Abstract
We evaluated the effect of morphine on human dendritic cells (DCs). Interestingly, immature DCs were found to express all 3 (μ, κ, δ) opioid receptors on the cell surface. Chronic morphine treatment (10−8 to 10−12 M) during the development of DCs from monocytes augmented LPS-induced upregulation of HLA-DR, CD86, CD80, and CD83 and increased the T cell stimulatory capacity of DCs, which could be inhibited by naloxone, an opioid receptor antagonist. The change in surface phenotype was paralleled by a p38 MAPK-dependent decrease in IL-10 and increase in IL-12 secretion. Our data indicate that morphine exerts an immunostimulatory effect by modulating LPS-induced DC maturation.
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Acknowledgments
We wish to thank Gloria Telusma and Nick Franki for their technical assistance and Cathy Rapelje for FACS analysis. We also thank Ona Bloom for critical reading of the manuscript. This work was supported by grants (5RO1DA12111) from the National Institutes of Health.
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D.M. and I.H. contributed equally to the work.
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Messmer, D., Hatsukari, I., Hitosugi, N. et al. Morphine Reciprocally Regulates IL-10 and IL-12 Production by Monocyte-Derived Human Dendritic Cells and Enhances T Cell Activation. Mol Med 12, 284–290 (2006). https://doi.org/10.2119/2006-00043.Messmer
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DOI: https://doi.org/10.2119/2006-00043.Messmer