Enhancing generation efficiency of liver organoids in a collagen scaffold using human chemically derived hepatic progenitors

Liver organoids have emerged as a powerful tool for studying liver biology and disease and for developing new therapies and regenerative medicine approaches. For organoid culture, Matrigel, a type of extracellular matrix, is the most commonly used material. However, Matrigel cannot be used for clini...

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Published in:Annals of hepato-biliary-pancreatic surgery Vol. 27; no. 4; pp. 342 - 349
Main Authors: Kim, Myounghoi, Kim, Yohan, Silva, Elsy Soraya Salas, Adisasmita, Michael, Kim, Kyeong Sik, Jung, Yun Kyung, Lee, Kyeong Geun, Shin, Ji Hyun, Choi, Dongho
Format: Journal Article
Language:English
Published: Korea (South) 한국간담췌외과학회 30-11-2023
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Summary:Liver organoids have emerged as a powerful tool for studying liver biology and disease and for developing new therapies and regenerative medicine approaches. For organoid culture, Matrigel, a type of extracellular matrix, is the most commonly used material. However, Matrigel cannot be used for clinical applications due to the presence of unknown proteins that can cause immune rejection, batch-to-batch variability, and angiogenesis. To obtain human primary hepatocytes (hPHs), we performed 2 steps collagenase liver perfusion protocol. We treated three small molecules cocktails (A83-01, CHIR99021, and HGF) for reprogramming the hPHs into human chemically derived hepatic progenitors (hCdHs) and used hCdHs to generate liver organoids. In this study, we report the generation of liver organoids in a collagen scaffold using hCdHs. In comparison with adult liver (or primary hepatocyte)-derived organoids with collagen scaffold (hALO_C), hCdH-derived organoids in a collagen scaffold (hCdHO_C) showed a 10-fold increase in organoid generation efficiency with higher expression of liver- or liver progenitor-specific markers. Moreover, we demonstrated that hCdHO_C could differentiate into hepatic organoids (hCdHO_C_DM), indicating the potential of these organoids as a platform for drug screening. Overall, our study highlights the potential of hCdHO_C as a tool for liver research and presents a new approach for generating liver organoids using hCdHs with a collagen scaffold.
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content type line 23
ISSN:2508-5778
2508-5859
DOI:10.14701/ahbps.23-052