Bannai H, Yoshimura M, Takahashi K, Shingyoji C
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo, Tokyo 113-0033, Japan.
J Cell Sci. 2000 Mar;113 ( Pt 5):831-9. doi: 10.1242/jcs.113.5.831.
The changes in the bending pattern of flagella induced by an increased intracellular Ca(2+) concentration are caused by changes in the pattern and velocity of microtubule sliding. However, the mechanism by which Ca(2+) regulates microtubule sliding in flagella has been unclear. To elucidate it, we studied the effects of Ca(2+) on microtubule sliding in reactivated sea urchin sperm flagella that were beating under imposed head vibration. We found that the maximum microtubule sliding velocity obtainable by imposed vibration, which was about 170-180 rad/second in the presence of 250 microM MgATP and <10(-9) M Ca(2+), was decreased by 10(-6)-10(-5) M Ca(2+) by about 15-20%. Similar decrease of the sliding velocity was observed at 54 and 27 microM MgATP. The Ca(2+)-induced decrease of the sliding velocity was due mainly to a decrease in the reverse bend angle. When the plane of beat was artificially rotated by rotating the plane of vibration of the pipette that held the sperm head, the asymmetric bending pattern also rotated at 10(-5) M Ca(2+) as well as at <10(-9) M Ca(2+). The rotation of the bending pattern was observed at MgATP higher than 54 microM ( approximately 100 microM ATP). These results indicate that the Ca(2+)-induced decrease of the sliding velocity is mediated by a rotatable component or components (probably the central pair) at high MgATP, but is not due to specific dynein arms on particular doublets. We further investigated the effects of a mild trypsin treatment and of trifluoperazine on the Ca(2+)-induced decrease in sliding velocity. Axonemes treated for 3 minutes with a low concentration (0.1 microgram/ml) of trypsin beat with a more symmetrical waveform than before the treatment. Also, their microtubule sliding velocity and reverse bend angle were not affected by high Ca(2+) concentrations. Trifluoperazine (25-50 microM) had no effect on the decrease of the sliding velocity in beating flagella at 10(-5) M Ca(2+). However, the flagella that had been 'quiescent' at 10(-4) M Ca(2+) resumed asymmetrical beating following an application of 10-50 microM trifluoperazine. In such beating flagella, both the sliding velocity and the reverse bend angle were close to their respective values at 10(-5) M Ca(2+). Trypsin treatment induced a similar recovery of beating in quiescent flagella at 10(-)(4) M Ca(2+), albeit with a more symmetrical waveform. These results provide first evidence that, at least at ATP concentrations higher than approximately 100 microM, 10(-6)-10(-5) M Ca(2+) decreases the maximum sliding velocity of microtubules in beating flagella through a trypsin-sensitive regulatory mechanism which possibly involves the central pair apparatus. They also suggest that calmodulin may be associated with the mechanism underlying flagellar quiescence induced by 10(-4) M Ca(2+).
细胞内钙离子浓度升高所诱导的鞭毛弯曲模式变化是由微管滑动模式和速度的改变引起的。然而,钙离子调节鞭毛中微管滑动的机制尚不清楚。为了阐明这一机制,我们研究了钙离子对在施加头部振动下摆动的再激活海胆精子鞭毛中微管滑动的影响。我们发现,在存在250微摩尔镁ATP和小于10^(-9)摩尔钙离子的情况下,通过施加振动可获得的最大微管滑动速度约为170 - 180弧度/秒,而10^(-6) - 10^(-5)摩尔钙离子会使其降低约15 - 20%。在54微摩尔和27微摩尔镁ATP时也观察到了类似的滑动速度降低。钙离子诱导的滑动速度降低主要是由于反向弯曲角度的减小。当通过旋转固定精子头部的移液器的振动平面来人为旋转摆动平面时,在10^(-5)摩尔钙离子以及小于10^(-9)摩尔钙离子时,不对称弯曲模式也会旋转。在高于54微摩尔(约100微摩尔ATP)的镁ATP时观察到了弯曲模式的旋转。这些结果表明,在高镁ATP时,钙离子诱导的滑动速度降低是由一个或多个可旋转成分(可能是中央微管对)介导的,而不是由于特定双联体上的特定动力蛋白臂。我们进一步研究了轻度胰蛋白酶处理和三氟拉嗪对钙离子诱导的滑动速度降低的影响。用低浓度(0.1微克/毫升)胰蛋白酶处理3分钟的轴丝摆动波形比处理前更对称。而且,它们的微管滑动速度和反向弯曲角度不受高钙离子浓度的影响。三氟拉嗪(25 - 50微摩尔)对在10^(-5)摩尔钙离子下摆动的鞭毛中滑动速度的降低没有影响。然而,在10^(-4)摩尔钙离子下“静止”的鞭毛在施加10 - 50微摩尔三氟拉嗪后恢复了不对称摆动。在这种摆动的鞭毛中,滑动速度和反向弯曲角度都接近它们在10^(-5)摩尔钙离子时各自的值。胰蛋白酶处理在10^(-4)摩尔钙离子下也诱导了静止鞭毛摆动的类似恢复,尽管波形更对称。这些结果首次证明,至少在ATP浓度高于约100微摩尔时,10^(-6) - 10^(-5)摩尔钙离子通过一种可能涉及中央微管对装置的胰蛋白酶敏感调节机制降低摆动鞭毛中微管的最大滑动速度。它们还表明钙调蛋白可能与10^(-4)摩尔钙离子诱导的鞭毛静止的潜在机制有关。