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皮质神经元在3D打印增强基质中形成功能性神经网络。

Cortical Neurons form a Functional Neuronal Network in a 3D Printed Reinforced Matrix.

作者信息

Janzen Dieter, Bakirci Ezgi, Wieland Annalena, Martin Corinna, Dalton Paul D, Villmann Carmen

机构信息

Institute for Clinical Neurobiology, University Hospital Würzburg, Versbacherstr. 5, Würzburg, 97078, Germany.

Department of Functional Materials in Medicine and Dentistry and Bavarian Polymer Institute, University Hospital Würzburg, Pleicherwall 2, Würzburg, 97070, Germany.

出版信息

Adv Healthc Mater. 2020 May;9(9):e1901630. doi: 10.1002/adhm.201901630. Epub 2020 Mar 17.

Abstract

Impairments in neuronal circuits underly multiple neurodevelopmental and neurodegenerative disorders. 3D cell culture models enhance the complexity of in vitro systems and provide a microenvironment closer to the native situation than with 2D cultures. Such novel model systems will allow the assessment of neuronal network formation and their dysfunction under disease conditions. Here, mouse cortical neurons are cultured from embryonic day E17 within in a fiber-reinforced matrix. A soft Matrigel with a shear modulus of 31 ± 5.6 Pa is reinforced with scaffolds created by melt electrowriting, improving its mechanical properties and facilitating the handling. Cortical neurons display enhance cell viability and the neuronal network maturation in 3D, estimated by staining of dendrites and synapses over 21 days in vitro, is faster in 3D compared to 2D cultures. Using functional readouts with electrophysiological recordings, different firing patterns of action potentials are observed, which are absent in the presence of the sodium channel blocker, tetrodotoxin. Voltage-gated sodium currents display a current-voltage relationship with a maximum peak current at -25 mV. With its high customizability in terms of scaffold reinforcement and soft matrix formulation, this approach represents a new tool to study neuronal networks in 3D under normal and, potentially, disease conditions.

摘要

神经元回路的损伤是多种神经发育和神经退行性疾病的基础。3D细胞培养模型提高了体外系统的复杂性,并提供了比2D培养更接近自然状态的微环境。这种新型模型系统将有助于评估疾病条件下神经网络的形成及其功能障碍。在此,从小鼠胚胎第17天的皮质神经元在纤维增强基质中进行培养。通过熔体电写技术制备的支架增强了剪切模量为31±5.6 Pa的软基质胶,改善了其机械性能并便于操作。皮质神经元在3D环境中显示出更高的细胞活力,通过对体外21天的树突和突触进行染色评估,3D环境中神经网络的成熟速度比2D培养更快。使用电生理记录的功能读数,可以观察到不同的动作电位发放模式,而在存在钠通道阻滞剂河豚毒素的情况下则不存在这些模式。电压门控钠电流显示出电流-电压关系,在-25 mV时具有最大峰值电流。由于其在支架增强和软基质配方方面具有高度可定制性,这种方法代表了一种在正常以及潜在疾病条件下研究3D神经网络的新工具。

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