Human Wharton's jelly mesenchymal stem cells protect neural cells from oxidative stress through paracrine mechanisms
Puig-Pijuan T., de Godoy MA., Pinheiro Carvalho LR., Bodart-Santos V., Lindoso RS., Pimentel-Coelho PM.
Laboratory Study on Immune Modulation, published in Future Sci OA (2020) — summary generated from the PubMed abstract.
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
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
- Future Sci OA (2020)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 33235812
- PMCID
- PMC7668126
- DOI
- 10.2144/fsoa-2020-0036
- Citations
- 14
Abstract (original English)
Aim Mesenchymal stem cells (MSCs) have neuroprotective and immunomodulatory properties, which are partly mediated by extracellular vesicles (EVs) secretion. We aimed to evaluate the effects of human Wharton's jelly-derived MSCs (WJ-MSCs) and their EVs on rat hippocampal cultures subjected to hydrogen peroxide (H 2 O 2 ). Materials & methods Hippocampal dissociated cultures were either co-cultured with WJ-MSCs or treated with their EVs prior to H 2 O 2 exposure and reactive oxygen species levels and cell viability were evaluated. Results Coculture with WJ-MSCs or pre-incubation with EVs prior to the insult reduced reactive oxygen species after H 2 O 2 exposure. Cell viability was improved only when coculture was maintained following the insult, while EVs did not significantly improve cell viability. Conclusion WJ-MSCs have potential antioxidant and neuroprotective effects on hippocampal cultures which might be partially mediated by EVs.
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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