https://scholars.lib.ntu.edu.tw/handle/123456789/605955
標題: | HGF/heparin-immobilized decellularized liver matrices as novel hepatic patches for hepatocyte regeneration in an acute liver injury model | 作者: | Hsieh Y.-C Yin W.-R Xu Y.-Y YUNG-TE HOU |
關鍵字: | D-Galactosamine–induced liver injury;HGF/heparin-immobilized decellularized liver matrix;Liver regeneration;Lagrange multipliers;Polysaccharides;D-galactosamine;D-galactosamine–induced liver injury;Decellularized livers;Hepatocyte growth factor;Hepatocyte growth factor/heparin-immobilized decellularized liver matrix;Hepatocytes;Liver cirrhosis;Liver injuries;matrix;Diseases | 公開日期: | 2022 | 卷: | 180 | 來源出版物: | Biochemical Engineering Journal | 摘要: | Although liver cirrhosis is a common condition and cause of death, treatment methods remain limited; for example, instead of facilitating hepatocyte regeneration, they may only alleviate or resolve symptoms. Notably, studies have indicated that liver fibrosis is reversible; moreover, prompt and appropriate treatment can prevent liver fibrosis from developing into liver cirrhosis. In this study, a hepatocyte growth factor (HGF)/heparin-immobilized decellularized liver matrix (HGF/heparin-DLM) was fabricated for hepatocyte regeneration in a model of acute D-galactosamine–induced liver injury. Various initial concentrations (0.2, 0.4, 0.6, 0.8, 1 mg/mL) were used for the immobilization of heparin on DLM films. The amounts of immobilized heparin on the DLM films at these concentrations were 4.7 ± 1.1, 12.2 ± 2.7, 18.2 ± 5.1, 21.9 ± 3.8, and 29.1 ± 1.1 μg/cm2, respectively. The relative viability and albumin synthesis of the hepatocytes on the HGF/heparin-DLM films were 19% and 26% greater than those of the hepatocytes cultured in regular petri dishes on day 3, respectively. The LDH and albumin of the injured hepatocytes on the HGF/heparin-DLM films were 95% lower and almost 2.7 times higher than those cultured in regular petri dishes on day 5, respectively. In sum, the HGF/heparin-DLM films were effective in hepatocyte culturing and repairing D-galactosamine–induced hepatocyte damage. Thus, they have potential for future clinical applications. ? 2022 |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85123692840&doi=10.1016%2fj.bej.2022.108354&partnerID=40&md5=12ed80bac2d3503fb0b4bee34a2bb139 https://scholars.lib.ntu.edu.tw/handle/123456789/605955 |
ISSN: | 1369703X | DOI: | 10.1016/j.bej.2022.108354 |
顯示於: | 生物機電工程學系 |
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