Dufresne Sébastien S, Dumont Nicolas A, Boulanger-Piette Antoine, Fajardo Val A, Gamu Daniel, Kake-Guena Sandrine-Aurélie, David Rares Ovidiu, Bouchard Patrice, Lavergne Éliane, Penninger Josef M, Pape Paul C, Tupling A Russell, Frenette Jérôme
Centre Hospitalier Universitaire de Québec-Centre de Recherche du Centre Hospitalier de l'Université Laval, Université Laval, Quebec City, Quebec, Canada;
Department of Kinesiology, University of Waterloo, Waterloo, Ontario, Canada;
Am J Physiol Cell Physiol. 2016 Apr 15;310(8):C663-72. doi: 10.1152/ajpcell.00285.2015. Epub 2016 Jan 28.
Receptor-activator of nuclear factor-κB (RANK), its ligand RANKL, and the soluble decoy receptor osteoprotegerin are the key regulators of osteoclast differentiation and bone remodeling. Here we show that RANK is also expressed in fully differentiated myotubes and skeletal muscle. Muscle RANK deletion has inotropic effects in denervated, but not in sham, extensor digitorum longus (EDL) muscles preventing the loss of maximum specific force while promoting muscle atrophy, fatigability, and increased proportion of fast-twitch fibers. In denervated EDL muscles, RANK deletion markedly increased stromal interaction molecule 1 content, a Ca(2+)sensor, and altered activity of the sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA) modulating Ca(2+)storage. Muscle RANK deletion had no significant effects on the sham or denervated slow-twitch soleus muscles. These data identify a novel role for RANK as a key regulator of Ca(2+)storage and SERCA activity, ultimately affecting denervated skeletal muscle function.
核因子κB受体激活剂(RANK)、其配体RANKL以及可溶性诱饵受体骨保护素是破骨细胞分化和骨重塑的关键调节因子。在此我们表明,RANK也在完全分化的肌管和骨骼肌中表达。肌肉中RANK缺失对去神经支配的趾长伸肌(EDL)有正性肌力作用,但对假手术组的EDL肌肉无此作用,可防止最大比肌力的丧失,同时促进肌肉萎缩、疲劳,并增加快肌纤维比例。在去神经支配的EDL肌肉中,RANK缺失显著增加了基质相互作用分子1的含量(一种Ca²⁺传感器),并改变了肌浆网Ca²⁺-ATP酶(SERCA)调节Ca²⁺储存的活性。肌肉中RANK缺失对假手术组或去神经支配的慢肌比目鱼肌无显著影响。这些数据确定了RANK作为Ca²⁺储存和SERCA活性的关键调节因子的新作用,最终影响去神经支配的骨骼肌功能。