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Cannabidiol modulates classical and non-classical HLA expression in human choriocarcinoma cell line
Kevin I Martínez1, María B Palma2, Fernando J Sepúlveda3
1Department of Citology, Histology and Embriology, School of Medical Sciences, National University of La Plata, La Plata, Argentina; National Scientific and Technical Research Council (CONICET), Argentina.
Abstract:
Cannabidiol (CBD) modulates diverse signaling pathways with potential relevance to tumor immune escape; however, its impact on the regulation of classical and non-classical HLA class I molecules remains incompletely understood. Here, we examined the effects of CBD on HLA expression in JEG-3 choriocarcinoma cells, focusing on cannabinoid-related receptors and intracellular Ca2+ signaling. CBD increased the expression of classical HLA class I genes, most notably HLA-C, while reducing HLA-G levels, a non-classical HLA class I molecule associated with local immunosuppressive functions. Receptor profiling revealed constitutive expression of CB1 and CB2, whereas GPR55 and PPARγ expression became detectable only after CBD exposure. Receptor inhibition assays showed that HLA-G downregulation was selectively attenuated by CB1 blockade, with no meaningful contribution from CB2 or GPR55. In contrast, CBD-induced HLA-C upregulation was significantly attenuated by GPR55 and CB2 inhibition, while remaining unaffected by CB1 blockade, suggesting distinct receptor-associated pathways for classical and non-classical HLA regulation. Calcium chelation using BAPTA further demonstrated that HLA-G modulation was highly sensitive to intracellular Ca2+ reduction, whereas classical HLA expression required higher BAPTA concentrations to be affected. Altogether, these findings support the possibility that CBD may promote coordinated immunomodulatory effects associated with differential regulation of classical and non-classical HLA molecules through receptor-associated and calcium-sensitive signaling pathways.
Insights
Cannabidiol (CBD) differentially regulates HLA class I molecules in choriocarcinoma cells. CBD impacts tumor immune escape by modulating HLA-C and HLA-G expression via specific receptors and calcium signaling.
Area of Science:
- Immunology
- Molecular Biology
- Pharmacology
Background:
- Cannabidiol (CBD) is known to modulate signaling pathways relevant to tumor immune escape.
- The precise effects of CBD on Human Leukocyte Antigen (HLA) class I molecule regulation, crucial for immune response, are not fully understood.
Purpose of the Study:
- To investigate the impact of CBD on the expression of classical (e.g., HLA-C) and non-classical (e.g., HLA-G) HLA class I molecules.
- To explore the roles of cannabinoid receptors (CB1, CB2), G protein-coupled receptor 55 (GPR55), peroxisome proliferator-activated receptor gamma (PPARγ), and intracellular calcium (Ca2+) signaling in CBD's effects.
Main Methods:
- Treatment of JEG-3 choriocarcinoma cells with CBD.
- Analysis of HLA class I gene expression.
- Receptor profiling and inhibition assays using specific antagonists.
- Intracellular calcium modulation using BAPTA.
Main Results:
- CBD increased classical HLA class I (notably HLA-C) and decreased non-classical HLA-G expression.
- CBD induced expression of GPR55 and PPARγ.
- HLA-G downregulation was mediated by CB1, while HLA-C upregulation involved GPR55 and CB2.
- HLA-G regulation was sensitive to reduced intracellular Ca2+, whereas classical HLA expression required more significant Ca2+ reduction.
Conclusions:
- CBD exerts immunomodulatory effects by differentially regulating classical and non-classical HLA class I molecules.
- These effects are mediated through distinct receptor-associated and calcium-sensitive signaling pathways.
- CBD's action on HLA expression suggests a potential role in modulating tumor immune escape mechanisms.

