# Moon Jellyfish Mucin and Collagen Attenuate Catabolic Activity in Chondrocytes but Show Limited Efficacy in an Osteoarthritis Rat Model

**Authors:** Haruka Omura, Eriko Toyoda, Takayuki Baba, Ryoka Uchiyama, Masahiko Watanabe, Masato Sato

PMC · DOI: 10.3390/ijms262210920 · International Journal of Molecular Sciences · 2025-11-11

## TL;DR

Moon jellyfish mucin and collagen may help protect cartilage in lab tests but had limited success in treating osteoarthritis in rats.

## Contribution

Moon jellyfish mucin and collagen show potential for cartilage repair without hyaluronic acid.

## Key findings

- JM and JC affected gene expression related to cartilage in lab-grown chondrocytes.
- Injections of JM alone did not significantly reduce cartilage degeneration in OA rats.
- Further research is needed to optimize treatment conditions for in vivo effectiveness.

## Abstract

Cartilage regeneration has long been a major challenge in the treatment of osteoarthritis (OA). Aiming to develop a simple outpatient treatment for knee OA, we have demonstrated the potential of combining Nomura’s jellyfish mucin (JM) and hyaluronic acid (HA) to contribute to cartilage repair and regeneration in chondrocytes. In this study, we examined the effects of moon jellyfish JM and jellyfish collagen (JC) on chondrocytes. Polydactyly-derived chondrocytes (PDs), obtained from polydactyly surgery, were used. PDs were cultured in media supplemented with JM or JC, harvested, and evaluated by RT-qPCR. The effects of simultaneous addition of the inflammatory cytokine IL-1β were also examined. Furthermore, the effects on rat articular cartilage were investigated. A mono-iodoacetate (MIA) model was created by intra-articular injection in 6-week-old rats, followed by four intra-articular injections. Evaluations were performed using macroscopic observation and histological assessment with the OARSI scoring system. In vitro, the addition of JM or JC significantly affected the expression of ACAN, MMP3, and ADAMTS5. However, in vivo, intra-articular injection of JM alone did not significantly suppress cartilage degeneration in MIA-induced OA model rats. Both JM and JC may contribute to the suppression of cartilage degeneration as well as to cartilage repair and regeneration, even in the absence of HA. However, further studies are needed to clarify the optimal conditions, such as dosage, timing, and delivery method, that are required to achieve these effects in articular cartilage.

## Linked entities

- **Genes:** ACAN (aggrecan) [NCBI Gene 176], MMP3 (matrix metallopeptidase 3) [NCBI Gene 4314], ADAMTS5 (ADAM metallopeptidase with thrombospondin type 1 motif 5) [NCBI Gene 11096]
- **Proteins:** IL1B (interleukin 1 beta)
- **Chemicals:** mono-iodoacetate (PubChem CID 5240)
- **Diseases:** osteoarthritis (MONDO:0005178), polydactyly (MONDO:0021003)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Acan (aggrecan) [NCBI Gene 58968] {aka Agc, Agc1}, Slc13a2 (solute carrier family 13 member 2) [NCBI Gene 65202] {aka Nadc1, mucin}, Adamts5 (ADAM metallopeptidase with thrombospondin type 1 motif, 5) [NCBI Gene 304135], Mmp3 (matrix metallopeptidase 3) [NCBI Gene 171045] {aka MMP-3, SL-1}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}
- **Diseases:** Polydactyly (MESH:D017689), cartilage degeneration (MESH:D002357), OA (MESH:D010003), inflammatory (MESH:D007249), knee OA (MESH:D020370)
- **Chemicals:** HA (MESH:D006820), MIA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12652806/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12652806/full.md

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Source: https://tomesphere.com/paper/PMC12652806