Level D· Scientific groundwork from lab and animal studiesLaboratory StudyPubMed

Alpha Lipoic Acid Promotes the Proliferation, Motility, and Antioxidant Defense System of Human Adipose-Derived Stromal/Stem Cells.

Uslu G., Halbutoğulları ZS.

Laboratory Study on Chronic Wound, Immune Modulation, published in Cell Biochem Funct (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
Read the A–D evidence level guide

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
Cell Biochem Funct (2026)
Country
England
Reported sample size
—
Source database
PubMed
PMID
41560338
DOI
10.1002/cbf.70167
Citations
1

Abstract (original English)

Adipose-derived stromal/stem cells (ASCs) are a readily accessible mesenchymal stem cell population with high regenerative and immunomodulatory potential. Despite their regenerative potential, ASCs experience replicative senescence during in vitro expansion, resulting in oxidative damage and impaired cellular function. Alpha-lipoic acid (ALA) is a potent antioxidant with reported anti-aging and cytoprotective effects in various cell types. This study aimed to investigate the effects of ALA on proliferation, migration, invasion capacity, and oxidative stress response of primary human ASCs in vitro. Human ASCs were isolated from adipose tissue samples and characterized via flow cytometry and multilineage differentiation. The safe and effective concentration of ALA was determined using WST-1 cell viability assays. Functional evaluations included wound healing and invasion assays. Gene expression of stemness, proliferation, cell cycle, migration, and apoptosis markers was analyzed by qRT-PCR, while MMP2 and MMP9 protein expression was assessed by immunofluorescence. Cellular oxidative stress levels were measured using DCF-DA flow cytometry, and cytotoxicity was evaluated with the LDH release assay. ALA supplementation significantly enhanced ASC proliferation (p < 0.01), migration (p < 0.001), and invasion (p < 0.01). Upregulation of MMP2 (p < 0.001) and MMP9 (p < 0.001) proteins wa

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.

How we grade evidence
HumansThioctic AcidCell ProliferationCell MovementAntioxidantsAdipose TissueMesenchymal Stem CellsOxidative StressCells, CulturedMatrix Metalloproteinase 2

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