To discuss the molecular mechanism of immunoenhancing activities of Hyriopsis cumingii polysaccharides (HCPS), influences of HCPS on mice immunosignaling molecules (IL-2, IL-10, IFN-γ, NO, cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP)) and T lymphocyte differentiation (to CD4 + and CD8+ T cells) were evaluated by cell model in vitro and/or cyclophosphamide-induced immunosuppression animal model in vivo. Results showed that gastric gavage of crude HCPS could promote the production of IL-2, IFN-γ, inducible nitric oxide synthase (iNOS), cGMP, CD4 and CD8 in a dose-dependent manner. While, crude HCPS by gastric gavage exhibited suppressive effects on the production of IL-10 and cAMP in a dose-dependent manner. Crude HCPS and its purified fractions (HCPS-1, HCPS-2 and HCPS-3) could strengthen peritoneal macrophage expressing iNOS in vitro in a dose-dependent manner. HCPS-stimulated immunostrengthening functions was mediated, at least in part, by immunosignaling molecules of IL-2, IL-10, IFN-γ, NO, cAMP and cGMP, and T lymphocyte differentiation (to CD4+ and CD8+ T cells).
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