Department of Molecular & Cell Biology, University of California Berkeley, Berkeley, CA, 94720, USA.
Helen Wills Neuroscience Institute, University of California Berkeley, Berkeley, CA, 94720, USA.
Nat Commun. 2024 Apr 11;15(1):3142. doi: 10.1038/s41467-024-47208-5.
TRAAK, TREK-1, and TREK-2 are mechanosensitive two-pore domain K+ (K2P) channels that contribute to action potential propagation, sensory transduction, and muscle contraction. While structural and functional studies have led to models that explain their mechanosensitivity, we lack a quantitative understanding of channel activation by membrane tension. Here, we define the tension response of mechanosensitive K2Ps using patch-clamp recording and imaging. All are low-threshold mechanosensitive channels (T 0.6-2.7 / 4.4-6.4 mN/m) with distinct response profiles. TRAAK is most sensitive, TREK-1 intermediate, and TREK-2 least sensitive. TRAAK and TREK-1 are activated broadly over a range encompassing nearly all physiologically relevant tensions. TREK-2, in contrast, activates over a narrower range like mechanosensitive channels Piezo1, MscS, and MscL. We further show that low-frequency, low-intensity focused ultrasound increases membrane tension to activate TRAAK and MscS. This work provides insight into tension gating of mechanosensitive K2Ps relevant to understanding their physiological roles and potential applications for ultrasonic neuromodulation.
TRAAK、TREK-1 和 TREK-2 是机械敏感的双孔域钾离子(K2P)通道,它们有助于动作电位的传播、感觉转导和肌肉收缩。虽然结构和功能研究已经提出了解释其机械敏感性的模型,但我们缺乏对膜张力激活通道的定量理解。在这里,我们使用膜片钳记录和成像来定义机械敏感 K2P 的张力反应。所有这些都是低阈值机械敏感通道(T 0.6-2.7/4.4-6.4 mN/m),具有不同的反应特征。TRAAK 最敏感,TREK-1 中等,TREK-2 最不敏感。TRAAK 和 TREK-1 在几乎所有生理相关张力范围内广泛激活。相比之下,TREK-2 的激活范围较窄,类似于机械敏感通道 Piezo1、MscS 和 MscL。我们还表明,低频、低强度聚焦超声会增加膜张力以激活 TRAAK 和 MscS。这项工作深入了解了机械敏感 K2P 的张力门控,这对于理解它们的生理作用以及超声神经调节的潜在应用具有重要意义。