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使用药物筛选微流控芯片检测原代中枢神经系统培养物中的Aβ毒性。

Testing Aβ toxicity on primary CNS cultures using drug-screening microfluidic chips.

作者信息

Ruiz A, Joshi P, Mastrangelo R, Francolini M, Verderio C, Matteoli M

机构信息

Department of Medical Biotechnologies and Translational Medicine, University of Milan, Via L. Vanvitelli 32, 20129 Milan, Italy.

出版信息

Lab Chip. 2014 Aug 7;14(15):2860-6. doi: 10.1039/c4lc00174e. Epub 2014 Jun 10.

Abstract

Open microscale cultures of primary central nervous system (CNS) cells have been implemented in microfluidic chips that can expose the cells to physiological fluidic shear stress conditions. Cells in the chips were exposed to differently aggregated forms of beta-amyloid (Aβ), i.e. conditions mimicking an Alzheimer's Disease environment, and treated with CNS drugs in order to assess the contribution of glial cells during pharmacological treatments. FTY720, a drug approved for the treatment of Multiple Sclerosis, was found to play a marked neuroprotective role in neuronal cultures as well as in microglia-enriched neuronal cultures, preventing neurodegeneration after cell exposure to neurotoxic oligomers of Aβ.

摘要

原发性中枢神经系统(CNS)细胞的开放微尺度培养已在微流控芯片中实现,该芯片可使细胞暴露于生理流体剪切应力条件下。芯片中的细胞暴露于不同聚集形式的β-淀粉样蛋白(Aβ),即模拟阿尔茨海默病环境的条件下,并接受中枢神经系统药物治疗,以评估胶质细胞在药物治疗过程中的作用。FTY720是一种被批准用于治疗多发性硬化症的药物,发现在神经元培养物以及富含小胶质细胞的神经元培养物中具有显著的神经保护作用,可防止细胞暴露于Aβ神经毒性寡聚体后发生神经退行性变。

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