Kinosita K, Ashikawa I, Saita N, Yoshimura H, Itoh H, Nagayama K, Ikegami A
Institute of Physical and Chemical Research, Saitama, Japan.
Biophys J. 1988 Jun;53(6):1015-9. doi: 10.1016/S0006-3495(88)83181-3.
Controlled permeability can be conferred to cell membranes by exposing cells to a microsecond electric pulse of sufficient intensity (electroporation). By constructing a fluorescence microimaging system with a submicrosecond time resolution we have been able to resolve temporally and spatially the events in a single cell under a microsecond electric pulse. An enormous membrane conductance, corresponding to a loss of 0.01-0.1% of the membrane area, was observed in those membrane regions where the transmembrane potential induced by the electric pulse exceeded a critical value. The conductance decreased to a low level in a submillisecond after the pulse, leaving a moderately electroporated cell.
通过将细胞暴露于强度足够的微秒级电脉冲(电穿孔),可以赋予细胞膜可控的通透性。通过构建具有亚微秒时间分辨率的荧光显微成像系统,我们得以在微秒级电脉冲下在时间和空间上解析单个细胞内的事件。在电脉冲诱导的跨膜电位超过临界值的那些膜区域中,观察到了巨大的膜电导,这相当于膜面积损失了0.01 - 0.1%。脉冲后亚毫秒内,电导降至低水平,留下一个适度电穿孔的细胞。