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镁离子对眼虫鞭毛活动的电控制

Mg2+-dependent electrical control of flagellar activity in Euglena.

作者信息

Nichols K M, Rikmenspoel R

出版信息

J Cell Sci. 1977 Feb;23:211-25. doi: 10.1242/jcs.23.1.211.

Abstract

When a Euglena gracilis in a Ca2+-containing medium is impaled with a microelectrode, the flagellum is instantly ejected. In a Ca2+-free medium to which 1 mM EGTA has been added, the flagellum remains attached to the organism, but it loses activity upon impalement. Externally added ATP at a concentration of 10 mM will sustain normal flagellar activity (at approximately 20 Hz) of an impaled Euglena. If negative direct current of several tenths of a microamp is injected through the impaling microelectrode, the flagellar activity is stopped or much reduced. When the current injection is turned off the flagellum returns to its initial activity. This cycle can be repeated many times on the same animal, independent of whether Mg2+ is present in the external medium or not. If 1 micrometer of gramicidin is added to Ca2+-free medium containing 1 mM EGTA and 10 mM ATP, the flagellar activity becomes dependent on external Mg2+. Without external Mg2+ no flagellar activity is present after one or two current injection cycles as described above. With 1 mM Mg2+ present in the external medium many cycles (up to 10) can be produced. This Mg2+-dependent flagellar activity shows a smooth dependence on the amount of current injected. Observations taken by high speed cinemicrography show that in the third injection cycle the average frequency of the flagellar motion is 16-3 Hz at 0 muA, is 8 Hz at 0-2 muA, and is approximately 0 at 0-6 muA of negative current. The injection of positive current results in an increase in flagellar frequency dependent on the amount of current injected. The data indicate that the control of motility of Euglena flagella is dependent on an electrically activated Mg2+ pump.

摘要

当用微电极刺入含Ca2+培养基中的纤细裸藻时,鞭毛会立即被弹出。在添加了1 mM乙二醇双四乙酸(EGTA)的无Ca2+培养基中,鞭毛仍附着在生物体上,但在刺入时会失去活性。外部添加浓度为10 mM的ATP可维持被刺入纤细裸藻的正常鞭毛活性(约20 Hz)。如果通过刺入微电极注入几十分之一微安的负直流电,鞭毛活性会停止或大幅降低。当停止注入电流时,鞭毛会恢复其初始活性。这个循环可以在同一只动物上重复多次,与外部培养基中是否存在Mg2+无关。如果向含有1 mM EGTA和10 mM ATP的无Ca2+培养基中添加1微米短杆菌肽,鞭毛活性就会依赖于外部Mg2+。如上述,在没有外部Mg2+的情况下,经过一两个电流注入循环后就没有鞭毛活性了。当外部培养基中存在1 mM Mg2+时,可以产生许多循环(多达10个)。这种依赖Mg2+的鞭毛活性对注入的电流量呈现出平滑的依赖性。高速电影显微镜观察表明,在第三次注入循环中,当负电流为0 μA时,鞭毛运动的平均频率为16 - 3 Hz;当负电流为0 - 2 μA时,平均频率为8 Hz;当负电流为0 - 6 μA时,平均频率约为0。注入正电流会导致鞭毛频率增加,且增加程度依赖于注入的电流量。数据表明,纤细裸藻鞭毛运动的控制依赖于电激活的Mg2+泵。

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