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帕金森病研究中的SH-SY5Y细胞系:一项系统综述。

The SH-SY5Y cell line in Parkinson's disease research: a systematic review.

作者信息

Xicoy Helena, Wieringa Bé, Martens Gerard J M

机构信息

Department of Cell Biology, Radboud Institute for Molecular Life Sciences (RIMLS), Radboudumc, Nijmegen, The Netherlands.

Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.

出版信息

Mol Neurodegener. 2017 Jan 24;12(1):10. doi: 10.1186/s13024-017-0149-0.

Abstract

Parkinson's disease (PD) is a devastating and highly prevalent neurodegenerative disease for which only symptomatic treatment is available. In order to develop a truly effective disease-modifying therapy, improvement of our current understanding of the molecular and cellular mechanisms underlying PD pathogenesis and progression is crucial. For this purpose, standardization of research protocols and disease models is necessary. As human dopaminergic neurons, the cells mainly affected in PD, are difficult to obtain and maintain as primary cells, current PD research is mostly performed with permanently established neuronal cell models, in particular the neuroblastoma SH-SY5Y lineage. This cell line is frequently chosen because of its human origin, catecholaminergic (though not strictly dopaminergic) neuronal properties, and ease of maintenance. However, there is no consensus on many fundamental aspects that are associated with its use, such as the effects of culture media composition and of variations in differentiation protocols. Here we present the outcome of a systematic review of scientific articles that have used SH-SY5Y cells to explore PD. We describe the cell source, culture conditions, differentiation protocols, methods/approaches used to mimic PD and the preclinical validation of the SH-SY5Y findings by employing alternative cellular and animal models. Thus, this overview may help to standardize the use of the SH-SY5Y cell line in PD research and serve as a future user's guide.

摘要

帕金森病(PD)是一种具有破坏性且极为常见的神经退行性疾病,目前仅有对症治疗方法。为了开发真正有效的疾病修饰疗法,加深我们对PD发病机制和进展背后分子及细胞机制的当前理解至关重要。为此,研究方案和疾病模型的标准化很有必要。由于人类多巴胺能神经元(PD中主要受影响的细胞)难以作为原代细胞获取和维持,当前的PD研究大多使用永久建立的神经元细胞模型,特别是神经母细胞瘤SH-SY5Y谱系。选择该细胞系是因其源自人类、具有儿茶酚胺能(尽管并非严格的多巴胺能)神经元特性且易于培养。然而,在与其使用相关的许多基本方面尚无共识,例如培养基成分的影响以及分化方案的差异。在此,我们展示了对使用SH-SY5Y细胞探索PD的科学文章进行系统综述的结果。我们描述了细胞来源、培养条件、分化方案、用于模拟PD的方法/途径以及通过采用替代细胞和动物模型对SH-SY5Y研究结果进行的临床前验证。因此,本综述可能有助于规范SH-SY5Y细胞系在PD研究中的使用,并作为未来用户指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/163d/5259880/3507763a5198/13024_2017_149_Fig1_HTML.jpg

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