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Characterization of 3D Printed Stretching Devices for Imaging Force Transmission in Live-Cells

机译:用于活细胞成像力传递的3D印刷拉伸装置的特征

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IntroductionCell stretch is a method which can rapidly apply mechanical force through cell-matrix and cell-cell adhesions and can be utilized to better understand underlying biophysical questions related to intracellular force transmission and mechanotransduction.Methods3D printable stretching devices suitable for live-cell fluorescent imaging were designed using finite element modeling and validated experimentally. These devices were then used along with FRET based nesprin-2G force sensitive biosensors as well as live cell fluorescent staining to understand how the nucleus responds to externally applied mechanical force in cells with both intact LINC (linker of nucleoskeleton and cytoskeleton) complex and cells with the LINC complex disrupted using expression of dominant negative KASH protein.ResultsThe devices were shown to provide a larger strain ranges (300% uniaxial and 60% biaxial) than currently available commercial or academic designs we are aware of. Under uniaxial deformation, the deformation of the nucleus of NIH 3T3 cells per unit of imposed cell strain was shown to be approximately 50% higher in control cells compared to cells with a disrupted LINC complex. Under biaxial deformation, MDCK II cells showed permanent changes in the nuclear morphology as well as actin organization upon unloading, indicating that failure, plastic deformation, or remodeling of the cytoskeleton is occurring in response to the applied stretch.ConclusionDevelopment and open distribution of low-cost, 3D-printable uniaxial and biaxial cell stretching devices compatible with live-cell fluorescent imaging allows a wider range of researchers to investigate mechanical influences on biological questions with only a minimal investment of resources.
机译:引入细胞拉伸是一种方法,可以通过细胞 - 基质和细胞 - 细胞粘连快速地施加机械力,并且可以利用以更好地理解与细胞内力传递和机械机构相关的底层生物物理问题..适用于活细胞荧光成像的方法3D可打印拉伸装置是设计使用有限元建模并通过实验验证。然后使用这些装置与基于FRET的NESPRIN-2G力敏感的生物传感器以及活细胞荧光染色,以了解细胞核与完整的LINC(核骨骨骼和细胞骨架)复合物和细胞的完整LINC(接头)对细胞中的外部施加的机械力响应使用显性负kash蛋白的表达破坏的Linc复合物。结果显示出比目前可用的商业或学术设计提供更大的应变范围(300%的单轴和60%的双轴)。在单轴变形下,与具有破坏的Linc复合物的细胞相比,每单位施加的细胞菌株的NIH 3T3细胞的核的变形显示为对照细胞的约50%。在双轴变形下,MDCK II细胞在卸载时显示核形态的永久变化以及肌动蛋白组织,表明响应于所施加的拉伸而发生故障,塑性变形或改造细胞骨架。结论和开放分布低 - 与活细胞荧光成像相容的成本,3D可打印的单轴和双轴电池拉伸装置允许更广泛的研究人员调查对生物学问题的机械影响,只有最小的资源投资。

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