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Curr Opin Genet Dev. 2022 Aug;75:101925. doi: 10.1016/j.gde.2022.101925. Epub 2022 Jun 11.
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本文引用的文献

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Quantitative lineage analysis identifies a hepato-pancreato-biliary progenitor niche.定量谱系分析确定了肝胆胰胆管祖细胞龛位。
Nature. 2021 Sep;597(7874):87-91. doi: 10.1038/s41586-021-03844-1. Epub 2021 Aug 25.
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Organogenesis in vitro.体外器官发生。
Curr Opin Cell Biol. 2021 Dec;73:84-91. doi: 10.1016/j.ceb.2021.06.007. Epub 2021 Aug 2.
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Integrating Spatial Transcriptomics and Single-Cell RNA-seq Reveals the Gene Expression Profling of the Human Embryonic Liver.整合空间转录组学和单细胞RNA测序揭示人类胚胎肝脏的基因表达谱。
Front Cell Dev Biol. 2021 May 20;9:652408. doi: 10.3389/fcell.2021.652408. eCollection 2021.
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Establishing a 3D In Vitro Hepatic Model Mimicking Physiologically Relevant to In Vivo State.建立一个模拟体内生理状态的 3D 体外肝脏模型。
Cells. 2021 May 20;10(5):1268. doi: 10.3390/cells10051268.
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Tissue-Specific Microparticles Improve Organoid Microenvironment for Efficient Maturation of Pluripotent Stem-Cell-Derived Hepatocytes.组织特异性微粒改善类器官微环境,以提高多能干细胞来源的肝细胞的成熟效率。
Cells. 2021 May 21;10(6):1274. doi: 10.3390/cells10061274.
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A single cell gene expression atlas of 28 human livers.28个人类肝脏的单细胞基因表达图谱
J Hepatol. 2021 Jul;75(1):219-220. doi: 10.1016/j.jhep.2021.03.005. Epub 2021 May 18.
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A computer-guided design tool to increase the efficiency of cellular conversions.一种用于提高细胞转化效率的计算机辅助设计工具。
Nat Commun. 2021 Mar 12;12(1):1659. doi: 10.1038/s41467-021-21801-4.
8
Cholangiocyte organoids can repair bile ducts after transplantation in the human liver.胆管细胞类器官可在人肝移植后修复胆管。
Science. 2021 Feb 19;371(6531):839-846. doi: 10.1126/science.aaz6964.
9
Engineering human hepato-biliary-pancreatic organoids from pluripotent stem cells.从多能干细胞中工程化人类肝胆胰腺类器官。
Nat Protoc. 2021 Feb;16(2):919-936. doi: 10.1038/s41596-020-00441-w. Epub 2021 Jan 11.
10
Gene Regulatory Network Analysis and Engineering Directs Development and Vascularization of Multilineage Human Liver Organoids.基因调控网络分析和工程指导多谱系人类肝类器官的发育和血管生成。
Cell Syst. 2021 Jan 20;12(1):41-55.e11. doi: 10.1016/j.cels.2020.11.002. Epub 2020 Dec 7.

肝脏的叙事工程。

Narrative engineering of the liver.

机构信息

Division of Gastroenterology, Hepatology & Nutrition, Developmental Biology, Center for Stem Cell and Organoid Medicine (CuSTOM), Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229-3039, USA.

Division of Gastroenterology, Hepatology & Nutrition, Developmental Biology, Center for Stem Cell and Organoid Medicine (CuSTOM), Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229-3039, USA; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA; Institute of Research, Tokyo Medical and Dental University (TMDU), Tokyo, Japan; Communication Design Center, Advanced Medical Research Center, Yokohama City University Graduate School of Medicine, Japan.

出版信息

Curr Opin Genet Dev. 2022 Aug;75:101925. doi: 10.1016/j.gde.2022.101925. Epub 2022 Jun 11.

DOI:10.1016/j.gde.2022.101925
PMID:35700688
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10118678/
Abstract

Liver organoids are primary or pluripotent stem cell-derived three-dimensional structures that recapitulate regenerative or ontogenetic processes in vitro towards biomedical applications including disease modelling and diagnostics, drug safety and efficacy prediction, and therapeutic use. The cellular composition and structural organization of liver organoids may vary depending on the goal at hand, and the key challenge in general is to direct their development in a rational and controlled fashion for gaining targeted maturity, reproducibility, and scalability. Such endeavor begins with a detailed understanding of the biological processes in space and time behind hepatogenesis, followed by precise translation of these narrative processes through a bioengineering approach. Here, we discuss advancements in liver organoid technology through the lens of 'narrative engineering' in an attempt to synergize evolving understanding around molecular and cellular landscape governing hepatogenesis with engineering-inspired approaches for organoidgenesis.

摘要

肝脏类器官是由原代或多能干细胞衍生而来的三维结构,可在体外重现再生或个体发生过程,用于包括疾病建模和诊断、药物安全性和疗效预测以及治疗用途在内的生物医学应用。肝脏类器官的细胞组成和结构组织可能因手头的目标而异,一般来说,关键挑战是通过合理和可控的方式指导其发育,以获得靶向成熟度、可重复性和可扩展性。这种努力始于详细了解肝发生背后的时空生物学过程,然后通过生物工程方法精确转化这些叙述过程。在这里,我们通过“叙事工程”的视角讨论肝脏类器官技术的进展,试图将围绕着调控肝发生的分子和细胞景观的不断发展的理解与受工程启发的类器官发生方法相结合。