Heo Jinseok, Sachs Frederick, Wang Jianbin, Hua Susan Z
Department of Physiology and Biophysics, SUNY-Buffalo, Buffalo, NY 14260, USA.
Cell Physiol Biochem. 2012;30(2):395-406. doi: 10.1159/000339033. Epub 2012 Jul 3.
Using a microfluidic cell volume sensor we measured the change in the cell volume of Madin-Darby Canine Kidney (MDCK) cells induced by shear stress. An increase in shear stress from 0.2 to 2.0 dyn/cm(2) resulted in a volume decrease to a steady state volume ∼ 20 - 30 % smaller than the initial resting cell volume. Independent experiments based on fluorescence quenching confirmed the volume reduction. This shear-induced cell shrinkage was irreversible on the time scale of the experiment (∼ 30 min). Treatment of 0.1 µM Hg(2+) significantly inhibited the volume decrease, suggesting that the shear-induced cell shrinkage is associated with water efflux through aquaporins. The volume decrease cannot be inhibited by 75 mM TEA, 100 µM DIDS, or 100 µM Gd(3+) suggesting that volume reduction is not directly mediated by K(+) and Cl(-)channels that typically function during regulatory volume decrease (RVD), nor is it through cationic stretch-activated ion channels (SACs). The process also appears to be Ca(2+) independent because it was insensitive to intracellular Ca(2+) level. Since cell volume is determined by the intracellular water content, we postulate that the shear induced reductions in cell volume may arise from increased intracellular hydrostatic pressure as the cell is deformed under flow, which promotes the efflux of water. The increase in internal pressure in a deformable object under the flow is supported by the finite element mechanical model.
我们使用微流控细胞体积传感器测量了剪切应力诱导的马-达二氏犬肾(MDCK)细胞的体积变化。剪切应力从0.2 dyn/cm²增加到2.0 dyn/cm²导致细胞体积减小至稳态体积,该稳态体积比初始静息细胞体积小约20 - 30%。基于荧光猝灭的独立实验证实了体积减小。在实验时间尺度(约30分钟)内,这种剪切诱导的细胞收缩是不可逆的。用0.1 µM Hg²⁺处理显著抑制了体积减小,这表明剪切诱导的细胞收缩与通过水通道蛋白的水外流有关。75 mM四乙铵、100 µM 4,4'-二异硫氰酸二苯乙烯-2,2'-二磺酸(DIDS)或100 µM钆离子(Gd³⁺)均不能抑制体积减小,这表明体积减小不是由通常在调节性体积减小(RVD)过程中起作用的钾离子(K⁺)和氯离子(Cl⁻)通道直接介导的,也不是通过阳离子拉伸激活离子通道(SACs)。该过程似乎也与钙离子(Ca²⁺)无关,因为它对细胞内Ca²⁺水平不敏感。由于细胞体积由细胞内水含量决定,我们推测剪切诱导的细胞体积减小可能是由于细胞在流动下变形时细胞内静水压力增加,从而促进了水的外流。流动下可变形物体内部压力的增加得到了有限元力学模型的支持。