中间电导Ca2+激活的钾通道通过与拉伸激活的非选择性阳离子通道的功能偶联而激活

T. Numata, Kaori Sato-Numata, M. Yoshino
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摘要

局部离子通道的协同门控范围从微调肌肉细胞的兴奋-收缩耦合到控制心脏的起搏活动。由肌肉收缩引起的膜变形激活拉伸激活(SA)阳离子通道。随后的Ca2+内流激活空间局部Ca2+敏感的K+通道,以微调自发肌肉收缩。为了表征内源性表达的中间电导Ca2+活化钾(IK)通道,并评估导致IK通道活性的细胞外Ca2+源的功能相关性,我们对蟋蟀输卵管肌细胞进行了膜片钳技术,并记录了单通道数据。在这项研究中,我们首先研究了通过添加细胞外Ba2+来区分IK通道和内源性表达的大电导Ca2+活化钾(BK)通道。IK通道的单通道电导为62 pS,其活性随细胞内Ca2+浓度的增加而增加,但不依赖于电压。这些结果表明IK通道在蟋蟀输卵管肌细胞中是内源性表达的。其次,研究了激活IK通道的Ca2+内流途径。细胞外Ca2+的缺乏或Gd3+的存在会消除IK通道的活性。最后,我们研究了SA和IK通道之间的接近性。去除细胞外Ca2+,在移液管中给Ca2+到显微镜区域,并应用膜拉伸刺激增加SA通道活性,其次是IK通道活性。膜拉伸诱导的SA与IK通道活性呈正相关。然而,在移液管中没有Ca2+的情况下,没有观察到IK通道活性的出现及其对膜机械拉伸的响应增加。这些结果强烈表明,IK通道在蟋蟀输卵管肌细胞中是内源性表达的,并且IK通道的活性受邻近SA通道活性的调节。综上所述,SA和IK通道之间的功能耦合可能是自发节律性收缩的分子基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermediate conductance Ca2+-activated potassium channels are activated by functional coupling with stretch-activated nonselective cation channels in cricket myocytes
Cooperative gating of localized ion channels ranges from fine-tuning excitation–contraction coupling in muscle cells to controlling pace-making activity in the heart. Membrane deformation resulting from muscle contraction activates stretch-activated (SA) cation channels. The subsequent Ca2+ influx activates spatially localized Ca2+-sensitive K+ channels to fine-tune spontaneous muscle contraction. To characterize endogenously expressed intermediate conductance Ca2+-activated potassium (IK) channels and assess the functional relevance of the extracellular Ca2+ source leading to IK channel activity, we performed patch-clamp techniques on cricket oviduct myocytes and recorded single-channel data. In this study, we first investigated the identification of IK channels that could be distinguished from endogenously expressed large-conductance Ca2+-activated potassium (BK) channels by adding extracellular Ba2+. The single-channel conductance of the IK channel was 62 pS, and its activity increased with increasing intracellular Ca2+ concentration but was not voltage-dependent. These results indicated that IK channels are endogenously expressed in cricket oviduct myocytes. Second, the Ca2+ influx pathway that activates the IK channel was investigated. The absence of extracellular Ca2+ or the presence of Gd3+ abolished the activity of IK channels. Finally, we investigated the proximity between SA and IK channels. The removal of extracellular Ca2+, administration of Ca2+ to the microscopic region in a pipette, and application of membrane stretching stimulation increased SA channel activity, followed by IK channel activity. Membrane stretch-induced SA and IK channel activity were positively correlated. However, the emergence of IK channel activity and its increase in response to membrane mechanical stretch was not observed without Ca2+ in the pipette. These results strongly suggest that IK channels are endogenously expressed in cricket oviduct myocytes and that IK channel activity is regulated by neighboring SA channel activity. In conclusion, functional coupling between SA and IK channels may underlie the molecular basis of spontaneous rhythmic contractions.
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