Intervertebral disc human nucleus pulposus cells associated with back pain trigger neurite outgrowth in vitro and pain behaviors in rats

椎间盘 神经突 体外 医学 核心 腰痛 伤害感受器 病理 神经科学 细胞生物学 解剖 伤害 生物 内科学 受体 替代医学 生物化学
作者
Wensen Jiang,Juliane D. Glaeser,Giselle Kaneda,Julia Sheyn,Jacob T. Wechsler,Stephen Stephan,Khosrowdad Salehi,Julie L. Chan,Wafa Tawackoli,Pablo Avalos,Christopher N. Johnson,Chloe Castaneda,Linda E.A. Kanim,Teerachat Tanasansomboon,Joshua E. Burda,Oksana Shelest,Haneen Simaan Yameen,Tiffany G. Perry,Michael A. Kropf,Jason M. Cuéllar
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science]
卷期号:15 (725) 被引量:20
标识
DOI:10.1126/scitranslmed.adg7020
摘要

Low back pain (LBP) is often associated with the degeneration of human intervertebral discs (IVDs). However, the pain-inducing mechanism in degenerating discs remains to be elucidated. Here, we identified a subtype of locally residing human nucleus pulposus cells (NPCs), generated by certain conditions in degenerating discs, that was associated with the onset of discogenic back pain. Single-cell transcriptomic analysis of human tissues showed a strong correlation between a specific cell subtype and the pain condition associated with the human degenerated disc, suggesting that they are pain-triggering. The application of IVD degeneration-associated exogenous stimuli to healthy NPCs in vitro recreated a pain-associated phenotype. These stimulated NPCs activated functional human iPSC-derived sensory neuron responses in an in vitro organ-chip model. Injection of stimulated NPCs into the healthy rat IVD induced local inflammatory responses and increased cold sensitivity and mechanical hypersensitivity. Our findings reveal a previously uncharacterized pain-inducing mechanism mediated by NPCs in degenerating IVDs. These findings could aid in the development of NPC-targeted therapeutic strategies for the clinically unmet need to attenuate discogenic LBP.
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