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单细胞转录组分析揭示生物力学负荷诱导的骨与脂肪失衡,导致腰椎间盘髓核退变中的骨化。

Single-Cell Transcriptomic Analysis Reveals Biomechanical Loading-Induced Imbalance in Bone and Fat, Leading to Ossification in Lumbar Intervertebral Disc Nucleus Pulposus Degeneration.

作者信息

Zhang Ping, Wang Yuan, Bai Jianqi, Zhang Jingru, Zhang Shimin, Guo Xiaofei, Zhan Jiawen, Zhu Liguo

机构信息

Department of Pathology, Wangjing Hospital of China Academy of Chinese Medical Sciences, Beijing, China.

Department of Spine, Wangjing Hospital of China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

J Cell Physiol. 2025 Jan;240(1):e31506. doi: 10.1002/jcp.31506.

Abstract

In this study, we explored the impact of different biomechanical loadings on lumbar spine motion segments, particularly concerning intervertebral disc degeneration (IVDD). We aimed to uncover the cellular milieu and mechanisms driving ossification in the nucleus pulposus (NP) during IVDD, a process whose underlying mechanisms have remained elusive. The study involved the examination of fresh NP tissue from the L3-S1 segment of five individuals, either with IVDD or healthy. The analysis consisted of histopathological evaluation and single-cell RNA sequencing. To further validate the impact of biomechanical loading on IVDD, particularly on the CITED4 + METRN + NP chondrocytes and the bone-fat balance mechanism, a retrospective analysis was conducted using paraffin-embedded NP samples from patients. A distinct subset of CITED4 + METRN+ chondrocytes in the degenerated NP that were influenced by biomechanical loading was identified. These cells were evaluated for their potential as diagnostic biomarkers. Pseudotemporal analysis indicated that inflammation and repair processes were integral to NP ossification. Notably, the L4/5 and L5/S1 segments with severe IVDD showed pronounced ossification and heightened lipogenic metabolism. Cell communication analysis sheds light on the roles of bone-fat balance proteins and various ossification genes. Additionally, immunohistochemistry and immunofluorescence confirmed that biomechanical loading intensified IVDD by fostering osteogenic differentiation, mediated by macrophage migration inhibitory factor (MIF)-regulated bone-fat balance. This research reveals the microenvironmental factors of IVDD NP ossification under biomechanical loading, highlighting the role of bone-fat imbalance. These insights significantly enhance the understanding of IVDD pathogenesis and pave the way for innovative therapeutic approaches.

摘要

在本研究中,我们探讨了不同生物力学负荷对腰椎运动节段的影响,特别是关于椎间盘退变(IVDD)。我们旨在揭示IVDD过程中髓核(NP)骨化的细胞环境和驱动机制,这一过程的潜在机制一直难以捉摸。该研究涉及检查来自五名个体L3 - S1节段的新鲜NP组织,这些个体要么患有IVDD,要么健康。分析包括组织病理学评估和单细胞RNA测序。为了进一步验证生物力学负荷对IVDD的影响,特别是对CITED4 + METRN + NP软骨细胞和骨 - 脂肪平衡机制的影响,我们使用患者的石蜡包埋NP样本进行了回顾性分析。在退变的NP中鉴定出受生物力学负荷影响的CITED4 + METRN +软骨细胞的一个独特亚群。对这些细胞作为诊断生物标志物的潜力进行了评估。伪时间分析表明炎症和修复过程是NP骨化所必需的。值得注意的是,患有严重IVDD的L4/5和L5/S1节段显示出明显的骨化和增强的脂肪生成代谢。细胞通讯分析揭示了骨 - 脂肪平衡蛋白和各种骨化基因的作用。此外,免疫组织化学和免疫荧光证实,生物力学负荷通过促进成骨分化加剧了IVDD,这是由巨噬细胞迁移抑制因子(MIF)调节的骨 - 脂肪平衡介导的。这项研究揭示了生物力学负荷下IVDD NP骨化的微环境因素,突出了骨 - 脂肪失衡的作用。这些见解显著增强了对IVDD发病机制的理解,并为创新治疗方法铺平了道路。

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