Cell Biology, Neurosciences and Experimental Myology Laboratory, Victor Babeș Institute of Pathology, 050096 Bucharest, Romania.
Department of Clinical Neurosciences, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
J Integr Neurosci. 2023 Jan 16;22(1):20. doi: 10.31083/j.jin2201020.
The SH-SY5Y cell line is a simple and inexpensive experimental model for studying Parkinson disease (PD). This experimental model is a useful tool for elucidating pathophysiological mechanisms of PD and in the development of new pharmacological therapies. In this review, we aim to summarize current protocols for SH-SY5Y cell culturing and differentiation and PD experimental designs derived from the SH-SY5Y cell line. The most efficient protocol for differentiation of the SH-SY5Y cell line into dopaminergic neurons seems to be the addition of retinoic acid to the growth medium, followed by 12-O-tetradecanoylphorbol-13-acetate (TPA) addition in a low concentration of fetal bovine serum. PD pathological changes, such as neuronal apoptosis and the intraneuronal alpha-synuclein aggregation, can be reproduced in the SH-SY5Y cell line either by the use of neurotoxic agents [such as rotenone, 1-methyl-4-phenylpyridinium (MPP+), 6-hydroxydopamine] or by genetic modification (transfection of the alpha-synuclein wild-type or mutant gene, genetic manipulation of other genes involved in PD). In addition, compounds with a potential neuroprotective role may be tested on neurotoxicity-induced SH-SY5Y models. The cell line can also be used for testing PD pathophysiological mechanisms such as the prion-like neuronal transmission of alpha-synuclein or the microbiota influence in PD. In conclusion, the use of the SH-SY5Y cell line represents a basic but consistent first step in experiments related to PD, but which must be followed by the confirmation of the results through more complex and experimental models.
SH-SY5Y 细胞系是研究帕金森病 (PD) 的简单且经济的实验模型。该实验模型是阐明 PD 病理生理机制和开发新的药理学治疗方法的有用工具。在这篇综述中,我们旨在总结 SH-SY5Y 细胞培养和分化的当前方案以及源自 SH-SY5Y 细胞系的 PD 实验设计。将 SH-SY5Y 细胞系分化为多巴胺能神经元的最有效方案似乎是在生长培养基中添加视黄酸,然后在低浓度胎牛血清中添加 12-O-十四烷酰佛波醇-13-乙酸酯 (TPA)。PD 病理变化,如神经元凋亡和细胞内 α-突触核蛋白聚集,可通过使用神经毒性剂 [如鱼藤酮、1-甲基-4-苯基吡啶 (MPP+)、6-羟多巴胺] 或遗传修饰 (转染 α-突触核蛋白野生型或突变基因、遗传操纵参与 PD 的其他基因) 在 SH-SY5Y 细胞系中再现。此外,具有潜在神经保护作用的化合物可以在神经毒性诱导的 SH-SY5Y 模型上进行测试。该细胞系还可用于测试 PD 病理生理机制,如 α-突触核蛋白的类朊病毒神经元传递或 PD 中的微生物组影响。总之,SH-SY5Y 细胞系的使用代表了与 PD 相关实验的基本但一致的第一步,但必须通过更复杂和实验模型来确认结果。