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功能性肝胆类器官概括了肝脏发育过程,并揭示了肝胆细胞命运决定的关键驱动因素。

Functional hepatobiliary organoids recapitulate liver development and reveal essential drivers of hepatobiliary cell fate determination.

作者信息

He Juan, Cui Haoyue, Shi Xiaohan, Jin Qiqi, Han Ximeng, Han Tiantian, Peng Jiayin, Guo Shiwei, Zhang Lei, Zhao Yun, Zhou Bin, Chen Luonan, Chen Lei, Arial Zeng Yi, Wang Hongyang, Jin Gang, Gao Dong

机构信息

State Key Laboratory of Cell Biology, Shanghai Key Laboratory of Molecular Andrology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai 200031, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Life Med. 2022 Dec 7;1(3):345-358. doi: 10.1093/lifemedi/lnac055. eCollection 2022 Dec.

Abstract

During liver development, hepatocytes, and cholangiocytes are concurrently differentiated from common liver progenitor cells and are assembled into hepatobiliary architecture to perform proper hepatic function. However, the generation of functional hepatobiliary architecture from hepatocytes is still challenging, and the exact molecular drivers of hepatobiliary cell lineage determination is largely unknown. In this study, functional hepatobiliary organoids (HBOs) are generated from hepatocytes. These HBOs contain a bile duct network surrounded by mature hepatocytes and stably maintain hepatic characteristics and function and upon transplantation . Morphological transition and expression profile of hepatocyte-derived organoids recapitulate the process of liver development. Gene regulation landscape of hepatocyte-derived organoids reveal that and promote the cell fate commitment of liver progenitors to functional cholangiocytes and hepatocytes, respectively. Liver cell fate determination is reversed by inhibiting or increasing Ddit3 expression both and upon transplantation . Collectively, hepatocyte-derived HBOs reveal the essential transcription drivers of liver hepatobiliary cell lineage determination and represent powerful models for liver development and regeneration.

摘要

在肝脏发育过程中,肝细胞和胆管细胞同时从共同的肝脏祖细胞分化而来,并组装成肝胆结构以执行正常的肝脏功能。然而,从肝细胞生成功能性肝胆结构仍然具有挑战性,并且肝胆细胞谱系确定的确切分子驱动因素在很大程度上尚不清楚。在本研究中,从肝细胞生成了功能性肝胆类器官(HBO)。这些HBO包含由成熟肝细胞包围的胆管网络,并在移植后稳定地维持肝脏特征和功能。肝细胞衍生类器官的形态转变和表达谱概括了肝脏发育过程。肝细胞衍生类器官的基因调控图谱显示,[此处原文缺失两个关键基因名称]分别促进肝脏祖细胞向功能性胆管细胞和肝细胞的细胞命运定向。通过抑制[此处原文缺失关键基因名称]或增加Ddit3表达,无论是在体外还是移植后,肝细胞命运的确定都会发生逆转。总体而言,肝细胞衍生的HBO揭示了肝脏肝胆细胞谱系确定的关键转录驱动因素,并代表了肝脏发育和再生的强大模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3db0/11749142/6da5e1daec93/lnac055_fig1.jpg

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