# SC2-3, a Marine Nutrient Glycopeptide from Nereis succinea: Alleviating Cyclophosphamide-Induced Immunocompromise in Mice via M1-Type Macrophage Polarization

**Authors:** Yulin Liu, Yanan Huang, Jiaqi Li, Yiping Zhang, Peipei Wang

PMC · DOI: 10.3390/foods15050874 · Foods · 2026-03-04

## TL;DR

A marine glycopeptide from Nereis succinea helps restore immune function in mice weakened by a drug, by activating specific immune cells and protecting the gut.

## Contribution

SC2-3 is a novel marine glycopeptide shown to alleviate immunocompromise via M1 macrophage polarization and intestinal barrier protection.

## Key findings

- SC2-3 elevated immune markers and repaired tissue damage in cyclophosphamide-treated mice.
- SC2-3 induced M1 macrophage activation and upregulated pro-inflammatory cytokines.
- SC2-3 maintained intestinal barrier integrity by regulating tight junction proteins and MUC-2.

## Abstract

Immunodeficiency is a global health concern, partly due to disrupted rhythms and drugs. Marine glycopeptides, with immunomodulatory and intestinal barrier protective activities, show great potential in dietary supplements and functional foods. Here, a marine glycopeptide, SC2-3, with a molecular weight of 5061 Da, was isolated and purified from Nereis succinea. Monosaccharide composition, NMR data, amino acid composition analysis, and SDS-PAGE analyses identified SC2-3 as a glycopeptide. The N-glycome results of SC2-3 collected by MALDI-TOF-MS revealed that SC2-3 contains fucosylated N-glycans with shorter glycan chains compared to human-derived N-glycans. SC2-3 exerted a significant immune-enhancing effect on macrophages in vitro. In vivo, in cyclophosphamide-induced immunocompromised mice, SC2-3 at different concentrations elevated organ indices, blood cell counts, and serum levels of IL-1β, TNF-α, and IL-6, while repairing cyclophosphamide-damaged/atrophied tissues. Mechanistically, SC2-3 induced the differentiation of RAW264.7 cells toward an M1-like activation profile, significantly promoting the release of NO and ROS, upregulating the secretion of pro-inflammatory cytokines (IL-1β, TNF-α, and IL-6), and activating the TLR4/NF-κB signaling pathway. Additionally, SC2-3 upregulated intestinal epithelial tight junction proteins and normalized the overexpression of MUC-2, thereby maintaining intestinal barrier integrity. These findings indicated the potential efficacy of the glycopeptide SC2-3 derived from natural marine sources in immunomodulation and protection of intestinal health.

## Linked entities

- **Proteins:** TLR4 (toll like receptor 4), NFKB1 (nuclear factor kappa B subunit 1), MUC2 (mucin 2, oligomeric mucus/gel-forming)
- **Chemicals:** cyclophosphamide (PubChem CID 2907), SC2-3 (PubChem CID 496893)
- **Diseases:** immunodeficiency (MONDO:0021094)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Muc2 (mucin 2) [NCBI Gene 17831] {aka 2010015E03Rik, MCM, wnn}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}
- **Diseases:** Immunodeficiency (MESH:D007153), inflammatory (MESH:D007249)
- **Chemicals:** glycan (MESH:D011134), N (MESH:D009584), Cyclophosphamide (MESH:D003520), SDS (MESH:D012967), NO (MESH:D009614), amino acid (MESH:D000596), Glycopeptide (MESH:D006020), N-glycans (-)
- **Species:** Alitta succinea (species) [taxon 981110], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12984555/full.md

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Source: https://tomesphere.com/paper/PMC12984555