Terry Fox Laboratory, BC Cancer, Vancouver, BC, Canada.
Cell and Developmental Biology Program, University of British Columbia, Vancouver, BC, Canada.
Nat Rev Gastroenterol Hepatol. 2023 Sep;20(9):561-581. doi: 10.1038/s41575-023-00775-2. Epub 2023 May 19.
The metabolic, digestive and homeostatic roles of the liver are dependent on proper crosstalk and organization of hepatic cell lineages. These hepatic cell lineages are derived from their respective progenitors early in organogenesis in a spatiotemporally controlled manner, contributing to the liver's specialized and diverse microarchitecture. Advances in genomics, lineage tracing and microscopy have led to seminal discoveries in the past decade that have elucidated liver cell lineage hierarchies. In particular, single-cell genomics has enabled researchers to explore diversity within the liver, especially early in development when the application of bulk genomics was previously constrained due to the organ's small scale, resulting in low cell numbers. These discoveries have substantially advanced our understanding of cell differentiation trajectories, cell fate decisions, cell lineage plasticity and the signalling microenvironment underlying the formation of the liver. In addition, they have provided insights into the pathogenesis of liver disease and cancer, in which developmental processes participate in disease emergence and regeneration. Future work will focus on the translation of this knowledge to optimize in vitro models of liver development and fine-tune regenerative medicine strategies to treat liver disease. In this Review, we discuss the emergence of hepatic parenchymal and non-parenchymal cells, advances that have been made in in vitro modelling of liver development and draw parallels between developmental and pathological processes.
肝脏的代谢、消化和稳态作用取决于肝谱系细胞的正确串扰和组织。这些肝谱系细胞由其各自的祖细胞在器官发生早期以时空控制的方式产生,有助于肝脏的特化和多样化的微观结构。基因组学、谱系追踪和显微镜技术的进步在过去十年中取得了开创性的发现,阐明了肝谱系细胞的层次结构。特别是,单细胞基因组学使研究人员能够探索肝脏内的多样性,特别是在发育早期,由于器官规模较小,批量基因组学的应用以前受到限制,导致细胞数量较少。这些发现大大提高了我们对细胞分化轨迹、细胞命运决定、细胞谱系可塑性以及肝脏形成的信号微环境的理解。此外,它们还深入了解了肝脏疾病和癌症的发病机制,其中发育过程参与了疾病的发生和再生。未来的工作将集中在将这些知识转化为优化肝脏发育的体外模型,并微调再生医学策略以治疗肝脏疾病。在这篇综述中,我们讨论了肝实质和非实质细胞的出现,以及在肝脏发育的体外模型方面取得的进展,并在发育和病理过程之间进行了类比。