Level D· Scientific groundwork from lab and animal studiesLaboratory StudyPubMed

Optimised cryopreservation preserves functional competence of goat adipose-derived mesenchymal stem cells and is associated with stress-adapted mitochondrial and paracrine features.

Abraham M., Kori I., Anusha PV., Fathima I., Idris MM., Goel S.

Laboratory Study on Chronic Wound, published in J Tissue Eng (2026) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
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This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Laboratory Study
Journal
J Tissue Eng (2026)
Country
England
Reported sample size
—
Source database
PubMed
PMID
42591700
DOI
10.1177/20417314261473533

Abstract (original English)

Cryopreservation is essential for mesenchymal stem cell banking, but its effects on adipose-derived stem cell (ADSC) function remain debated. This study evaluated an optimised cryopreservation protocol for goat ADSCs using phenotypic, functional, mitochondrial-associated, conditioned-medium, proteomic, and wound-healing assays. Cryopreserved ADSCs retained morphology, viability, clonogenicity, proliferation, adherence, immunophenotype, and trilineage differentiation, comparable to those of fresh ADSCs. Post-thaw cells showed increased MitoTracker Green signal, JC-1 red/green ratio, ATP content, relative mtDNA abundance, and SOD2-associated immunofluorescence, together with lower H 2 O 2 -induced ROS- and autophagy-associated fluorescence. Conditioned-medium proteomics suggested exploratory shifts toward extracellular matrix-, anti-protease-, and redox-associated proteins. Functionally, cryopreserved ADSCs maintained inflammatory cue-directed migration, modulated macrophage surface marker expression, and reduced oxidative stress-associated injury readouts in goat dermal fibroblasts. In a goat excisional wound model, ADSC treatment improved wound-closure kinetics and supported histological repair. Overall, optimised cryopreservation preserved the functional competence of goat ADSCs and was associated with stress-adapted post-thaw features.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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