Sesamolin affects both natural killer cells and cancer cells in order to create an optimal environment for cancer cell sensitization.

Abstract

In our previous study, we demonstrated that sesamolin can increase the level of cancer cell susceptibility to natural killer (NK) cell mediated cytolysis when it treats cancer cells. The present study attempted to demonstrate the direct influence of sesamolin on NK cells. To achieve the study goal, an NK cell (NK-92MI) or Raji cell was treated with sesamolin for use in the analysis of the cytolytic activity of NK cells. When NK-92MI cells were treated with sesamolin, the cytolysis activities of NK cells increased depending on the concentration of sesamolin. However, the highest cytolytic activity of NK cells was observed when Raji and NK-92MI cells were treated with sesamolin at 20 μg/mL and 40 μg/mL, respectively. Sesamolin also increased the expression of the degranulation marker, CD107a, on the surface of NK cells and the production of immune-activation cytokine, IFN-γ, from NK cells. The effects of sesamolin on NK cells were reproduced in the naïve NK cells. We found that sesamolin effects are triggered by the result of phosphorylation of the p38, ERK1/2 and JNK pathways in NK cells. Taken together, this study proved that NK cell activity can be increased by the stimulation of sesamolin on NK cells as well as cancer cells.

• Authors: Seo Eun Lee, Jae Kwon Lee
• Journal: International immunopharmacology (Int Immunopharmacol) Vol. 64 Pg. 16-23 (Nov 2018) ISSN: 1878-1705 [Electronic] Netherlands
• PMID: 30144640 (Publication Type: Journal Article)
• Copyright: Copyright © 2018 Elsevier B.V. All rights reserved.

Chemical References

• Dioxoles
• KLRK1 protein, human
• Lysosomal-Associated Membrane Protein 1
• NK Cell Lectin-Like Receptor Subfamily K
• sesamolin

Topics

• Cell Line, Tumor
• Cell Survival (drug effects)
• Cytotoxicity, Immunologic (drug effects)
• Dioxoles (pharmacology)
• Humans
• Killer Cells, Natural (drug effects, immunology)
• Lymphocyte Activation (drug effects)
• Lysosomal-Associated Membrane Protein 1 (analysis)
• NK Cell Lectin-Like Receptor Subfamily K (analysis)
• Neoplasms (drug therapy, immunology)