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Robotic Whole-cell Patch Clamping Based on Three Dimensional Location for Adherent Cells

机译:基于粘附细胞的三维位置的机器人全细胞贴片钳位

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Whole-cell patch clamping is the gold-standard technology for electrical activities recordings of live single cells. To guarantee a high signal-to-noise ratio in recordings, a giga Omega-scale seal (gigaseal) between target cell membrane and the electrode needs to be formed first in whole-cell patch clamping. As lack of precise 3-D location methods for adherent cells, the operators have to roughly position the electrode to contact the target cell, easily resulting in gigaseal formation failures due to cell membrane penetration etc. For the first time, this paper introduced a fully automated whole-cell patch clamping system based on 3-D location for adherent cells under the bright field. First, a defocusing microscopy-based cell segmentation was proposed to locate adherent cell position in horizontal (X-Y) direction. Second, contact detection based on the measured electrode impedance was developed to measure the top surface position of adherent cell in vertical (Z) direction. Based on above work, an automated whole-cell patch clamping process was established. The experimental results on mouse osteoblasts showed that the system was able to successfully locate 94.7% (71/75) of cells with an average error of 0.3 μ m in horizontal direction. In vertical direction, the success rate and the average error of top surface position measurement for cells were 100% (20/20) and less than 4.65%, respectively. With precise 3-D positions of adherent cells, the success rate of whole-cell patch clamping using our method was significantly improved in comparison to manual operation results (70% Vs 40%). The proposed system in this paper provides an effective tool for electrical activities recordings of adherent cells in the future.
机译:全细胞贴片钳制是用于活单细胞的电气活动的金标准技术。为了保证记录中的高信噪比,靶细胞膜和电极之间的GIGA Omega级密封(Gigaseal)需要在全细胞贴片夹紧中形成。由于粘附细胞缺乏精确的3-D定位方法,操作者必须大致定位电极以接触靶细胞,易于导致由于细胞膜渗透等引起的Gigaseal形成失败。这篇论文完全介绍了基于明亮场下的粘附细胞三维位置的自动化全电池贴片系统。首先,提出了一种基于灰度的显微镜的细胞分段,以定位水平(X-Y)方向上的粘附单元位置。其次,开发了基于测量电极阻抗的接触检测以测量垂直(Z)方向上的粘附单元的顶表面位置。基于上述工作,建立了一种自动整体膜片夹紧过程。小鼠成骨细胞的实验结果表明,该系统能够成功地定位94.7%(71/75)的细胞,平均误差在水平方向上为0.3μm。在垂直方向上,细胞顶面位置测量的成功率和平均误差分别为100%(20/20)和小于4.65%。具有粘附细胞的精确3-D位置,与手动操作结果(70%Vs 40%)相比,使用我们的方法的全细胞膜片夹紧的成功率显着改善。本文所提出的制度为未来粘附细胞的电气活动录制提供了有效的工具。

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