The efficient generation of functional human hepatocytes from chemically induced pluripotent stem cells

Author:

Lv Yun1,Rao Ziyan23,Liu Lulu4,Jia Jun5,Wu Chenyang23ORCID,Xu Jun6,Du Yuanyuan1,Liu Yinan6,Liu Bei1,Shi Jihang7,Li Guangya8,Zhao Dongyu23ORCID,Deng Hongkui15ORCID

Affiliation:

1. School of Basic Medical Sciences, MOE Engineering Research Center of Regenerative Medicine, State Key Laboratory of Natural and Biomimetic Drugs Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking‐Tsinghua Center for Life Sciences, Peking University Beijing China

2. Department of Biomedical Informatics, School of Basic Medical Sciences Peking University Health Science Center Beijing China

3. State Key Laboratory of Vascular Homeostasis and Remodeling Peking University Beijing China

4. Peking University‐Tsinghua University‐National Institute of Biological Science Joint Graduate Program, Academy for Advanced Interdisciplinary Studies, Peking University Beijing China

5. Changping Laboratory Beijing China

6. Department of Cell Biology, School of Basic Medical Sciences Peking University Stem Cell Research Center, Peking University Health Science Center, Peking University Beijing China

7. Department of Hepatobiliary Surgery, First Medical Center of Chinese PLA General Hospital Beijing China

8. Ministry of Education (MOE) Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking‐Tsinghua Center for Life Sciences Peking University Beijing China

Abstract

AbstractDerivation of human hepatocytes from pluripotent stem cells in vitro has important applications including cell therapy and drug discovery. However, the differentiation of pluripotent stem cells into hepatocytes in vitro was not well recapitulated the development of liver. Here, we developed a differentiation protocol by mimicking the two‐stage development of hepatoblasts, which permits the efficient generation of hepatic progenitor cells from chemically induced pluripotent stem cells (hCiPSCs). Single‐cell RNA sequencing (scRNA‐seq) indicates the similarity between hepatoblasts differentiated in vitro and in vivo. Moreover, hCiPSC‐derived hepatic progenitor cells can further differentiate into hepatocytes that are similar to primary human hepatocytes with respect to gene expression and key hepatic functions. Our results demonstrate the feasibility of generating hepatic progenitor cells and hepatocytes from hCiPSCs with high efficiency and set the foundation for broad translational applications of hCiPSC‐derived hepatocytes.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cell Biology,General Medicine

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