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用于研究帕金森病的强大体外模型?LUHMES细胞和SH-SH5Y细胞。

Robust In Vitro Models for Studying Parkinson's Disease? LUHMES Cells and SH-SH5Y Cells.

作者信息

Keighron Cameron Noah, Avazzedeh Sahar, Quinlan Leo R

机构信息

Cellular Physiology Research Lab, School of Medicine, Department of Physiology, University of Galway, H91W5P7 Galway, Ireland.

CÚRAM SFI Research Centre for Medical Devices, University of Galway, H91W2TY Galway, Ireland.

出版信息

Int J Mol Sci. 2024 Dec 6;25(23):13122. doi: 10.3390/ijms252313122.

Abstract

As our population ages, there is an increased unmet clinical need surrounding neurodegenerative diseases such as Parkinson's disease (PD). To tackle this ever-increasing problem, we must ensure that the cell models that we use to develop therapeutics in vitro are robust, reliable, and replicable. In this study, we compared SH-SY5Y cells with LUHMES cells in response to 6-Hydroxydopamine (6OHDA) and 1-Methyl-4-phenylpyridinium (MPP+), two common Parkinson's insults used in in vitro analysis. Both these cell types have apparent dopaminergic phenotypes, which could aid us in understanding their potential in this race to novel therapies. The LUHMES cells showed consistent dopaminergic (DA) expression through tyrosine hydroxylase (TH) positivity, alongside depleted ATP levels and elevated reactive oxygen species (ROS) production, whereas the SH-SH5Y cells displayed resilience to both chemical insults, raising questions about their utility in accurately modelling PD pathology. Further electrophysiological analysis revealed comparable firing rates and ion channel signalling between both cell types; however, LUHMES cells demonstrated stronger calcium signalling responses, further supporting their use as a more robust PD model. While SH-SY5Y cells showed some adaptability in vitro, their inconsistent DA phenotype and limited response to chemical insults limit their suitability for advanced research, suggesting that LUHMES cells should and must take their place as a hallmark in Parkinson's disease research.

摘要

随着人口老龄化,围绕帕金森病(PD)等神经退行性疾病的未满足临床需求日益增加。为了解决这一日益严重的问题,我们必须确保用于体外开发治疗方法的细胞模型强大、可靠且可重复。在本研究中,我们比较了SH-SY5Y细胞和LUHMES细胞对6-羟基多巴胺(6OHDA)和1-甲基-4-苯基吡啶鎓(MPP+)的反应,这两种物质是体外分析中常用的帕金森病损伤诱导剂。这两种细胞类型都具有明显的多巴胺能表型,这有助于我们了解它们在这场新型疗法竞赛中的潜力。LUHMES细胞通过酪氨酸羟化酶(TH)阳性显示出一致的多巴胺能(DA)表达,同时ATP水平降低,活性氧(ROS)产生增加,而SH-SH5Y细胞对这两种化学损伤均表现出抗性,这引发了人们对其在准确模拟PD病理方面效用的质疑。进一步的电生理分析显示,两种细胞类型之间的放电频率和离子通道信号相当;然而,LUHMES细胞表现出更强的钙信号反应,进一步支持它们作为更强大的PD模型的应用。虽然SH-SY5Y细胞在体外表现出一定的适应性,但它们不一致的DA表型和对化学损伤的有限反应限制了它们在高级研究中的适用性,这表明LUHMES细胞应该而且必须取代它们,成为帕金森病研究的标志性细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77d2/11642316/731c8744dc84/ijms-25-13122-g001.jpg

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