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A customizable microfluidic platform for medium-throughput modeling of neuromuscular circuits

机译:可定制的微流体平台,用于神经肌肉电路的中吞吐量建模

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摘要

Neuromuscular circuits (NMCs) are vital for voluntary movement, and effective models of NMCs are needed to understand the pathogenesis of, as well as to identify effective treatments for, multiple diseases, including Duchenne's muscular dystrophy and amyotrophic lateral sclerosis. Microfluidics are ideal for recapitulating the central and peripheral compartments of NMCs, but myotubes often detach before functional NMCs are formed. In addition, microfluidic systems are often limited to a single experimental unit, which significantly limits their application in disease modeling and drug discovery. Here, we developed a microfluidic platform (MFP) containing over 100 experimental units, making it suitable for medium-throughput applications. To overcome detachment, we incorporated a reactive polymer surface allowing customization of the environment to culture different cell types. Using this approach, we identified conditions that enable long-term co-culture of human motor neurons and myotubes differentiated from human induced pluripotent stem cells inside our MFP. Optogenetics demonstrated the formation of functional NMCs. Furthermore, we developed a novel application of the rabies tracing assay to efficiently identify NMCs in our MFP. Therefore, our MFP enables large-scale generation and quantification of functional NMCs for disease modeling and pharmacological drug targeting.
机译:神经肌肉电路(NMC)对自愿运动至关重要,需要有效的NMCS态度来理解发病机制,以及鉴定多种疾病的有效治疗,包括Duchenne的肌营养不良和肌营养的侧面硬化。微流体是重新承载NMC的中央和外周舱的理​​想选择,但Myotubes经常在形成功能NMC之前脱离。此外,微流体系统通常限于单一的实验单元,这显着限制了它们在疾病建模和药物发现中的应用。在这里,我们开发了一种微流体平台(MFP),其含有100多个实验单元,适用于中吞吐量应用。为了克服脱离,我们掺入了一种反应性聚合物表面,允许定制环境以培养不同细胞类型。使用这种方法,我们确定了能够在我们的MFP内部的人类诱导的多能干细胞分化的人类运动神经元和肌管的长期共培养。 Optimetics证明了功能性NMC的形成。此外,我们开发了狂犬病追踪测定的新应用,以有效地识别我们的MFP中的NMC。因此,我们的MFP能够为疾病建模和药理药物靶向进行大规模生成和定量功能NMC。

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