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High-throughput microfluidic micropipette aspiration device to probe time-scale dependent nuclear mechanics in intact cells

机译:高吞吐量微流体微量探针吸入装置,探测完整细胞中的时间级依赖性核电机构

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The mechanical properties of the cell nucleus are increasingly recognized as critical in many biological processes. The deformability of the nucleus determines the ability of immune and cancer cells to migrate through tissues and across endothelial cell layers, and changes to the mechanical properties of the nucleus can serve as novel biomarkers in processes such as cancer progression and stem cell differentiation. However, current techniques to measure the viscoelastic nuclear mechanical properties are often time consuming, limited to probing one cell at a time, or require expensive, highly specialized equipment. Furthermore, many current assays do not measure time-dependent properties, which are characteristic of viscoelastic materials. Here, we present an easy-to-use microfluidic device that applies the well-established approach of micropipette aspiration, adapted to measure many cells in parallel. The device design allows rapid loading and purging of cells for measurements, and minimizes clogging by large particles or clusters of cells. Combined with a semi-automated image analysis pipeline, the microfluidic device approach enables significantly increased experimental throughput. We validated the experimental platform by comparing computational models of the fluid mechanics in the device with experimental measurements of fluid flow. In addition, we conducted experiments on cells lacking the nuclear envelope protein lamin A/C and wild-type controls, which have well-characterized nuclear mechanical properties. Fitting time-dependent nuclear deformation data to power law and different viscoelastic models revealed that loss of lamin A/C significantly altered the elastic and viscous properties of the nucleus, resulting in substantially increased nuclear deformability. Lastly, to demonstrate the versatility of the devices, we characterized the viscoelastic nuclear mechanical properties in a variety of cell lines and experimental model systems, including human skin fibroblasts from an individual with a mutation in the lamin gene associated with dilated cardiomyopathy, healthy control fibroblasts, induced pluripotent stem cells (iPSCs), and human tumor cells. Taken together, these experiments demonstrate the ability of the microfluidic device and automated image analysis platform to provide robust, high throughput measurements of nuclear mechanical properties, including time-dependent elastic and viscous behavior, in a broad range of applications.
机译:细胞核的力学性质在许多生物过程中越来越担心为关键。细胞核的可变形性决定了免疫和癌细胞通过组织和跨内皮细胞层迁移的能力,并且对细胞核的力学性质的变化可以作为癌症进展和干细胞分化等方法中的新型生物标志物。然而,测量粘弹性核力学性能的当前技术通常是耗时的,仅限于一次探测一个电池,或者需要昂贵的高度专业化的设备。此外,许多电流测定不能测量时间依赖性的性质,这是粘弹性材料的特征。在这里,我们介绍了一种易于使用的微流体装置,该装置应用微型仪吸入的良好方法,适于平行测量许多细胞。器件设计允许快速加载和吹扫细胞进行测量,并最大限度地减少由大颗粒或细胞簇堵塞。结合半自动图像分析管道,微流体装置方法能够显着提高实验过程。通过将装置中的流体力学计算模型与实验测量的流体流程进行比较,我们通过对实验模型进行了验证了实验平台。此外,我们对缺乏核包膜蛋白蛋白-A / C和野生型对照进行的细胞进行了实验,具有良好表征的核力学性能。将时间依赖的核变形数据赋予权力法和不同的粘弹性模型,显示Lamin A / C的损失显着改变了核的弹性和粘性特性,从而显着增加了核变形性。最后,为了证明这些装置的多功能性,我们在各种细胞系和实验模型系统中表征了粘弹性核力学性能,包括来自具有与扩张的心肌病,健康对照成纤维细胞相关的脉冲基因突变的人类皮肤成纤维细胞,诱导多能干细胞(IPSC)和人肿瘤细胞。这些实验一起展示了微流体装置和自动图像分析平台提供了鲁棒,高通量测量的核力学性能,包括时间依赖性弹性和粘性行为,在广泛的应用中。

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