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Immunomodulatory activity of macromolecular polysaccharide isolated from Grifola frondosa
Xiao-Lei Ma1, Meng Meng1, Li-Rong Han1
1Key Laboratory of Food Nutrition and Safety, Ministry of Education, College of Food Engineering and Biotechnology, Tianjin University of Science & Technology, Tianjin 300072, China.
Abstract:
The present study was designed to evaluate the immune-modulating effects of the polysaccharide from Grifola frondosa (GFP) by using mouse peritoneal macrophage and cytoxan (CTX) induced immunosuppression models. Our results from the phagocytotic and mononuclear phagocytic system function assays showed that GFP-A (one component from GFP) stimulated the phagocytosis of the phagocytes. The splenocyte proliferation assay showed that GFP-A acted the effect combing ConA or LPS in splenocyte proliferation. The results showed that GFP-A increased indices of thymus and spleen, the levels of LDH and ACP in the spleen, the mRNA levels of IL-1β, IL-2, IL-6 and IFN-γ in splenocyte. And GFP-A also significantly increased the expression of CD4(+) and CD8(+) splenic T lymphocytes, which were suppressed by the CTX in peripheral blood. In conclusion, our results indicate that the GFP-A is involved in immunomodulatory effects leading to its modulatory effects on immunosuppression.
Insights
Grifola frondosa polysaccharide (GFP-A) enhances immune function by stimulating phagocytosis and splenocyte proliferation. This component also boosts thymus and spleen indices, cytokine production, and T lymphocyte expression, counteracting immunosuppression.
Area of Science:
- Immunology
- Pharmacology
- Mycology
Background:
- Immunosuppression is a critical condition affecting immune system function.
- Grifola frondosa polysaccharides (GFP) are known for potential biological activities.
- Understanding the specific immune-modulating effects of GFP components is crucial.
Purpose of the Study:
- To evaluate the immune-modulating effects of a Grifola frondosa polysaccharide component (GFP-A).
- To investigate GFP-A's efficacy in a cytoxan (CTX)-induced immunosuppression mouse model.
- To determine GFP-A's impact on phagocytosis, splenocyte proliferation, and immune cell populations.
Main Methods:
- Mouse peritoneal macrophage and CTX-induced immunosuppression models were utilized.
- Phagocytotic and mononuclear phagocytic system function assays were performed.
- Splenocyte proliferation assays, thymus and spleen index measurements, and analysis of cytokine mRNA and T lymphocyte expression were conducted.
Main Results:
- GFP-A significantly stimulated phagocytosis and splenocyte proliferation, particularly when combined with ConA or LPS.
- Administration of GFP-A increased thymus and spleen indices and altered spleen enzyme levels (LDH, ACP).
- GFP-A elevated mRNA levels of IL-1β, IL-2, IL-6, and IFN-γ, and increased CD4(+) and CD8(+) T lymphocyte expression in splenocytes, counteracting CTX-induced suppression.
Conclusions:
- The study demonstrates that GFP-A possesses significant immune-modulating properties.
- GFP-A effectively enhances cellular and humoral immune responses.
- These findings suggest GFP-A has potential as a therapeutic agent for counteracting immunosuppression.
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