Hashemolhosseini Said, Gessler Lea
Institute of Biochemistry, Medical Faculty, Friedrich-Alexander-University of Erlangen-Nürnberg, Erlangen, Germany.
Neural Regen Res. 2025 Sep 1;20(9):2464-2479. doi: 10.4103/NRR.NRR-D-24-00417. Epub 2024 Sep 6.
Skeletal muscles are essential for locomotion, posture, and metabolic regulation. To understand physiological processes, exercise adaptation, and muscle-related disorders, it is critical to understand the molecular pathways that underlie skeletal muscle function. The process of muscle contraction, orchestrated by a complex interplay of molecular events, is at the core of skeletal muscle function. Muscle contraction is initiated by an action potential and neuromuscular transmission requiring a neuromuscular junction. Within muscle fibers, calcium ions play a critical role in mediating the interaction between actin and myosin filaments that generate force. Regulation of calcium release from the sarcoplasmic reticulum plays a key role in excitation-contraction coupling. The development and growth of skeletal muscle are regulated by a network of molecular pathways collectively known as myogenesis. Myogenic regulators coordinate the differentiation of myoblasts into mature muscle fibers. Signaling pathways regulate muscle protein synthesis and hypertrophy in response to mechanical stimuli and nutrient availability. Several muscle-related diseases, including congenital myasthenic disorders, sarcopenia, muscular dystrophies, and metabolic myopathies, are underpinned by dysregulated molecular pathways in skeletal muscle. Therapeutic interventions aimed at preserving muscle mass and function, enhancing regeneration, and improving metabolic health hold promise by targeting specific molecular pathways. Other molecular signaling pathways in skeletal muscle include the canonical Wnt signaling pathway, a critical regulator of myogenesis, muscle regeneration, and metabolic function, and the Hippo signaling pathway. In recent years, more details have been uncovered about the role of these two pathways during myogenesis and in developing and adult skeletal muscle fibers, and at the neuromuscular junction. In fact, research in the last few years now suggests that these two signaling pathways are interconnected and that they jointly control physiological and pathophysiological processes in muscle fibers. In this review, we will summarize and discuss the data on these two pathways, focusing on their concerted action next to their contribution to skeletal muscle biology. However, an in-depth discussion of the non-canonical Wnt pathway, the fibro/adipogenic precursors, or the mechanosensory aspects of these pathways is not the focus of this review.
骨骼肌对于运动、姿势和代谢调节至关重要。为了理解生理过程、运动适应以及与肌肉相关的疾病,了解骨骼肌功能背后的分子途径至关重要。肌肉收缩过程由一系列复杂的分子事件相互作用协调而成,是骨骼肌功能的核心。肌肉收缩由动作电位和神经肌肉传递引发,这需要神经肌肉接头。在肌纤维内,钙离子在介导肌动蛋白和肌球蛋白丝之间产生力量的相互作用中起关键作用。肌浆网钙释放的调节在兴奋 - 收缩偶联中起关键作用。骨骼肌的发育和生长由一个统称为肌发生的分子途径网络调节。生肌调节因子协调成肌细胞向成熟肌纤维的分化。信号通路响应机械刺激和营养可用性调节肌肉蛋白质合成和肥大。包括先天性肌无力综合征、肌肉减少症、肌营养不良症和代谢性肌病在内的几种与肌肉相关的疾病,其基础是骨骼肌中分子途径失调。旨在维持肌肉质量和功能、促进再生以及改善代谢健康的治疗干预措施,通过靶向特定分子途径具有前景。骨骼肌中的其他分子信号通路包括经典Wnt信号通路,它是肌发生、肌肉再生和代谢功能的关键调节因子,以及Hippo信号通路。近年来,关于这两条途径在肌发生过程中以及在发育中和成年骨骼肌纤维中以及神经肌肉接头处的作用,已经发现了更多细节。事实上,过去几年的研究现在表明,这两条信号通路相互连接,它们共同控制肌纤维中的生理和病理生理过程。在这篇综述中,我们将总结和讨论关于这两条途径的数据,重点关注它们在对骨骼肌生物学做出贡献之外的协同作用。然而,对非经典Wnt途径、成纤维/脂肪生成前体或这些途径的机械感觉方面的深入讨论不是本综述的重点。