and toxicity through multiple pathways: oxidative stress, disrupting calcium homeostasis, and cytoskeletal dysregulation. The neuro-cytoskeleton is a dynamic structure that reorganizes to maintain cell homeostasis in response to varying soluble and physical cues presented from the extracellular matrix (ECM). Due this relationship between cell health and the ECM, we hypothesize that amyloid toxicity may be directly influenced by physical changes to the ECM (stiffness and dimensionality) through mechanosensitive pathways, and while previous studies demonstrated that Aβ can distort focal adhesion signaling with pathological consequences, these studies do not address the physical contribution from a physiologically relevant matrix. To test our hypothesis that physical cues can adjust Aβ toxicity, SH-SY5Y human neuroblastoma and primary human cortical neurons were plated on soft and stiff, 2D polyacrylamide matrices or suspended in 3D collagen gels. Each cell culture was exposed to escalating concentrations of oligomeric or fibrillated Aβ(1-42) with MTS viability and lactate dehydrogenase toxicity assessed. Actin restructuring was further monitored in live cells by atomic force microscopy nanoindentation, and our results demonstrate that increasing either matrix stiffness or exposure to oligomeric Aβ promotes F-actin polymerization and cell stiffening, while mature Aβ fibrils yielded no apparent cell stiffening and minor toxicity. Moreover, the rounded, softer mechanical phenotype displayed by cells plated onto a compliant matrix also demonstrated a resilience to oligomeric Aβ as noted by a significant recovery of viability when compared to same-dosed cells plated on traditional tissue culture plastic. This recovery was reproduced pharmacologically through inhibiting actin polymerization with cytochalasin D prior to Aβ exposure. These studies indicate that the cell-ECM interface can modify amyloid toxicity in neurons and the matrix-mediated pathways that promote this protection may offer unique targets in amyloid pathologies like Alzheimer's disease.
聚集的淀粉样蛋白β(Aβ)通过多种途径广泛报道导致神经元萎缩和毒性:氧化应激,破坏钙稳态和细胞骨架失调。神经细胞骨架是一种动态结构,它通过细胞外基质(ECM)提供的可溶性和物理线索的变化进行重组,以维持细胞内稳态。由于细胞健康与 ECM 之间的这种关系,我们假设淀粉样蛋白毒性可能直接受到 ECM 物理变化(硬度和维度)的影响,通过机械敏感途径,尽管先前的研究表明 Aβ 可以扭曲病理性的焦点粘附信号,但这些研究并未解决生理相关基质的物理贡献。为了测试我们的假设,即物理线索可以调节 Aβ 毒性,将 SH-SY5Y 人神经母细胞瘤和原代人皮质神经元接种在软和硬的 2D 聚丙烯酰胺基质上或悬浮在 3D 胶原凝胶中。用 MTS 活力和乳酸脱氢酶毒性评估每种细胞培养物中寡聚体或纤维状 Aβ(1-42)的浓度递增暴露。通过原子力显微镜纳米压痕进一步监测活细胞中的肌动蛋白重排,我们的结果表明,增加基质硬度或暴露于寡聚体 Aβ 可促进 F-肌动蛋白聚合和细胞变硬,而成熟的 Aβ 纤维没有产生明显的细胞变硬和较小的毒性。此外,接种在顺应性基质上的细胞表现出圆形、较软的机械表型,这也表明对寡聚体 Aβ 的弹性,与接种在传统组织培养塑料上的相同剂量细胞相比,活力有明显恢复。通过在 Aβ 暴露之前用细胞松弛素 D 抑制肌动蛋白聚合,这种恢复在药理学上得到了重现。这些研究表明,细胞-ECM 界面可以修饰神经元中的淀粉样蛋白毒性,促进这种保护的基质介导途径可能为阿尔茨海默病等淀粉样蛋白病提供独特的靶点。