Evidence map›Paper›PMID 41970253›Full record

ArticleMaterials today. Bio2026

The mechanistic study of injectable hydrogel loaded with BMSC-exosomes in regulating the TGF-β/MMP axis to inhibit experimental myopia model.

Jingwen Hui, Xiongfeng Nie, Zheya Han, Yuhua Rui, Yuxi Bai, Jingxuan Geng, Wenguang Liu, Quanhong Han

Abstract read
In one paragraph

Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jingwen HuiNankai University Optometry and Vision Science Institute, Nankai University Affiliated Tianjin Eye Hospital, Tianjin, 300071, China.
Xiongfeng NieSchool of Material Science and Engineering, Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin, 300350, China.
Zheya HanTianjin Eye Hospital, Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin Eye Institute, Tianjin, 300020, China.
Yuhua RuiNankai University Optometry and Vision Science Institute, Nankai University Affiliated Tianjin Eye Hospital, Tianjin, 300071, China.
Yuxi BaiTianjin Eye Hospital, Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin Eye Institute, Tianjin, 300020, China.
Jingxuan GengTianjin Eye Hospital, Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin Eye Institute, Tianjin, 300020, China.
Wenguang LiuSchool of Material Science and Engineering, Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin, 300350, China.
Quanhong HanNankai University Optometry and Vision Science Institute, Nankai University Affiliated Tianjin Eye Hospital, Tianjin, 300071, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological myopia involves reduced collagen deposition and scleral thinning, leading to axial elongation-a process exacerbated by chronic inflammation that disrupts scleral extracellular matrix homeostasis. To address this, we developed an injectable microgel system based on methacrylated alginate (AlgMA) loaded with BMSC-derived exosomes for preventing myopia progression. The photocrosslinkable AlgMA hydrogel exhibited a compressive modulus of ∼10 kPa, providing mechanical support for scleral reinforcement, while its porous network facilitated sustained exosome release. Processing into microgels (AlgMA-MGs) via repeated extrusion through a 25-gauge needle significantly improved injectability of AlgMA hydrogel. Exosome-loaded AlgMA-MGs (Exos-AlgMA-MGs) enhanced fibroblast proliferation and migration, downregulated MMP-2, and upregulated collagen I synthesis via modulation of the TGF-β/MMP axis. In a guinea pig form-deprivation model, both AlgMA-MGs and Exos-AlgMA-MGs attenuated axial elongation in myopic eyes, with the Exos-AlgMA-MGs showing optimal efficacy over four weeks, attributable to the combined biomechanical and bioactive effects. Histological analysis further confirmed that Exos-AlgMA-MGs increased scleral thickness and downregulated the expression of inflammatory factors in myopic eyes, thereby achieving effective anti-scleral remodeling. These findings suggest that Exos-AlgMA-MGs represents a promising strategy for controlling myopia progression.

Indexed as

Anti-inflammationExosomesInjectable hydrogelMyopiaScleral remodeling

Identifiers

PMID41970253
PMCPMC13068834

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.