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压力和超声通过增加膜张力激活机械敏感的TRAAK K通道。

Pressure and ultrasound activate mechanosensitive TRAAK K channels through increased membrane tension.

作者信息

Sorum Ben, Docter Trevor, Panico Vincent, Rietmeijer Robert A, Brohawn Stephen G

机构信息

Department of Molecular & Cell Biology, University of California Berkeley, Berkeley, California 94720, USA.

Helen Wills Neuroscience Institute, University of California Berkeley, Berkeley, California 94720, USA.

出版信息

bioRxiv. 2023 Jan 12:2023.01.11.523644. doi: 10.1101/2023.01.11.523644.

Abstract

TRAAK is a mechanosensitive two-pore domain K (K2P) channel found in nodes of Ranvier within myelinated axons. It displays low leak activity at rest and is activated up to one hundred-fold by increased membrane tension. Structural and functional studies have led to physical models for channel gating and mechanosensitivity, but no quantitative analysis of channel activation by tension has been reported. Here, we use simultaneous patch-clamp recording and fluorescent imaging to determine the tension response characteristics of TRAAK. TRAAK shows high sensitivity and a broad response to tension spanning nearly the entire physiologically relevant tension range. This graded response profile distinguishes TRAAK from similarly low-threshold mechanosensitive channels Piezo1 and MscS, which activate in a step-like fashion over a narrow tension range. We further use patch imaging to show that ultrasonic activation of TRAAK and MscS is due to increased membrane tension. Together, these results provide mechanistic insight into TRAAK tension gating, a framework for exploring the role of mechanosensitive K channels at nodes of Ranvier, and biophysical context for developing ultrasound as a mechanical stimulation technique for neuromodulation.

摘要

TRAAK是一种机械敏感的双孔结构域钾离子(K2P)通道,存在于有髓轴突的郎飞结中。它在静息时表现出低泄漏活性,并在膜张力增加时被激活达100倍。结构和功能研究已经得出了通道门控和机械敏感性的物理模型,但尚未有关于通道被张力激活的定量分析报道。在这里,我们使用膜片钳记录和荧光成像同步技术来确定TRAAK的张力反应特性。TRAAK对张力表现出高敏感性和广泛的反应,几乎涵盖了整个生理相关的张力范围。这种分级反应模式将TRAAK与同样低阈值的机械敏感通道Piezo1和MscS区分开来,后者在狭窄的张力范围内以阶梯状方式激活。我们进一步使用膜片成像表明,TRAAK和MscS的超声激活是由于膜张力增加。这些结果共同为TRAAK张力门控提供了机制性见解,为探索机械敏感钾离子通道在郎飞结中的作用提供了框架,并为将超声开发为一种用于神经调节的机械刺激技术提供了生物物理背景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0585/9882092/99d4b61e9a69/nihpp-2023.01.11.523644v1-f0001.jpg

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