Iwasa K H, Adachi M
Biophysics Section, LCB, National Institute of Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland 20892-0922, USA.
Biophys J. 1997 Jul;73(1):546-55. doi: 10.1016/S0006-3495(97)78092-5.
The outer hair cell of the mammalian cochlea has a unique motility directly dependent on the membrane potential. Examination of the force generated by the cell is an important step in clarifying the detailed mechanism as well as the biological importance of this motility. We performed a series of experiments to measure force in which an elastic probe was attached to the cell near the cuticular plate and the cell was driven with voltage pulses delivered from a patch pipette under whole-cell voltage clamp. The axial stiffness was also determined with the same cell by stretching it with the patch pipette. The isometric force generated by the cell is around 0.1 nN/mV, somewhat smaller than 0.15 nN/mV, predicted by an area motor model based on mechanical isotropy, but larger than in earlier reports in which the membrane potential was not controlled. The axial stiffness obtained, however, was, on average, 510 nN per unit strain, about half of the value expected from the mechanical isotropy of the membrane. We extended the area motor theory incorporating mechanical orthotropy to accommodate the axial stiffness determined. The force expected from the orthotropic model was within experimental uncertainties.
哺乳动物耳蜗的外毛细胞具有独特的能动性,该能动性直接依赖于膜电位。检测细胞产生的力是阐明这种能动性详细机制及其生物学重要性的重要一步。我们进行了一系列实验来测量力,具体做法是将一个弹性探针附着在靠近表皮板的细胞上,并在全细胞电压钳制下用膜片吸管施加的电压脉冲驱动细胞。还用同一个细胞通过膜片吸管拉伸来测定轴向刚度。细胞产生的等长力约为0.1 nN/mV,略小于基于机械各向同性的面积运动模型预测的0.15 nN/mV,但大于早期未控制膜电位时的报告中的数值。然而,所测得的轴向刚度平均为每单位应变510 nN,约为根据膜的机械各向同性预期值的一半。我们扩展了面积运动理论,纳入了机械正交各向异性以适应所测定的轴向刚度。正交各向异性模型预期的力在实验误差范围内。