Sato M, Theret D P, Wheeler L T, Ohshima N, Nerem R M
Department of Biomedical Engineering, University of Tsukuba, Ibaraki, Japan.
J Biomech Eng. 1990 Aug;112(3):263-8. doi: 10.1115/1.2891183.
The viscoelastic deformation of porcine aortic endothelial cells grown under static culture conditions was measured using the micropipette technique. Experiments were conducted both for control cells (mechanically or trypsin detached from the substrate) and for cells in which cytoskeletal elements were disrupted by cytochalasin B or colchicine. The time course of the aspirated length into the pipette was measured after applying a stepwise increase in aspiration pressure. To analyze the data, a standard linear viscoelastic half-space model of the endothelial cell was used. The aspirated length was expressed as an exponential function of time. The actin microfilaments were found to be the major cytoskeletal component determining the viscoelastic response of endothelial cells grown in static culture.
使用微量移液器技术测量了在静态培养条件下生长的猪主动脉内皮细胞的粘弹性变形。对对照细胞(通过机械方法或用胰蛋白酶从基质上分离)以及用细胞松弛素B或秋水仙碱破坏细胞骨架成分的细胞都进行了实验。在逐步增加抽吸压力后,测量了吸进移液器的长度随时间的变化过程。为了分析数据,使用了内皮细胞的标准线性粘弹性半空间模型。吸进的长度表示为时间的指数函数。发现肌动蛋白微丝是决定静态培养中生长的内皮细胞粘弹性反应的主要细胞骨架成分