Department of Pharmacology, School of Medicine, Ajou University, Suwon, South Korea.
Department of Biomedical Sciences, The Graduate School, Ajou University, Suwon, South Korea.
Front Immunol. 2021 Mar 12;12:650841. doi: 10.3389/fimmu.2021.650841. eCollection 2021.
Dendritic cells (DCs) have the ability to stimulate naïve T cells that coordinate subsequent adaptive response toward an inflammatory response or tolerance depending on the DC differentiation level. Inotodiol, a lanostane triterpenoid found in (wild Chaga mushroom), is a natural compound with a wide range of biological activities. In this study, we investigated whether inotodiol promotes the maturation of bone marrow-derived DCs (BMDCs) and inotodiol-treated BMDCs induce T cell activation. Inotodiol increased the expression of surface maturation markers, including MHC-I, MHC-II, CD86, and CD40, on BMDCs without affecting the production of various cytokines, including TNF-α and IL-12p40 in these cells. T cells primed with inotodiol-treated BMDCs proliferated and produced IL-2, without producing other cytokines, including IL-12p40 and IFN-γ. Injection of inotodiol into mice induced maturation of splenic DCs and IL-2 production, and the administration of inotodiol and inotodiol-treated BMDCs induced the proliferation of adoptively transferred CD8 T cells . The phosphatidylinositol-3-kinase inhibitor wortmannin abrogated the upregulation of Akt phosphorylation and CD86 and MHC-II expression induced by inotodiol. However, inotodiol failed to induce phosphorylation of the IκB kinase and degradation of IκB-α, and increased expression of CD86 induced by inotodiol was not blocked by an IκB kinase inhibitor. These results suggest that inotodiol induces a characteristic type of maturation in DCs through phosphatidylinositol-3-kinase activation independent of NF-κB, and inotodiol-treated DCs enhance T cell proliferation and IL-2 secretion.
树突状细胞(DCs)具有刺激初始 T 细胞的能力,根据 DC 分化水平的不同,这种刺激可协调随后的炎症反应或耐受反应。来源于(野生桦褐孔菌)的羊毛甾烷三萜类化合物——桦褐孔菌醇,是一种具有广泛生物活性的天然化合物。在本研究中,我们研究了桦褐孔菌醇是否能促进骨髓来源的树突状细胞(BMDCs)的成熟,以及桦褐孔菌醇处理的 BMDCs 是否能诱导 T 细胞活化。桦褐孔菌醇增加了 BMDCs 表面成熟标志物的表达,包括 MHC-I、MHC-II、CD86 和 CD40,而不影响这些细胞中各种细胞因子(包括 TNF-α 和 IL-12p40)的产生。用桦褐孔菌醇处理的 BMDCs 激活的 T 细胞增殖并产生 IL-2,而不产生其他细胞因子,包括 IL-12p40 和 IFN-γ。向小鼠体内注射桦褐孔菌醇诱导脾 DCs 的成熟和 IL-2 的产生,而给予桦褐孔菌醇和桦褐孔菌醇处理的 BMDCs 则诱导过继转移的 CD8 T 细胞的增殖。磷脂酰肌醇-3-激酶抑制剂wortmannin 阻断了桦褐孔菌醇诱导的 Akt 磷酸化和 CD86、MHC-II 表达的上调。然而,桦褐孔菌醇不能诱导 IκB 激酶的磷酸化和 IκB-α的降解,并且桦褐孔菌醇诱导的 CD86 表达增加不受 IκB 激酶抑制剂的阻断。这些结果表明,桦褐孔菌醇通过独立于 NF-κB 的磷脂酰肌醇-3-激酶的激活诱导 DC 产生一种特征性的成熟类型,桦褐孔菌醇处理的 DCs 增强了 T 细胞的增殖和 IL-2 的分泌。