# Grifola frondosa Polysaccharides Alleviated Cyclophosphamide—Induced Intestinal Injury Based on Microbiota, Metabolite and Immune Axis Modulation

**Authors:** Jindi Wu, Guilu Chen, Dingfeng Chen, Haoran Zhang, Huirong Lv, Zhengshun Wen

PMC · DOI: 10.3390/foods14193376 · 2025-09-29

## TL;DR

Grifola frondosa polysaccharides help protect the intestines from chemotherapy damage by improving gut health and immunity.

## Contribution

This study reveals a new role for Grifola frondosa polysaccharides in mitigating chemotherapy-induced intestinal injury through microbiota and immune modulation.

## Key findings

- GFP treatment reduced body weight loss and organ atrophy in mice with CTX-induced intestinal injury.
- GFP increased goblet cell numbers and upregulated genes like ZO-1 and MUC2, which support intestinal barrier integrity.
- GFP modulated gut microbiota and increased metabolites like SCFAs, which are linked to improved intestinal immunity.

## Abstract

Grifola frondosa polysaccharides (GFP), which possess antitumor properties, can counteract intestinal injury induced by cyclophosphamide (CTX). The objective of this research was to evaluate the efficacy of GFP in protecting the intestinal barrier of mice and investigate the mechanisms behind this effect. Using a CTX-induced intestinal barrier injury model, we found that GFP treatment significantly alleviated body weight loss and organ atrophy, while enhancing serum IgG and IgM levels. Histological analysis showed that GFP effectively repaired the intestinal mucosal structure, increased goblet cell numbers, and led to an upregulation in the gene expression of ZO-1, Occludin, and MUC2. GFP modulated cytokine expression, including IFN-γ, IL-4, IL-10, and IL-22. According to 16S rDNA sequencing results, GFP enhanced the abundance of unclassified_Muribaculaceae while reducing the prevalence of Escherichia_Shigella. Furthermore, GFP elevated the concentrations of several metabolites, including SCFAs and pyridoxal, which are closely related to intestinal barrier protection and mucosal immunity. Overall, this study demonstrated that GFP has strong potential as an immune-enhancing adjuvant and may represent a promising intervention strategy to mitigate chemotherapy-induced intestinal injury.

## Linked entities

- **Genes:** TJP1 (tight junction protein 1) [NCBI Gene 7082], si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3) [NCBI Gene 103182021], MUC2 (mucin 2, oligomeric mucus/gel-forming) [NCBI Gene 4583], IFNG (interferon gamma) [NCBI Gene 3458], IL4 (interleukin 4) [NCBI Gene 3565], IL10 (interleukin 10) [NCBI Gene 3586], IL22 (interleukin 22) [NCBI Gene 50616]
- **Chemicals:** cyclophosphamide (PubChem CID 2907), pyridoxal (PubChem CID 1050)
- **Species:** Grifola frondosa (taxon 5627), unclassified Muribaculaceae (taxon 2006847)

## Full-text entities

- **Genes:** Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Muc2 (mucin 2) [NCBI Gene 17831] {aka 2010015E03Rik, MCM, wnn}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Igh-V7183 (immunoglobulin heavy chain (V7183 family)) [NCBI Gene 16059] {aka B9-scFv, IgG, IgH, IgVH1(VSG), VH7183, VI24H}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, Il22 (interleukin 22) [NCBI Gene 50929] {aka IL-22, IL-22a, ILTIFa, If2b1, Iltif}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}
- **Diseases:** weight loss (MESH:D015431), Intestinal Injury (MESH:D007410), atrophy (MESH:D001284)
- **Chemicals:** CTX (MESH:D003520), pyridoxal (MESH:D011730), GFP (-), SCFAs (MESH:D005232)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12523291/full.md

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Source: https://tomesphere.com/paper/PMC12523291