ArticleJOR spine2025
Understanding the Physiological Behavior of Disc Cells in an In Vitro Imitation of the Healthy and Degenerated Disc Niche.
Article in JOR spine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- MnOMaterials today. Bio · 2026Article
- Defining the Human Nucleus Pulposus Microenvironment and Its Impact on Cell Matrix Synthesis and Metabolic Activity.JOR spine · 2026Article
- Understanding the Physiological Behavior of Disc Cells in an In Vitro Imitation of the Healthy and Degenerated Disc Niche.JOR spine · 2025Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: The natural environment within the nucleus pulposus (NP) is hypoxic, acidic, low in nutrition, and exerts a high osmotic pressure. NP cells have adapted to this harsh environment; however, in vitro conditions often fail to recapitulate this environment. Hence, this study aimed to develop media to mimic the conditions of the native NP, with regards to pH, osmolality, glucose, combined with culture in physioxia (5% O Methods: All media utilized low glucose DMEM/serum free conditions with supplements supporting matrix synthesis, based on media recommended for alginate culture (standard media). Healthy media modulated osmolarity (425 mOsm/kg) and pH 7.2; degenerate media consisted of 325 mOsm/kg and pH 6.8. The latter was further supplemented with 100 pg/mL IL-1β (degenerate+IL-1β media). NP cells in 3D alginate and NP tissue explants were cultured in these media for up to 2 weeks in physioxia (5% O Results: Media osmolarity and pH remained stable and cell viability was not altered by any media composition. Mitochondrial activity was increased during short-term cultures, whilst a decrease was seen following 14 days in degenerate media. The secretome of NP cells was differentially affected in healthy or degenerate media, with most increases in catabolic cytokines observed following the addition of IL-1β. Tissue explants showed stability of protein expression of matrix components in both healthy and degenerate+IL-1β media, with limited effects seen on the secretome. Discussion: The media formulations developed here can provide more appropriate environmental conditions in vitro, mimicking more closely the in vivo conditions observed within healthy and degenerate IVDs. The application of which can provide more appropriate culture conditions to test potential therapeutic approaches and understand more fully the pathogenesis of disease using in vitro and ex vivo models.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.