Page 62 - M. Immunology
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[M. Immunology-37]



                   Inotodiol, a novel lanostane triterpenoid from Chaga


                    mushroom Inonotus Obliquus induces characteristic


                                      maturation of dendritic cells



           Perry Ayn Mayson A. Maza¹˙², Ji-Hyeon Lee¹˙², Min-Sook Ryu³, Ludmila P. Ponomarenko⁴, Valentin A. Stonik⁴,

                                                 Jong-Young Kwak¹˙²˙³˙*


         ¹Department of Pharmacology, School of Medicine, Ajou University , Suwon  16499, South Korea, ²Department of

         Biomedical Sciences, Graduate school, Ajou University, Suwon  16499, South Korea, ³Department of Allergy, Ajou
          University School of Medicine, Suwon  16499, South Korea, ⁴Department of Bioorganic Chemistry, Far Eastern
                         Branch of the Russian Academy of Sciences, Russian Federation 690022, Russia





        Dendritic cells(DCs) have the ability to stimulate naïve T cells that coordinate subsequent adaptive response towards
        inflammatory response or tolerance depending on the DC differentiation level. Inotodiol, a lanostane triterpenoid

        from Inonotus obliquus (wild Chaga mushroom) is as a natural compound. In this study, we investigated whether
        inotodiol  promotes  maturation  of  bone-marrow-derived  DC(BMDC)  and  induces  T  cell  proliferation.  Inotodiol

        increased the expression of surface maturation markers, including MHC-II, CD86, and CD40 on BMDCs with almost
        no production of various cytokines, including TNF-α and IL-12p40 from the BMDCs. OT-I T cells primed by OVA-

        pulsed inotodiol-treated BMDCs proliferated and produced IL-2 with other cytokines, including IL-12p40 and INF-
        γ. Specific inhibitor of PI3K abrogated the effects of inotodiol on upregulation of CD86 and MHC-II, whereas inhibitor

        of NF-κB inhibited their expression both by LPS an inotodiol. SB216763, specific inhibitor of GSK-3β alone up-
        regulated CD86 expression and augmented the upregulation of CD86 expression by inotodiol in BMDCs. These
        results  suggest  that  inotodiol  induces  DCs  a  characteristic  type  of  maturation  through  PI3K  activation  in

        independence of NF-κB and inotodiol-treated DCs enhance T cell production of IL-2.
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