Exosome derived from human umbilical cord mesenchymal stem cell mediates MiR-181c attenuating burn-induced excessive inflammation

X Li, L Liu, J Yang, Y Yu, J Chai, L Wang, L Ma… - EBioMedicine, 2016 - thelancet.com
X Li, L Liu, J Yang, Y Yu, J Chai, L Wang, L Ma, H Yin
EBioMedicine, 2016thelancet.com
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 …
Abstract
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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