EBioMedicine · 2016 · 455 citations · 22 references
Veterinary MedicineBiomedical SciencesImmunologyInflammationInnate ImmunityWound HealingAcute InflammationBurn PathophysiologyCytokine BiologyInflammatory Cell ResponsesInflammatory Cell SignalingInflammatory SignalingBurn Injury PathophysiologyExosome CharacterizationExosome-based TherapyInflammation In Burn WoundsInflammation In Wound HealingInflammatory Response In BurnsMicrorna In InflammationMicrorna Regulation Of Inflammation
Mesenchymal stem cell (MSC)-derived exosomes have diverse functions in regulating wound healing and inflammation; however, the molecular mechanism of human umbilical cord MSC (hUCMSC)-derived exosomes in regulating burn-induced inflammation is not well understood. We found that burn injury significantly increased the inflammatory reaction of rats or macrophages exposed to lipopolysaccharide (LPS), increased tumor necrosis factor α (TNF-α) and interleukin-1β (IL-1β) levels and decreased IL-10 levels. hUCMSC-exosome administration successfully reversed this reaction. Further studies showed that miR-181c in the exosomes played a pivotal role in regulating inflammation. Compared to control hUCMSC-exosomes, hUCMSC-exosomes overexpressing miR-181c more effectively suppressed the TLR4 signaling pathway and alleviated inflammation in burned rats. Administration of miR-181c-expressing hUCMSC-exosomes or TLR4 knockdown significantly reduced LPS-induced TLR4 expression by macrophages and the inflammatory reaction. In summary, miR-181c expression in hUCMSC-exosomes reduces burn-induced inflammation by downregulating the TLR4 signaling pathway.
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Krisztián Németh, Asada Leelahavanichkul, Peter S.T. Yuen et al. · Nature Medicine · 2008 · 2.4K citations · Full text
Exosome-delivered microRNAs modulate the inflammatory response to endotoxin
Margaret Alexander, Ruozhen Hu, Marah C. Runtsch et al. · Nature Communications · 2015 · 767 citations · Full text