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单细胞转录组分析揭示了骨化后纵韧带中I型干扰素信号通路的激活。

Single-cell transcriptome profiling identifies the activation of type I interferon signaling in ossified posterior longitudinal ligament.

作者信息

Liu Xiao, Zhang Lei, Wang Ge, Zhao Wei, Liang Chen, Tang Youzhi, Fu Yenan, Liu Bo, Zhang Jing, Liu Xiaoguang, Zhang Hongquan, Yu Yu

机构信息

Department of Orthopedics and Beijing Key Laboratory of Spinal Disease Research, Peking University Third Hospital, Beijing, 100191, China.

Department of Human Anatomy, Histology and Embryology, School of Basic Medical Sciences, State Key Laboratory of Molecular Oncology and International Cancer Institute, Peking University Health Science Center, Beijing, 100191, China.

出版信息

Front Med. 2024 Dec;18(6):1087-1099. doi: 10.1007/s11684-024-1075-5. Epub 2024 Oct 23.

Abstract

Ossification of the posterior longitudinal ligament (OPLL) is a condition comprising ectopic bone formation from spinal ligaments. This disease is a leading cause of myelopathy in the Asian population. However, the molecular mechanism underlying OPLL and efficient preventive interventions remain unclear. Here, we performed single-cell RNA sequencing and revealed that type I interferon (IFN) signaling was activated in the ossified ligament of patients with OPLL. We also observed that IFN-β stimulation promoted the osteogenic differentiation of preosteoblasts in vitro and activated the ossification-related gene SPP1, thereby confirming the single-cell RNA sequencing findings. Further, blocking the IFN-α/β subunit 1 receptor (IFNAR1) using an anti-IFNAR1 neutralizing antibody markedly suppressed osteogenic differentiation. Together, these results demonstrated that the type I IFN signaling pathway facilitated ligament ossification, and the blockade of this signaling might provide a foundation for the prevention of OPLL.

摘要

后纵韧带骨化(OPLL)是一种由脊柱韧带异位骨化形成的病症。这种疾病是亚洲人群脊髓病的主要病因。然而,OPLL的分子机制和有效的预防干预措施仍不清楚。在此,我们进行了单细胞RNA测序,并揭示I型干扰素(IFN)信号在OPLL患者的骨化韧带中被激活。我们还观察到IFN-β刺激在体外促进了前成骨细胞的成骨分化,并激活了与骨化相关的基因SPP1,从而证实了单细胞RNA测序的结果。此外,使用抗IFNAR1中和抗体阻断IFN-α/β亚基1受体(IFNAR1)可显著抑制成骨分化。总之,这些结果表明I型IFN信号通路促进了韧带骨化,阻断该信号可能为预防OPLL提供基础。

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