Vinpocetine Inhibited the CpG Oligodeoxynucleotide-induced Immune Response in Plasmacytoid Dendritic Cells

ABSTRACT

Plasmacytoid dendritic cells (pDCs) exert dual roles in immune responses through inducing inflammation and maintaining immune tolerance. A switch of pDC phenotype from pro-inflammation to tolerance has therapeutic promise in the treatment of autoimmune diseases. Vinpocetine, a vasoactive vinca alkaloid extracted from the periwinkle plant, has recently emerged as an immunomodulatory agent. In this study, we evaluated the effect of vinpocetine on phenotype of pDCs isolated from C57BL/6 mice and explored its possible mechanism. Our data showed that vinpocetine significantly downregulated the expression of CD40, CD80, and CD86 on pDCs and increased the expression of translocator protein (TSPO), the specific receptor of vinpocetine, in pDCs. Vinpocetine significantly inhibited the Toll-like receptor 9 signaling pathway and reduced the secretion of related cytokines in pDCs through TSPO. Furthermore, viability of pDCs was significantly promoted by vinpocetine. These findings imply that vinpocetine serves as an immunomodulatory agent for pDCs and may be applied for the treatment of pDCs-related autoimmune diseases.

KEYWORDS:

• Immunomodulation
• plasmacytoid dendritic cells
• vinpocetine

Declaration of interest

The authors declare no competing interests.

Funding

This work was supported by the National Natural Science Foundation of China (81301072, 81271398), the Promotive Research Fund for Excellent Young and Middle-aged Scientists of Shandong Province (BS2013YY021), Shandong Province Natural Science Fund Project (ZR2014HL035), the Science and Technology Development Project of Jining City, Shandong Province, China (2014jnnk20, [2015]57-69), Nursery Programme of Affiliated Hospital of Jining Medical University (MP-2015-018) and the Scientific Research Fund of Jining Medical University (JY2013KJ039).