FGF21-modified adipose stem cell-derived exosomes promote wound healing by activating fibroblast glycolysis through AMPK/mTOR signaling.
What this study shows
FGF21-enriched exosomes from engineered ADSCs promote chronic wound healing by activating fibroblast glycolysis, with AMPK activated and mTOR signaling suppressed, improving proliferation, migration, and tissue repair in a mouse model.
At a glance
| Evidence type | A Animal model Marked A because it is an animal intervention or observation study measuring an organismal outcome (model: Mouse + Human fibroblasts); the code names the system studied -- animal work can be rigorous and still not be human data. |
| Study type | 4 - Animal Study |
| Model system | Mouse + Human fibroblasts |
| Journal | Cellular signalling |
| Year | 2026 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1016/j.cellsig.2026.112742 · PMID 42551612 |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | FGF21-modified ADSC exosomes |
| Target | AMPK/mTOR |
| Model | Mouse + Human (fibroblasts in vitro) |
| Effect | Promotes wound healing via fibroblast glycolysis, with AMPK activated and mTOR signaling suppressed |
In the Atlas
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