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Mesenchymal stem cell-derived extracellular vesicles attenuate periductal fibrosis by inhibiting Th17 differentiation in human liver multilineage organoids and Mdr2−/− mice

  • Wenyi Chen
  • , Xinyi Chen
  • , Feiqiong Gao
  • , Qigu Yao
  • , Sheng Cheng
  • , Qiaoling Pan
  • , Jiong Yu
  • , Jinfeng Yang
  • , Guanghua Ma
  • , Jintao Gong
  • , Qian Li
  • , Yunhua Chen
  • , Lee Wei Lim
  • , Ilia Stambler
  • , Georgina M. Ellison-Hughes
  • , Brun Ulfhake
  • , Robert Chunhua Zhao*
  • , Hongcui Cao*
  • *Corresponding author for this work
  • Zhejiang University
  • Chinese Academy of Sciences
  • Chinese Academy of Medical Sciences
  • Department of Biological Science
  • International Society on Aging and Disease
  • Bar-Ilan University
  • King's College London
  • Karolinska Institutet
  • Beijing Key Laboratory of New Drug Development and Clinical Trial of Stem Cell Therapy (BZ0381)

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)
28 Downloads (Pure)

Abstract

Primary sclerosing cholangitis (PSC) pathogenesis involves immune dysregulation, genetic factors, and bile duct pathology; however, a comprehensive pathogenesis model and effective therapeutic strategies remain limited. Here, we develop a novel human liver multilineage organoid (Mulorg) model combined with Mdr2−/− mice to investigate the pro-fibrotic role of T helper 17 cells (Th17) and the therapeutic potential of mesenchymal stem cell-derived extracellular vesicles (EVMSC) for PSC, particularly periductal fibrosis. EVMSC alleviates interleukin-17A (IL-17A)-induced fibrotic Mulorgs (FibHOs) and mitigates periductal fibrosis in Mdr2−/− mice by inhibiting Th17 differentiation, decreasing Th17 numbers, and lowering intrahepatic IL-17A levels. Functional assays, miRNA array, and CUT & Tag analyses reveal that EVs-derived hsa-miR-7977 targets NFKBIZ, repressing IκBζ translation to reduce IL-17A and its downstream targets involved in Th17 differentiation, IL-17 signaling, and bile secretion pathways. Moreover, miR-7977-enriched EVMSC efficiently reduces IL-17A+ cell percentages in fibrotic areas and improves periductal fibrosis in Mdr2−/− mice. Co-culture of FibHOs with Th17 found miR-7977 inhibits Th17 migration to the periductal fibrosis area, with distinct morphological differences observed between patient- and healthy-derived FibHOs. These findings demonstrate that EV-derived miR-7977 mitigates the periductal fibrosis microenvironment by inhibiting Th17 differentiation and migration, the former by targeting NFKBIZ, regulating IL-17A and IκBζ-targeted gene expression. This study clarifies Th17’s role in the PSC fibrotic microenvironment, underscores the modeling contributions of Mulorgs, and highlights EV-derived miR-7977’s potential to ameliorate Th17-related periductal fibrosis, offering insights and novel therapeutic avenues for PSC.

Original languageEnglish
Article number546
JournalJournal of Nanobiotechnology
Volume23
Issue number1
DOIs
Publication statusPublished - 28 Jul 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Extracellular vesicles
  • Liver fibrosis
  • Mdr2 mice
  • Mesenchymal stem cells
  • Organoids
  • Primary sclerosing cholangitis

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