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Updated: Mar 31, 2026

A Proinflammatory, Degenerative Organ Culture Model to Simulate Early-Stage Intervertebral Disc Disease.
Published on: February 14, 2021
Intervertebral Disc Cells Produce Interleukins Found in Patients with Back Pain
Yejia Zhang1, Ana Chee, Peng Shi
1From the Departments of Physical Medicine & Rehabilitation (YZ, CTP) and Orthopedic Surgery (YZ, HES), Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Translational Musculoskeletal Research Center (TMRC), Philadelphia Veterans Affairs Medical Center, Philadelphia, Pennsylvania (YZ, HES); Department of Orthopedic Surgery, Rush University Medical Center, Chicago, Illinois (AC, PS, HSA); Department of Biochemistry, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania (SLA); Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois (YD); and Department of Orthopedic Surgery, Thomas Jefferson University, Philadelphia, Pennsylvania (DZM, DGA).
Insights
Intervertebral disc (IVD) cells produce inflammatory cytokines like IL-8, IL-7, and IL-10. Elevated levels of these cytokines in annulus fibrosus (AF) tissues correlate with axial back pain, suggesting their role in discogenic pain.
Area of Science:
- Biomedical Science
- Molecular Biology
- Immunology
Background:
- Axial back pain is a prevalent condition with complex etiologies.
- Intervertebral disc (IVD) degeneration is implicated in back pain, but the specific molecular mechanisms remain incompletely understood.
- Cytokines, signaling proteins involved in inflammation, are potential contributors to pain signaling within the IVD.
Purpose of the Study:
- To investigate the relationship between specific cytokines within human intervertebral disc (IVD) tissues and the presence of axial back pain.
- To determine if IVD cells cultured in vitro produce inflammatory cytokines in response to stimulation.
- To compare cytokine expression profiles in annulus fibrosus (AF) tissues from patients with and without back pain.
Main Methods:
- Human IVD cells (nucleus pulposus and annulus fibrosus) were cultured and stimulated with interleukin (IL)-1β.
- Gene expression of IL-8 and IL-7 was quantified using real-time polymerase chain reaction.
- Protein levels of IL-8 were measured by enzyme-linked immunosorbent assay.
- Cytokine profiles in AF tissues from back pain patients and controls were analyzed using cytokine arrays.
Main Results:
- IL-1β stimulation significantly upregulated IL-8 gene and protein expression in both nucleus pulposus (NP) and AF cells.
- IL-7 gene expression also increased in NP cells following IL-1β stimulation.
- AF tissues from patients with back pain exhibited significantly higher levels of IL-8, IL-7, and IL-10 compared to control tissues.
Conclusions:
- IVD cells, specifically NP and AF cells, are capable of producing key inflammatory cytokines.
- Elevated levels of IL-8, IL-7, and IL-10 in AF tissues are associated with discogenic back pain.
- These findings suggest that inflammatory mediators produced by IVD cells play a significant role in the pathophysiology of axial back pain.
Objective:
To examine the link between cytokines in intervertebral disc (IVD) tissues and axial back pain.
Design:
In vitro study with human IVD cells cultured from cadaveric donors and annulus fibrosus (AF) tissues from patients.
Results:
Cultured nucleus pulposus (NP) and AF cells were stimulated with interleukin (IL)-1β. IL-8 and IL-7 gene expression was analyzed using real-time polymerase chain reaction. IL-8 protein was quantified by enzyme-linked immunosorbent assay. After IL-1β stimulation, IL-8 gene expression increased 26,541 fold in NP cells and 22,429 fold in AF cells, whereas protein released by the NP and AF cells increased 2,389- and 1,784-fold, respectively. IL-7 gene expression increased 3.3-fold in NP cells (P < 0.05).Cytokine profiles in AF tissues collected from patients undergoing surgery for back pain (painful group) or scoliosis (controls) were compared by cytokine array. IL-8 protein in the AF tissues from patients with back pain was 1.81-fold of that in controls. IL-7 and IL-10 in AF tissues from the painful group were 6.87 and 4.63 times greater than the corresponding values in controls, respectively (P < 0.05).
Conclusion:
Inflammatory mediators found in AF tissues from patients with discogenic back pain are likely produced by IVD cells and may play a key role in back pain.
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