LL-37 plus stem cells speeds diabetic wound closure in mice
Researchers report exosomal transfer of NRROS from LL-37-primed adipose stem cells activates TGF-beta/SMAD and Hippo/TEAD1 signaling in fibroblasts.
PR
By Priya Raman · Science Reporter
Sep 17 21:51 ETSource: Cytokine
The wire
- 01In a diabetic mouse wound model, LL-37 combined with adipose-derived stem cells healed wounds faster than either treatment alone, with LL-37 raising stem cell viability dose-dependently.
- 02Human diabetic wound samples showed deficiency of cathelicidin (CAMP), the LL-37 precursor, offering a rationale readers tracking LL-37 can weigh against gray-market wound-healing claims.
- 03The work is animal and in vitro only, published in Cytokine, with no human dosing, safety or delivery data for the combination.
From the source
Read at pubmed.ncbi.nlm.nih.govCombinatorial therapy of LL-37 and ADSCs accelerates diabetic wound repair by orchestrating NRROS-mediated crosstalk between TGF-β/SMAD and hippo/TEAD1 axes
Cytokine · 2026 Nov · Wei L, Wang L, Zhong F et al.
Source URL https://pubmed.ncbi.nlm.nih.gov/42641316/