Folia Biologica
Journal of Cellular and Molecular Biology, Charles University 

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Fol. Biol. 2026, 72, 44-53

https://doi.org/10.14712/fb2026.0004

Extraction-Dependent Immunomodulatory and Angiogenesis-Related Molecular Responses of Nigella sativa Oil in Adipose-Derived Mesenchymal Stem Cells

Badel Ince1ID, Gokturk Avsar2ID, Cagatay Han Turkseven3ID, Pelin Eroglu2ID, Gamze Ayar1ID, Murat Eser Akyurek4ID

1Department of Stem Cell and Regenerative Medicine, Institute of Health Sciences, Mersin University, Mersin, Turkey
2Department of Chemistry, Faculty of Sciences, Mersin University, Mersin, Turkey
3Department of Biophysics, Faculty of Medicine, Mersin University, Mersin, Turkey
4Atlas Biotechnology Laboratory, Ankara, Turkey

Received February 4, 2026
Accepted March 12, 2026

Nigella sativa black cumin oil (BCO) exhibits well-documented anti-inflammatory and antioxidant properties; however, the impact of extraction-related compositional variation on its cellular and molecular effects in stem cell systems remains insufficiently characterized. This study investigated the effects of cold-pressed (CP) and supercritical CO2 (ScCO2)-extracted BCO on the viability, inflammatory response and angiogenic potential of adipose-derived mesenchymal stem cells (ASCs). The oil composition and antioxidant activity were assessed using GC/MS and DPPH assays, respectively. ASCs were treated with different volumes of BCO, and cell viability was evaluated at 24, 48 and 72 h using the MTT assay. Anti-inflammatory effects were evaluated by real-time PCR analysis of IL6 and IL10 mRNA expression, while angiogenesis-related molecular responses were evaluated based on VEGF mRNA expression. Both CP and ScCO2-extracted BCO significantly increased ASC viability in a volume-dependent manner, with the highest viability consistently observed at 100 µl (P < 0.05). Treatment with 50 µl and 100 µl of either oil significantly reduced IL6 expression and concomitantly increased IL10 expression at 24 and 48 h (P < 0.05). VEGF expression was also significantly up-regulated at these time points, with ScCO2-extracted BCO inducing a more pronounced and sustained angiogenic response (P < 0.05). These findings indicate that BCO enhances ASC via­bility and molecular responses in a volume-dependent manner, while differences associated with extraction-related compositional variation may modulate inflammation- and angiogenesis-related molecular signalling in ASCs.

Funding

This study was supported by the Mersin University Scientific Research Projects Unit (Grant number 2023-1-AP4-4842).

References

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