神经突
神经母细胞瘤
细胞生物学
神经退行性变
线粒体
鱼藤酮
细胞分化
SH-SY5Y型
化学
神经毒性
活力测定
细胞培养
细胞
生物
生物化学
体外
毒性
病理
医学
遗传学
有机化学
基因
疾病
作者
Rui F. Simões,Rafaela Ferrão,Margarida Silva,Sónia L. C. Pinho,Lino Ferreira,Paulo J. Oliveira,Teresa Cunha‐Oliveira
标识
DOI:10.1016/j.fct.2021.111967
摘要
Since most models used to study neuronal dysfunction display disadvantages and ethical concerns, a fast and reproducible in vitro model to study mitochondria-related neurodegeneration is required. Here, we optimized and characterized a 3-day retinoic acid-based protocol to differentiate the SH-SY5Y cell line into a neuronal-like phenotype and investigated alterations in mitochondrial physiology and distribution. Differentiation was associated with p21-linked cell cycle arrest and an increase in cell mass and area, possibly associated with the development of neurite-like extensions. Notably, increased expression of mature neuronal markers (neuronal-specific nuclear protein, microtubule-associated protein 2, βIII tubulin and enolase 2) was observed in differentiated cells. Moreover, increased mitochondrial content and maximal area per cell suggests mitochondrial remodeling. To demonstrate that this model is appropriate to study mitochondrial dysfunction, cells were treated for 6 h with mitochondrial toxicants (rotenone, antimycin A, carbonyl cyanide-4-(trifluoromethoxy)phenylhydrazone (FCCP) and 6-hydroxydopamine (6-OHDA)). Differentiated cells were more susceptible to increasing concentrations of FCCP, antimycin A, and rotenone, while 6-OHDA showed a distinct dose-dependent neurotoxicity pattern. Even though differentiated cells did not exhibit a fully mature/differentiated neuronal phenotype, the protocol developed can be used to study neurotoxicity processes, mitochondrial dynamics, and bioenergetic impairment, representing an alternative to study mitochondrial impairment-related pathologies in vitro.
科研通智能强力驱动
Strongly Powered by AbleSci AI