A mechano- and heat-gated two-pore domain K + channel controls excitability in adult zebrafish skeletal muscle

Author:

Idoux Romane1,Exbrayat-Héritier Chloé2,Sohm Frédéric2,Jaque-Fernandez Francisco1ORCID,Vaganay Elisabeth2,Berthier Christine1,Bretaud Sandrine2,Jacquemond Vincent1ORCID,Ruggiero Florence2ORCID,Allard Bruno1

Affiliation:

1. 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

2. Institut de Génomique Fonctionnelle de Lyon, Ecole Normale Supérieure de Lyon, CNRS UMR 5242, Université Claude Bernard Lyon 1, Lyon 69007, France

Abstract

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 kcnk4b 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 kcnk4b 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.

Funder

Agence Nationale de la Recherche

Association Francaise contre les Myopathies

Centre National de la Recherche Scientifique

Institut National de la Santé et de la Recherche Médicale

Université Claude Bernard Lyon 1

École Normale Supérieure de Lyon

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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