Mammano F, Goodfellow S J, Fountain E
Department of Physiology, School of Medical Sciences, Bristol, UK.
Neuroreport. 1996 Jan 31;7(2):537-42. doi: 10.1097/00001756-199601310-00039.
Tight-seal whole-cell patch clamp recordings were obtained in situ from supporting Hensen's cells within the intact organ of Corti of the adult guinea pig. In normal phosphate buffer solution we estimated 20-50 cells to be coupled by gap junctions to the cell under the patch pipette. In the presence of 1 mM octanol, an uncoupling agent, it was possible to identify an outward current which activated upon depolarization above -20 mV and approached saturation above 70 mV. An inward current was seen with hyperpolarizations below -80 mV. These are broadly similar to the currents of Hensen's cells in vitro. Measured differences of the underlying conductance indicate that the currents are sensitive to the procedure used to isolate cells.
采用紧密封接式全细胞膜片钳记录技术,在成年豚鼠完整的柯蒂氏器内原位记录支持细胞(亨森氏细胞)。在正常磷酸盐缓冲溶液中,我们估计有20 - 50个细胞通过缝隙连接与膜片钳电极下的细胞相连。在存在1 mM辛醇(一种解偶联剂)的情况下,可以识别出一种外向电流,该电流在去极化超过 - 20 mV时激活,并在超过70 mV时接近饱和。当超极化低于 - 80 mV时可观察到内向电流。这些与体外培养的亨森氏细胞的电流大致相似。所测的基础电导差异表明,这些电流对用于分离细胞的操作敏感。