Immunomodulatory effect of low molecular-weight seleno-aminopolysaccharide on immunosuppressive mice

Int J Biol Macromol. 2019 Feb 15:123:1278-1288. doi: 10.1016/j.ijbiomac.2018.10.099. Epub 2018 Oct 17.

Abstract

Low molecular-weight seleno-aminopolysaccharides (LSA) have been shown to possess a variety of biological activities in vitro. In the present study, we further investigated the immunomodulatory effect of LSA on immunosuppressive mice induced by cyclophosphamide (CPA) and its molecular mechanism. The results demonstrated that LSA could significantly increase spleen and thymus indices, proliferation of splenic lymphocyte, the secretion of cytokines (IL-2, IL-4, IL-10 and INF-γ) of serum and ileum, and secretory immunoglobulin A (sIgA) content of small intestine. LSA dramatically improved the gene expression levels of IL-2, IL-4, IL-10 and INF-γ in small intestine by real-time fluorescent quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Furthermore, our data indicated that LSA could significantly increase the gene expression levels of IL-1β and iNOS in RAW264.7 cells. LSA was further shown to remarkably promote inhibitor kappa Bα (IκBα) and nuclear factor-kappa B (NF-κB) p65 phosphorylation with western blot analysis. Taken together, these findings suggest that LSA has immunomodulatory activity on immunosuppressive mice and macrophage RAW264.7 cells, and its mechanism may be related to activation of NF-κB signaling pathway.

Keywords: Immunomodulatory activity; Low molecular seleno-aminopolysaccharide; NF-κB signaling pathway.

MeSH terms

  • Amines / pharmacology*
  • Animals
  • Body Weight / drug effects
  • Cell Proliferation / drug effects
  • Cytokines / blood
  • Cytokines / genetics
  • Ileum / metabolism
  • Immunoglobulin A, Secretory / metabolism
  • Immunologic Factors / pharmacology*
  • Immunosuppression Therapy*
  • Lymphocytes / cytology
  • Lymphocytes / drug effects
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Molecular Weight
  • NF-kappa B / metabolism
  • Nitric Oxide / metabolism
  • Organ Specificity / drug effects
  • Polysaccharides / pharmacology*
  • RAW 264.7 Cells
  • Selenium / pharmacology*
  • Signal Transduction
  • Spleen / cytology

Substances

  • Amines
  • Cytokines
  • Immunoglobulin A, Secretory
  • Immunologic Factors
  • NF-kappa B
  • Polysaccharides
  • Nitric Oxide
  • Selenium