Amrita Center for Nanosciences & Molecular Medicine, Amrita Vishwa Vidyapeetham, Kochi, Kerala 682041, India.
Amrita Center for Nanosciences & Molecular Medicine, Amrita Vishwa Vidyapeetham, Kochi, Kerala 682041, India.
Toxicol In Vitro. 2021 Aug;74:105175. doi: 10.1016/j.tiv.2021.105175. Epub 2021 Apr 16.
The use of gold nanoparticles (AuNps) in applications connected to the peripheral nervous system (PNS) holds much promise in terms of therapeutic and diagnostic strategies. Despite their extensive use, a clear understanding of their effects on neurons and glia in the PNS is lacking. In this study, we set out to examine the effects of AuNps on dorsal root ganglion (DRG) cells, and how such AuNp-exposed cells could in-turn affect neurite differentiation. DRG cultures were exposed to mono-dispersed spherical-shaped AuNps of diameter 24.3 ± 2.3, 109.2 ± 14.7 or 175 ± 19.2 nm at varying concentrations. Cellular uptake and viability were quantified using flow-cytometry. Neurite differentiation was quantified using neurite tracing analysis in PC-12 and DRG neurons exposed to conditioned media derived from AuNp-treated DRG cells. Both neurons and glia were found to internalize AuNps. DRG cell viability was significantly reduced upon treatment with higher concentration of 175 nm sized AuNps, while 24 nm and 109 nm sized AuNps had no effect. Further, conditioned media from AuNp-treated DRG cells produced comparable neurite outgrowth and neurite branching measurement as controls in PC-12 and DRG neurons. DRG cells were quite resilient to AuNp exposure in mild-moderate concentration. AuNp-exposed DRG cells, irrespective of size and concentration range tested, did not affect neuronal differentiation.
金纳米粒子(AuNps)在与周围神经系统(PNS)相关的应用中具有很大的应用前景,无论是在治疗还是诊断策略方面。尽管它们被广泛使用,但对于它们对 PNS 中的神经元和神经胶质细胞的影响,人们的理解还不够清晰。在这项研究中,我们着手研究 AuNps 对背根神经节(DRG)细胞的影响,以及暴露于 AuNp 的细胞如何反过来影响轴突分化。将 DRG 培养物暴露于直径为 24.3±2.3、109.2±14.7 或 175±19.2nm 的单分散球形 AuNps 中,浓度不同。使用流式细胞术定量细胞摄取和活力。使用 PC-12 和 DRG 神经元暴露于源自 AuNp 处理的 DRG 细胞的条件培养基中的神经突追踪分析来定量神经突分化。发现神经元和神经胶质细胞都能内化 AuNps。用更高浓度的 175nm 大小的 AuNps 处理会显著降低 DRG 细胞活力,而 24nm 和 109nm 大小的 AuNps 则没有影响。此外,来自 AuNp 处理的 DRG 细胞的条件培养基在 PC-12 和 DRG 神经元中产生与对照相当的神经突生长和神经突分支测量值。DRG 细胞在轻度至中度浓度的 AuNp 暴露下具有很强的抵抗力。无论大小和测试浓度范围如何,暴露于 AuNp 的 DRG 细胞都不会影响神经元分化。