Pomella Silvia, Cassandri Matteo, Antoniani Francesco, Crotti Samuele, Mediani Laura, Silvestri Beatrice, Medici Margherita, Rota Rossella, Rosa Alessandro, Carra Serena
Department of Oncohematology, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.
Muscles. 2023 Apr 18;2(2):187-203. doi: 10.3390/muscles2020014.
The skeletal muscle is a highly plastic tissue that shows a remarkable adaptive capacity in response to acute and resistance exercise, and modifies its composition to adapt to use and disuse, a process referred to as muscle plasticity. Heat shock proteins (HSPs), a class of evolutionarily conserved molecular chaperones, have been implicated in the regulation of skeletal muscle plasticity. Here, we summarize key findings supporting the notion that HSPs are important components required to maintain skeletal muscle integrity and functionality. HSPs participate in the transcriptional program required for myogenesis and are activated following muscle exercise and injury. Their dysfunction, either as a consequence of improper expression or genetic mutations, contributes to muscle atrophy and leads to the development of myopathies and peripheral motor neuropathies. Denervation/reinnervation and repeated rounds of nerve degeneration/regeneration have been observed in motor neuropathies, suggesting that an imbalance in HSP expression and function may impair the repair of the neuromuscular junctions. Boosting HSP activity may help preventing muscle atrophy by promoting muscle differentiation and helping the repair of NMJs. Boosting HSP function may also help to combat the development of rhabdomyosarcoma (RMS), a highly aggressive type of pediatric soft tissue sarcoma whose cells have skeletal muscle features but are unable to fully differentiate into skeletal muscle cells.
骨骼肌是一种高度可塑性的组织,在急性运动和抗阻运动时表现出显著的适应能力,并改变其组成以适应使用和废用情况,这一过程称为肌肉可塑性。热休克蛋白(HSPs)是一类进化上保守的分子伴侣,参与骨骼肌可塑性的调节。在此,我们总结了关键研究结果,支持HSPs是维持骨骼肌完整性和功能所必需的重要组成部分这一观点。HSPs参与肌生成所需的转录程序,并在肌肉运动和损伤后被激活。它们的功能障碍,无论是由于表达不当还是基因突变,都会导致肌肉萎缩,并引发肌病和周围运动神经病。在运动神经病中观察到去神经支配/再支配以及反复的神经变性/再生,这表明HSPs表达和功能的失衡可能会损害神经肌肉接头的修复。提高HSPs活性可能有助于通过促进肌肉分化和帮助神经肌肉接头的修复来预防肌肉萎缩。提高HSPs功能也可能有助于对抗横纹肌肉瘤(RMS)的发展,RMS是一种侵袭性很强的儿童软组织肉瘤,其细胞具有骨骼肌特征,但无法完全分化为骨骼肌细胞。