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3D hepatic organoid production from human pluripotent stem cells.
Jin, Zhe-Long; Xu, KangHe; Kim, Jonghun; Guo, Hao; Yao, Xuerui; Xu, Yong-Nan; Li, Ying-Hua; Ryu, DongHee; Kim, Kee-Pyo; Hong, Kwonho; Kim, Yong-June; Wang, Lin; Cao, Qilong; Kim, Kyun-Hwan; Kim, Nam-Hyung; Han, Dong Wook.
Affiliation
  • Jin ZL; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, China; International Healthcare Innovation Institute (Jiangmen), Jianghai, Jiangmen, Guangdong Province, China; Research and Development Department, Qin
  • Xu K; Department of Surgery, College of Medicine, Chungbuk National University, Cheongju, 28864, Republic of Korea.
  • Kim J; Department of Genetics, Yale Stem Cell Center, Yale Child Study Center, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Guo H; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, China; International Healthcare Innovation Institute (Jiangmen), Jianghai, Jiangmen, Guangdong Province, China; Research and Development Department, Qin
  • Yao X; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, China; International Healthcare Innovation Institute (Jiangmen), Jianghai, Jiangmen, Guangdong Province, China; Research and Development Department, Qin
  • Xu YN; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, China.
  • Li YH; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, China.
  • Ryu D; Department of Surgery, College of Medicine, Chungbuk National University, Cheongju, 28864, Republic of Korea; Department of Surgery, Chungbuk National University Hospital, Cheongju, 28864, Republic of Korea.
  • Kim KP; Department of Life Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
  • Hong K; Department of Stem Cell and Regenerative Biotechnology and Humanized Pig Center (SRC), Konkuk University, Seoul, 05029, Republic of Korea.
  • Kim YJ; Department of Urology, College of Medicine, Chungbuk National University, Cheongju, 28864, Republic of Korea; Department of Urology, Chungbuk National University Hospital, Cheongju, 28864, Republic of Korea.
  • Wang L; Research and Development Department, Qingdao Haier Biotech Co. Ltd, Qingdao, China.
  • Cao Q; Research and Development Department, Qingdao Haier Biotech Co. Ltd, Qingdao, China.
  • Kim KH; Department of Precision Medicine, School of Medicine, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Kim NH; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, China; Research and Development Department, Qingdao Haier Biotech Co. Ltd, Qingdao, China; Laboratory of Stem Cells and Organoids, OrganFactory Co., Ltd
  • Han DW; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, China; Research and Development Department, Qingdao Haier Biotech Co. Ltd, Qingdao, China; Laboratory of Stem Cells and Organoids, OrganFactory Co., Ltd
Differentiation ; 135: 100742, 2024.
Article in En | MEDLINE | ID: mdl-38104501
ABSTRACT
Hepatic organoids might provide a golden opportunity for realizing precision medicine in various hepatic diseases. Previously described hepatic organoid protocols from pluripotent stem cells rely on complicated multiple differentiation steps consisting of both 2D and 3D differentiation procedures. Therefore, the spontaneous formation of hepatic organoids from 2D monolayer culture is associated with a low-throughput production, which might hinder the standardization of hepatic organoid production and hamper the translation of this technology to the clinical or industrial setting. Here we describe the stepwise and fully 3D production of hepatic organoids from human pluripotent stem cells. We optimized every differentiation step by screening for optimal concentrations and timing of differentiation signals in each differentiation step. Hepatic organoids are stably expandable without losing their hepatic functionality. Moreover, upon treatment of drugs with known hepatotoxicity, we found hepatic organoids are more sensitive to drug-induced hepatotoxicity compared with 2D hepatocytes differentiated from PSCs, making them highly suitable for in vitro toxicity screening of drug candidates. The standardized fully 3D protocol described in the current study for producing functional hepatic organoids might serve as a novel platform for the industrial and clinical translation of hepatic organoid technology.
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Full text: 1 Database: MEDLINE Main subject: Pluripotent Stem Cells / Induced Pluripotent Stem Cells / Chemical and Drug Induced Liver Injury Limits: Humans Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Pluripotent Stem Cells / Induced Pluripotent Stem Cells / Chemical and Drug Induced Liver Injury Limits: Humans Language: En Year: 2024 Type: Article