O'Day P M, Rikmenspoel R
J Cell Sci. 1979 Feb;35:123-38. doi: 10.1242/jcs.35.1.123.
The control of bull spermatozoon flagellar activity has been investigated using direct current injection into the cells through an impaling glass microelectrode. Negative current injection results in a decrease in the flagellar frequency. Flagellar frequencies can be decreased to zero with high negative currents. This current injection response is dependent on the magnesium concentration available to the spermatozoon interior. The current injection response is nearly independent of ATP concentrations. Resistance measurements indicate that the current injection pathway has a resistance of about 200 +/- 300 k omega, and that the current flowing through the cell membrane is not exceedingly large. Measurements of the induced potentials indicate transmembrane potentials during current injection of about -35 +/- 30 mV per microA of injected current. The results are compatible with an active transport process in bull spermatozoa that controls the flagellar activity in response to current injection by decreasing the internal Mg2+ concentrations during the injection of current.
通过一根刺入玻璃微电极向细胞内注入直流电,对公牛精子鞭毛活动的控制进行了研究。注入负电流会导致鞭毛频率降低。高负电流可使鞭毛频率降至零。这种电流注入反应取决于精子内部可利用的镁浓度。电流注入反应几乎与ATP浓度无关。电阻测量表明,电流注入途径的电阻约为200 +/- 300 kΩ,并且流过细胞膜的电流不是非常大。诱导电位的测量表明,在注入电流时,每微安注入电流的跨膜电位约为-35 +/- 30 mV。这些结果与公牛精子中的一种主动运输过程相一致,该过程通过在注入电流时降低内部Mg2+浓度来控制鞭毛活动以响应电流注入。