Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit Robust Antifibrotic Potential and Ameliorates Mouse Liver Fibrosis.
Ja Sung ChoiYoung-Jin ParkSung-Whan KimPublished in: Cell transplantation (2021)
Recently, three-dimensional (3D)-cultured adipose mesenchymal stem cells (ASCs) have provided an effective therapy for liver fibrosis. This study aimed to enhance the potential of human ASCs for antifibrosis or hepatocyte regeneration using a 3D culture system and investigate their therapeutic mechanism in experimental liver fibrosis. ASC-3Dc were generated in a 3D culture system and stimulated with four growth factors, namely epidermal growth factor, insulin-like growth factor (IGF)-1, fibroblast growth factor-2, and vascular endothelial growth factor-A. The expression levels of antifibrotic or hepatic regeneration factors were then measured using quantitative real-time polymerase chain reaction and enzyme-linked immunosorbent assay. The therapeutic effects of ASC-3Dc were determined using a liver fibrosis model induced by thioacetamide. Histological analysis was performed to elucidate the therapeutic mechanism. ASC-3Dc exhibited high levels of hepatocyte growth factor (HGF), IGF-1, stromal cell-derived factor (SDF)-1 genes, and protein expression. In addition, injecting ASC-3Dc significantly prevented hepatic fibrosis and improved liver function in vivo. Moreover, high numbers of ki-67-expressing hepatocytes were detected in the ASC-3Dc-injected livers. Albumin-expressing ASC-3Dc engrafted in fibrotic livers augmented HGF expression. Thus, short-term 3D-cultured ASCs may be a novel alternative to the conventional treatment for liver damage in clinical settings.
Keyphrases
- liver fibrosis
- growth factor
- endothelial cells
- dendritic cells
- mesenchymal stem cells
- vascular endothelial growth factor
- nlrp inflammasome
- stem cells
- poor prognosis
- binding protein
- umbilical cord
- adipose tissue
- squamous cell carcinoma
- induced pluripotent stem cells
- oxidative stress
- systemic sclerosis
- high throughput
- long non coding rna
- pi k akt
- mouse model
- gene expression
- pluripotent stem cells
- human health
- cell therapy
- signaling pathway
- mass spectrometry
- wild type