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Cell volume and membrane stretch independently control K+ channel activity

机译:细胞体积和膜拉伸独立控制K +通道活性

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摘要

A number of potassium channels including members of the KCNQ family and the Ca2+ activated IK and SK, but not BK, are strongly and reversibly regulated by small changes in cell volume. It has been argued that this general regulation is mediated through sensitivity to changes in membrane stretch. To test this hypothesis we have studied the regulation of KCNQ1 and BK channels after expression in Xenopus oocytes. Results from cell-attached patch clamp studies (∼50 μm2 macropatches) in oocytes expressing BK channels demonstrate that the macroscopic volume-insensitive BK current increases with increasing negative hydrostatic pressure (suction) applied to the pipette. Thus, at a pipette pressure of −5.0 ± 0.1 mmHg the increase amounted to 381 ± 146% (mean ±s.e.m., n= 6, P < 0.025). In contrast, in oocytes expressing the strongly volume-sensitive KCNQ1 channel, the current was not affected by membrane stretch. The results indicate that (1) activation of BK channels by local membrane stretch is not mimicked by membrane stress induced by cell swelling, and (2) activation of KCNQ1 channels by cell volume increase is not mediated by local tension in the cell membrane. We conclude that stretch and volume sensitivity can be considered two independent regulatory mechanisms.
机译:细胞大小的微小变化强烈且可逆地调节了钾通道,包括KCNQ家族成员和Ca 2 + 活化的IK和SK,但不包括BK。有人认为,这种一般调节是通过对膜拉伸变化的敏感性介导的。为了验证该假设,我们研究了在爪蟾卵母细胞中表达后KCNQ1和BK通道的调控。在表达BK通道的卵母细胞中,细胞附着膜片钳研究(〜50μm 2 巨片)的结果表明,对吸液管施加的负静水压(吸力),对体积不敏感的宏观BK电流会增加。因此,在-5.0±0.1 mmHg的移液器压力下,增加量为381±146%(平均±s.e.m.,n = 6,P <0.025)。相反,在表达强烈体积敏感的KCNQ1通道的卵母细胞中,电流不受膜拉伸的影响。结果表明:(1)细胞膨胀诱导的膜应力不能模拟通过局部膜拉伸引起的BK通道激活;(2)细胞体积增加所导致的KCNQ1通道激活不是通过细胞膜中的局部张力介导的。我们得出结论,拉伸和体积敏感性可以被认为是两个独立的调节机制。

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