神经生长因子分化的 pc12 细胞的形态计量和荧光分析

Simge Ünay, Ferhat Şi̇ri̇nyildiz
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摘要

目的 PC12 是一种大鼠嗜铬细胞瘤细胞系。在使用神经生长因子(NGF)培养时,这些细胞会发生特征性分化。根据 NGF 的剂量,神经元延伸的长度会发生变化。由于这种分化特性,这种细胞被用于神经科学和病理生理疾病的建模,如阿尔茨海默氏症、帕金森氏症和肌萎缩侧索硬化症。 然而,显示 NGF 对 PC12 细胞中形成的神经元延伸的影响的文献研究非常有限。本研究旨在探讨 NGF 对神经元延伸和细胞活力的影响,具体取决于剂量和培养时间。 材料与方法 在本研究中,PC12 细胞分别与 50 ng/ml 和 100 ng/ml NGF 培养 3、6 和 7 天。计算培养细胞的神经元突起长度和死细胞比率。 结果 结果显示,神经元延伸长度和死细胞比率随 NGF 剂量和培养时间的不同而增加。比较 NGF 培养时间,发现 50 ng/ml NGF 6 天组和 100 ng/ml NGF 3 天组之间没有差异。 结论 在对各实验组的死细胞比率和神经元延伸大小进行评估后,认为 100 ng/ml NGF 和 3 天孵育时间是 PC12 细胞分化的理想参数。
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SİNİR BÜYÜME FAKTÖRÜ İLE FARKLILAŞTIRILMIŞ PC12 HÜCRELERİNİN MORFOMETRİK VE FLORESANS ANALİZİ
Objective PC12 is a rat pheochromocytoma cell line. These cells characteristically undergo differentiation when cultured with nerve growth factor (NGF). Depending on the dose of NGF, the length of neurite extensions changes. Thanks to this differentiation property, the cells are used in neuroscience and in modeling pathophysiological diseases such as Alzheimer's, Parkinson's, and Amyotrophic Lateral Sclerosis. However, literature studies showing the effect of NGF on neurite extensions formed in PC12 cells are very limited. This study aimed to investigate the effect of NGF on neurite extensions and cell viability depending on dose and incubation time. Materials and Methods In this study, PC12 cells were incubated with 50 ng/ml and 100 ng/ml NGF for 3, 6 and 7 days. The lengths of neurite outgrowths and dead cell ratios were calculated in incubated cells. Results The results showed that the length of neurite extensions and dead cell ratio increased depending on NGF doses and incubation time. When NGF incubation times were compared, no difference was found between 50 ng/ml NGF 6 days and 100 ng/ml NGF 3 days groups. Conclusion When the dead cell ratios and sizes of neurite extensions in the experimental groups are evaluated, it is thought that 100 ng/ml NGF and 3 days incubation time parameters are ideal for PC12 cell differentiation.
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