Sinulariolide suppresses LPS-induced phenotypic and functional maturation of dendritic cells
Author(s) -
Ting-Wen Chung,
YiRong Li,
Wei Huang,
JuiHsin Su,
HongLin Chan,
ShengHao Lin,
ChinSan Liu,
ShihChao Lin,
ChiChen Lin,
ChingHsiung Lin
Publication year - 2017
Publication title -
molecular medicine reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.727
H-Index - 56
eISSN - 1791-3004
pISSN - 1791-2997
DOI - 10.3892/mmr.2017.7480
Subject(s) - cd80 , cd86 , dendritic cell , lipopolysaccharide , microbiology and biotechnology , cd40 , mixed lymphocyte reaction , tumor necrosis factor alpha , biology , immune system , nitric oxide , cytokine , flow cytometry , t cell , immunology , in vitro , cytotoxic t cell , biochemistry , endocrinology
The dendritic cell (DC) maturation process is essential for the development of T cell responses and immune tolerance. Accordingly, DCs are considered a major target in the development of immunomodulating agents. In the present study, the effect of sinulariolide, an active compound isolated from the cultured soft coral Sinularia flexibilis, on lipopolysaccharide (LPS)‑induced murine bone marrow‑derived DCs was evaluated. The different phenotypes, cytokine secretion and the mix‑lymphocyte reaction of DCs were detected using flow cytometry and ELISA. The experimental results revealed that the phenotypic and functional maturation of DCs stimulated by LPS were markedly reduced by sinulariolide in a concentration‑dependent manner, including the expression of co‑stimulatory molecules (CD40, CD80 and CD86). In addition, sinulariolide reduced the release of tumor necrosis factor‑α, interleukin (IL)‑6, IL‑12 and nitric oxide from the LPS‑activated DCs, decreased their abilities to stimulate allogeneic T cell proliferation, and inhibited LPS‑induced nuclear factor‑κB pathways. These findings offer novel insight into the immunopharmacological function of sinulariolide and its effects on DCs.
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