Physiopathologie et Génétique du Neurone et du Muscle, Université Claude Bernard Lyon 1, CNRS UMR 5261, INSERM U1315, Faculté de Médecine Rockefeller, Lyon 69008, France.
Institut de Génomique Fonctionnelle de Lyon, Ecole Normale Supérieure de Lyon, CNRS UMR 5242, Université Claude Bernard Lyon 1, Lyon 69007, France.
Proc Natl Acad Sci U S A. 2023 Nov 7;120(45):e2305959120. doi: 10.1073/pnas.2305959120. Epub 2023 Oct 30.
TRAAK channels are mechano-gated two-pore-domain K channels. Up to now, activity of these channels has been reported in neurons but not in skeletal muscle, yet an archetype of tissue challenged by mechanical stress. Using patch clamp methods on isolated skeletal muscle fibers from adult zebrafish, we show here that single channels sharing properties of TRAAK channels, i.e., selective to K ions, of 56 pS unitary conductance in the presence of 5 mM external K, activated by membrane stretch, heat, arachidonic acid, and internal alkaline pH, are present in enzymatically isolated fast skeletal muscle fibers from adult zebrafish. The transcript encoding for TRAAK channels was cloned and found, concomitantly with activity of mechano-gated K channels, to be absent in zebrafish fast skeletal muscles at the larval stage but arising around 1 mo of age. The transfer of the gene in HEK cells and in the adult mouse muscle, that do not express functional TRAAK channels, led to expression and activity of mechano-gated K channels displaying properties comparable to native zebrafish TRAAK channels. In whole-cell voltage-clamp and current-clamp conditions, membrane stretch and heat led to activation of macroscopic K currents and to acceleration of the repolarization phase of action potentials respectively, suggesting that heat production and membrane deformation associated with skeletal muscle activity can control muscle excitability through TRAAK channel activation. TRAAK channels may represent a teleost-specific evolutionary product contributing to improve swimming performance for escaping predators and capturing prey at a critical stage of development.
TRAAK 通道是机械门控双孔域 K 通道。到目前为止,这些通道的活性已在神经元中报道,但不在骨骼肌中,而骨骼肌是受机械应激挑战的组织原型。我们使用成年斑马鱼分离的骨骼肌纤维的膜片钳方法,在此显示在成年斑马鱼的酶分离的快肌纤维中存在具有 TRAAK 通道特性的单个通道,即选择性对 K 离子,在 5 mM 外部 K 存在时具有 56 pS 的单位电导,由膜拉伸、热、花生四烯酸和内部碱性 pH 激活。编码 TRAAK 通道的 转录本被克隆,并与机械门控 K 通道的活性同时发现,在斑马鱼幼虫阶段不存在于快肌中,但在 1 个月左右的年龄出现。将 基因转染到 HEK 细胞和成年小鼠肌肉中,这些细胞不表达功能性 TRAAK 通道,导致表达和活性的机械门控 K 通道显示出与天然斑马鱼 TRAAK 通道相当的特性。在全细胞膜电压钳和电流钳条件下,膜拉伸和热分别导致宏观 K 电流的激活和动作电位复极化阶段的加速,表明与骨骼肌活动相关的热产生和膜变形可以通过 TRAAK 通道激活来控制肌肉兴奋性。TRAAK 通道可能代表一种硬骨鱼特有的进化产物,有助于在发育的关键阶段提高游泳性能,以逃避捕食者和捕捉猎物。