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Exosomal miR-103a-3p from Crohn's creeping fat-derived ASCs contributes to intestinal fibrosis by targeting TGFBR3 and activating fibroblasts.

Wenwei QianYihan XuWeiwei WenLiang-Yu HuangZhen GuoWeiming ZhuYi Li
Published in: Journal of Crohn's & colitis (2023)
Our findings showed that exosomal miR-103a-3p from CF-ASCs promotes intestinal fibrosis by activating fibroblasts via TGFBR3 targeting, suggesting that CF-ASCs are potential therapeutic targets for intestinal fibrosis in CD.
Keyphrases
  • cystic fibrosis
  • signaling pathway
  • extracellular matrix
  • adipose tissue
  • liver fibrosis
  • fatty acid
  • drug delivery