Intervertebral disc human nucleus pulposus cells associated with back pain trigger neurite outgrowth in vitro and pain behaviors in rats.
Wensen JiangJuliane D GlaeserGiselle KanedaJulia SheynJacob T WechslerStephen StephanKhosrowdad SalehiJulie L ChanWafa TawackoliPablo AvalosChristopher JohnsonChloe CastanedaLinda E A KanimTeerachat TanasansomboonJoshua E BurdaOksana ShelestHaneen YameenTiffany G PerryMichael KropfJason M CuellarDror SeliktarHyun W BaeLaura S StoneDmitriy SheynPublished in: Science translational medicine (2023)
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.
Keyphrases
- endothelial cells
- chronic pain
- single cell
- induced pluripotent stem cells
- pain management
- neuropathic pain
- pluripotent stem cells
- induced apoptosis
- gene expression
- high glucose
- rna seq
- stem cells
- dna methylation
- spinal cord injury
- cell death
- mesenchymal stem cells
- drug delivery
- genome wide
- bone marrow
- endoplasmic reticulum stress
- cancer therapy