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• W2896645751 startingPage "2266" @default.
• W2896645751 abstract "In vitro engineering of liver tissue is a rapidly developing field for various biomedical applications. However, liver tissue culture is currently performed on only a small scale with a low density of hepatocytes. In this study, a simple design was introduced in a liver microsystem to enhance the transport of nutrients (e.g., oxygen and glucose) for the three-dimensional large-scale, high-density culture of hepatocytes. In this design, convection across the cell culture zone was generated to mimic sinusoid blood flow (SBF) based on the pressure difference between two fluids flowing in a countercurrent manner on either side of the cell culture zone. First, the distributions of living and dead cells in different culture subzones under various perfusion flow rates were observed, analysed, and compared. Then, the enhanced transport of nutrients was experimentally validated in relation to the viability of cells and theoretically explained by comparing the fluid velocity and oxygen concentration distribution in the cell culture zone in counterflow and coflow modes. Finally, the functions of the SBF-mimicked liver microsystem were assessed on the basis of specific metabolites, synthesized proteins, and bilirubin detoxification of hepatocytes, with collagen and alginate as extracellular matrices. Under this design, the density of hepatocytes cultured at the 3-mm-thickness scale reached ~7 × 107 cells/ml on Day 7, and the metabolism and detoxification functions of the cells worked well. In addition, a liver rope-like structure and sphere-like clusters of cells were observed. This work provides insight for the design of a bionic liver microsystem." @default.
• W2896645751 created "2018-10-26" @default.
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• W2896645751 date "2018-11-13" @default.
• W2896645751 modified "2023-10-15" @default.
• W2896645751 title "Large‐scale high‐density culture of hepatocytes in a liver microsystem with mimicked sinusoid blood flow" @default.
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• W2896645751 doi "https://doi.org/10.1002/term.2758" @default.
• W2896645751 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30350403" @default.
• W2896645751 hasPublicationYear "2018" @default.
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