Application of Gelatin Bioinks and Cell-Printing Technology to Enhance Cell Delivery Capability for 3D Liver Fibrosis-on-a-Chip Development.
Hyungseok LeeJongmin KimYeongjin ChoiHyungseok LeePublished in: ACS biomaterials science & engineering (2020)
Liver fibrosis is a critical liver disease which can lead to liver cirrhosis, cancer, and liver failure. Among various etiological factors, activated stellate cells are a major factor that can induce liver fibrosis. Several studies have presented in vitro models to identify drugs for liver fibrosis; however, there are still limitations in terms of the 2D culture conditions, random co-culture of liver cells, and lack of extracellular matrix components. Therefore, a 3D liver fibrosis-on-a-chip was developed with three liver cell types (hepatocytes, activated stellate cells, and endothelial cells) using a novel cell-printing technique with gelatin bioinks, which were used to deliver each nonparenchymal liver cell type as a multilayer construct. Liver fibrosis-specific gene expression, collagen accumulation, cell apoptosis, and reduced liver functions caused by activated stellate cells were also evaluated. Furthermore, previously reported chemicals were added to the 3D liver fibrosis-on-a-chip to examine the downregulation of activated hepatic stellate cells. In conclusion, the developed 3D liver fibrosis-on-a-chip could be used as a potential in vitro model in the research field.
Keyphrases
- liver fibrosis
- induced apoptosis
- gene expression
- cell cycle arrest
- single cell
- endothelial cells
- extracellular matrix
- high throughput
- cell death
- squamous cell carcinoma
- dna methylation
- cell proliferation
- circulating tumor cells
- stem cells
- endoplasmic reticulum stress
- hepatitis b virus
- oxidative stress
- mesenchymal stem cells