Department of Medical Genetics, Molecular and Clinical Pharmacology, Division of Biochemical Pharmacology, Medical University of Innsbruck, Peter Mayr Strasse 1, A-6020, Innsbruck, Austria.
Nat Commun. 2019 Jan 10;10(1):115. doi: 10.1038/s41467-018-07918-z.
The Ca-activated Cl channel (CaCC) TMEM16A/Anoctamin 1 (ANO1) is expressed in gastrointestinal epithelia and smooth muscle cells where it mediates secretion and intestinal motility. However, ANO1 Cl conductance has never been reported to play a role in skeletal muscle. Here we show that ANO1 is robustly expressed in the highly evolved skeletal musculature of the euteleost species zebrafish. We characterised ANO1 as bonafide CaCC which is activated close to maximum by Ca ions released from the SR during excitation-contraction (EC) coupling. Consequently, our study addressed the question about the physiological advantage of implementation of ANO1 into the euteleost skeletal-muscle EC coupling machinery. Our results reveal that Cl influx through ANO1 plays an essential role in restricting the width of skeletal-muscle action potentials (APs) by accelerating the repolarisation phase. Resulting slimmer APs enable higher AP-frequencies and apparently tighter controlled, faster and stronger muscle contractions, crucial for high speed movements.
Ca 激活的氯离子通道(CaCC)TMEM16A/ANO1(ANO1)在胃肠道上皮细胞和平滑肌细胞中表达,介导分泌和肠道蠕动。然而,ANO1 的氯离子电导从未被报道在骨骼肌中发挥作用。在这里,我们显示 ANO1 在高度进化的真骨鱼物种斑马鱼的骨骼肌中得到了强有力的表达。我们将 ANO1 鉴定为真正的 CaCC,其在兴奋-收缩(EC)偶联过程中由 SR 释放的 Ca 离子接近最大程度地激活。因此,我们的研究解决了将 ANO1 纳入真骨鱼骨骼肌 EC 偶联机制的生理优势的问题。我们的结果表明,通过 ANO1 的氯离子内流通过加速复极化阶段在限制骨骼肌动作电位(AP)的宽度方面起着至关重要的作用。由此产生的更细的 AP 能够实现更高的 AP 频率,并明显更紧密地控制更快、更强的肌肉收缩,这对于高速运动至关重要。