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椎实螺神经元中单个机械敏感通道的延迟激活。

Delayed activation of single mechanosensitive channels in Lymnaea neurons.

作者信息

Small D L, Morris C E

机构信息

Department of Biology, University of Ottawa, Ontario, Canada.

出版信息

Am J Physiol. 1994 Aug;267(2 Pt 1):C598-606. doi: 10.1152/ajpcell.1994.267.2.C598.

Abstract

Some stretch-activated (SA) channels challenged with suction jumps exhibit adaptation, a dynamic behavior that can be overlooked because of its mechanical fragility. In previous studies of neuronal SA K channels, we detected no adaptation, but the protocols used were not designed to detect dynamics. Here, we reproduce the adaptation seen by others in Xenopus SA cationic (Cat) channels but show that, with the same protocol, no adaptation occurs with SA K channels. Instead, SA K channels exhibit a different dynamic behavior, delayed activation. Lymnaea SA K channels subjected to pressure jumps responded after a 1- to 4-s delay with a gradual, rather than abrupt, onset of activation. The delay was pressure dependent and was longer for patches from older cultured neurons. Delayed responses were fragile like SA Cat channel adaptation; they disappeared with repeated stimuli. Cytochalasin D decreased the delay and increased the stretch activation of SA K channels. Unlike SA Cat channel adaptation, which occurs only at hyperpolarized potentials, SA K channel delay was not voltage dependent. We note that once SA Cat and SA K channels are "stripped" of their fragile (cytoskeleton-dependent?) dynamics, however, their gating behaviors show little fundamental difference; both are stretch activatable and have a higher open probability at depolarized potentials.

摘要

一些受吸力阶跃刺激的牵张激活(SA)通道表现出适应性,这是一种由于其机械脆弱性而可能被忽视的动态行为。在先前对神经元SA钾通道的研究中,我们未检测到适应性,但所使用的实验方案并非旨在检测动态变化。在此,我们重现了其他人在非洲爪蟾SA阳离子(Cat)通道中观察到的适应性,但表明使用相同的实验方案时,SA钾通道不会出现适应性。相反,SA钾通道表现出不同的动态行为,即延迟激活。受到压力阶跃刺激的椎实螺SA钾通道在1至4秒的延迟后做出反应,激活开始是逐渐的,而非突然的。这种延迟与压力有关,对于来自培养时间较长的神经元的膜片来说延迟更长。延迟反应像SA Cat通道适应性一样脆弱;它们会随着重复刺激而消失。细胞松弛素D减少了延迟并增加了SA钾通道的牵张激活。与仅在超极化电位下发生的SA Cat通道适应性不同,SA钾通道的延迟不依赖于电压。我们注意到,然而,一旦SA Cat和SA钾通道的脆弱(依赖细胞骨架?)动态变化被“去除”,它们的门控行为几乎没有根本差异;两者都可被牵张激活,并且在去极化电位下具有更高的开放概率。

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