Regulation of the exopolysaccharide from an anamorph of Cordyceps sinensis on dendritic cell sarcoma (DCS) cell line

Eur J Nutr. 2013 Mar;52(2):687-94. doi: 10.1007/s00394-012-0373-x. Epub 2012 May 19.

Abstract

Purpose: Cordyceps sinensis has been regarded as a precious tonic food and herbal medicine in China for thousands of years. The exopolysaccharide (EPS) from an anamorph of Cordyceps sinensis was found to have antitumor immunomodulatory activity. Mature dendritic cells play a role in initiating antitumor immunity, so we try to investigate the effects of EPS on the murine dendritic cell line DCS.

Methods: Flow cytometry was used to assay the expression levels of cell surface molecules including major histocompatibility complex (MHC)-II, CD40, CD80, and CD86 of DCS cells and their ability to take up antigens. The ability of DCS cells to activate the proliferation of CTLL-2 T cells was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) method. IL-12 and TNF-α levels were detected using ELISA. Western blotting was performed to estimate the levels of phosphorylated Janus kinase 2 (p-JAK2), phosphorylated signal transducer and activator of transcription 3 (p-STAT3), nuclear factor-κB (NF-κB) p65 and p105.

Results: EPS increased the expressions of MHC-II, CD40, CD80, and CD86 of DCS cells and up-regulated their ability to take up antigens. EPS also enhanced their ability to activate the proliferation of CTLL-2 T cells. IL-12 and TNF-α secreted from DCS cells were up-regulated after EPS treatment. Furthermore, EPS significantly caused the decline of p-JAK2 and p-STAT3, significantly increased levels of NF-κB p65 in the nucleus and decreased levels of NF-κB p105 in the cytoplasm.

Conclusions: EPS may induce DCS cells to exhibit mature characteristics, and the mechanism involved is probably related to the inhibition of the JAK2/STAT3 signal pathway and promotion of the NF-κB signal pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • B7-1 Antigen / genetics
  • B7-1 Antigen / metabolism
  • B7-2 Antigen / genetics
  • B7-2 Antigen / metabolism
  • Blotting, Western
  • CD40 Antigens / genetics
  • CD40 Antigens / metabolism
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cordyceps / metabolism*
  • Dendritic Cells / cytology
  • Dendritic Cells / drug effects*
  • Enzyme-Linked Immunosorbent Assay
  • Gene Expression Regulation
  • Immunologic Factors / pharmacology*
  • Immunomodulation
  • Interleukin-12 / genetics
  • Interleukin-12 / metabolism
  • Janus Kinase 2 / genetics
  • Janus Kinase 2 / metabolism
  • Major Histocompatibility Complex / genetics
  • Mice
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Phosphorylation
  • Polysaccharides / pharmacology*
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antineoplastic Agents
  • B7-1 Antigen
  • B7-2 Antigen
  • CD40 Antigens
  • Immunologic Factors
  • NF-kappa B
  • Polysaccharides
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Tumor Necrosis Factor-alpha
  • Interleukin-12
  • Jak2 protein, mouse
  • Janus Kinase 2