Zhang Tianyuan, Li Bin, Sui Wenyuan, Shao Xiexiang, Deng Yaolong, Zhang Zifang, Yang Jingfan, Huang Zifang, Li Sheng, Fu Xin, Yang Wenjun, Yang Junlin, Hu Ping
Spine Center, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Department of Spine Surgery, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
J Cell Mol Med. 2025 May;29(10):e70619. doi: 10.1111/jcmm.70619.
The aetiology of adolescent idiopathic scoliosis (AIS) is not clear, and may involve disorders in multiple systems. This study aims to perform the morphological and molecular analysis of neuromuscular junctions (NMJs) and explore the asymmetry of paraspinal muscles in AIS. We collected paraspinal muscles from AIS patients during surgery and also enrolled congenital scoliosis (CS) and non-scoliosis patients as controls. We performed immunofluorescence staining of NMJs for morphological analysis. Then, we extracted NMJs regions for further validation at the molecular level. We also explored the neurogenic abnormalities in the convex side and compared the asymmetry of paraspinal muscles. Morphological analysis of NMJs showed that the nerve terminal-related variables in the convex side were significantly decreased. The expression of denervation markers was increased in the synapse-rich regions. The expression of denervation markers in the convex paraspinal muscles was also significantly increased. Compared with CS and non-scoliosis patients, paraspinal muscles of AIS exhibited the transformation of fibre types, characterised by an increase in the proportion of type I fibres in the convex side. The phenomenon of fibre-type grouping was also noted, confirming the presence of neurogenic abnormalities. This study first investigated the morphological and molecular disorders of NMJs in the paraspinal muscles from AIS patients. We found that the neurogenic abnormalities existed in the convex side of the paraspinal muscle, which could lead to the conversion and grouping of fibre types. This resulted in an imbalance of bilateral paraspinal muscles and might be a potential driver of scoliosis.
青少年特发性脊柱侧凸(AIS)的病因尚不清楚,可能涉及多个系统的紊乱。本研究旨在对神经肌肉接头(NMJ)进行形态学和分子分析,并探讨AIS患者椎旁肌的不对称性。我们在手术过程中收集了AIS患者的椎旁肌,并纳入先天性脊柱侧凸(CS)患者和非脊柱侧凸患者作为对照。我们对NMJ进行免疫荧光染色以进行形态学分析。然后,我们提取NMJ区域以在分子水平上进行进一步验证。我们还探讨了凸侧的神经源性异常,并比较了椎旁肌的不对称性。NMJ的形态学分析表明,凸侧与神经末梢相关的变量显著减少。去神经标记物在富含突触的区域表达增加。凸侧椎旁肌中去神经标记物的表达也显著增加。与CS患者和非脊柱侧凸患者相比,AIS患者的椎旁肌表现出纤维类型的转变,其特征是凸侧I型纤维比例增加。还注意到了纤维类型分组现象,证实了神经源性异常的存在。本研究首次调查了AIS患者椎旁肌中NMJ的形态学和分子紊乱。我们发现椎旁肌凸侧存在神经源性异常,这可能导致纤维类型的转换和分组。这导致双侧椎旁肌失衡,可能是脊柱侧凸的一个潜在驱动因素。