# Restoration of tendon repair microenvironment by grapefruit exosome-loaded microneedle system for tendinopathy therapy

**Authors:** Yuan Zhang, Ruiyang Zhang, Ti Zhang, Yuhao Mu, Talante Juma, Xu Li, Hao Li, Quanyi Guo, Yongping Cao

PMC · DOI: 10.3389/fbioe.2025.1615650 · Frontiers in Bioengineering and Biotechnology · 2025-07-28

## TL;DR

A microneedle patch loaded with grapefruit exosomes helps repair tendons by reducing inflammation and promoting tissue regeneration in mice.

## Contribution

A novel grapefruit exosome-loaded microneedle system is introduced for targeted tendon repair.

## Key findings

- GF-Exos enhanced tenocyte proliferation and collagen I synthesis while polarizing macrophages to M2 phenotypes.
- MN@GF-Exos improved gait recovery and extracellular matrix remodeling in a mouse model of tendinopathy.
- The treatment reduced fibrosis and maintained systemic safety with normal organ histology and serum biomarkers.

## Abstract

Tendinitis repair remains challenging due to the limited self-renewal capacity of tenocytes and persistent inflammatory microenvironment. Conventional therapies remain limited by systemic drug toxicity and fail to coordinate immunomodulation with matrix remodeling. Plant-derived extracellular vesicles have demonstrated tissue repair potential owing to their unique bioactive components and exceptional cross-species compatibility. Nevertheless, their therapeutic role in tendon matrix regeneration remains underexplored. Here, we developed a grapefruit-derived exosome-loaded microneedle patch (MN@GF-Exos) to synergistically restored tendon structure and functions. Grapefruit-derived exosomes (GF-Exos) were loaded into dissolvable hyaluronic acid microneedles (MNs) for sustained release. GF-Exos reversed oxidative stress in tenocytes, enhancing cellular proliferation and migration, restoring collagen I synthesis, and polarizing macrophages toward M2-repair phenotypes. Transcriptomics revealed GF-Exos modulated cytokine-cytokine receptor interactions, suppressing inflammation-related pathways and activating ECM organization genes. In collagenase-induced tendinopathy mice, MN@GF-Exos enhanced gait recovery and extracellular matrix remodeling. Histology confirmed reduced fibrosis without ectopic ossification. Systemic safety was validated by unchanged organ histology and within-normal-limits serum biomarkers. This dual-functional system leverages plant exosomes’ multi-component synergy and MN’s spatiotemporal control, offering a translatable strategy for chronic tendon regeneration.

## Linked entities

- **Chemicals:** collagenase (PubChem CID 75007581)
- **Diseases:** tendinopathy (MONDO:0100010), tendinitis (MONDO:0004857)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** inflammation (MESH:D007249), fibrosis (MESH:D005355), ectopic ossification (MESH:D009999), Tendinitis (MESH:D052256), toxicity (MESH:D064420)
- **Chemicals:** hyaluronic acid (MESH:D006820), GF (MESH:C053914)
- **Species:** Citrus x paradisi (grapefruit, species) [taxon 37656], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12336195/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12336195/full.md

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Source: https://tomesphere.com/paper/PMC12336195