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本文引用的文献

1
Single cell transcriptomics identifies a signaling network coordinating endoderm and mesoderm diversification during foregut organogenesis.单细胞转录组学鉴定出一个在前肠器官发生过程中协调内胚层和中胚层分化的信号网络。
Nat Commun. 2020 Aug 27;11(1):4158. doi: 10.1038/s41467-020-17968-x.
2
Mechano-modulatory synthetic niches for liver organoid derivation.用于肝类器官衍生的机械调节合成小生境
Nat Commun. 2020 Jul 10;11(1):3416. doi: 10.1038/s41467-020-17161-0.
3
A Human Pluripotent Stem Cell-based Platform to Study SARS-CoV-2 Tropism and Model Virus Infection in Human Cells and Organoids.基于人多能干细胞的平台,用于研究 SARS-CoV-2 嗜性和人类细胞及类器官中的病毒感染模型。
Cell Stem Cell. 2020 Jul 2;27(1):125-136.e7. doi: 10.1016/j.stem.2020.06.015. Epub 2020 Jun 19.
4
Human Pluripotent Stem Cell-Derived Organoids as Models of Liver Disease.人多能干细胞衍生类器官作为肝脏疾病模型。
Gastroenterology. 2020 Oct;159(4):1471-1486.e12. doi: 10.1053/j.gastro.2020.06.010. Epub 2020 Jun 15.
5
3D culture of functional human iPSC-derived hepatocytes using a core-shell microfiber.使用核壳微纤维进行功能性人诱导多能干细胞源性肝细胞的 3D 培养
PLoS One. 2020 Jun 11;15(6):e0234441. doi: 10.1371/journal.pone.0234441. eCollection 2020.
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Assembly and Function of a Bioengineered Human Liver for Transplantation Generated Solely from Induced Pluripotent Stem Cells.生物工程化人肝用于移植的组装和功能,其细胞完全来源于诱导多能干细胞。
Cell Rep. 2020 Jun 2;31(9):107711. doi: 10.1016/j.celrep.2020.107711.
7
Use of 3D Human Liver Organoids to Predict Drug-Induced Phospholipidosis.使用 3D 人肝类器官预测药物诱导的磷脂沉积症。
Int J Mol Sci. 2020 Apr 23;21(8):2982. doi: 10.3390/ijms21082982.
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Long-Term Expansion of Functional Human Pluripotent Stem Cell-Derived Hepatic Organoids.功能性人多能干细胞来源的肝类器官的长期扩增
Int J Stem Cells. 2020 Jul 30;13(2):279-286. doi: 10.15283/ijsc20060.
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Multi-lineage Human iPSC-Derived Platforms for Disease Modeling and Drug Discovery.多谱系人诱导多能干细胞(iPSC)衍生平台用于疾病建模和药物发现。
Cell Stem Cell. 2020 Mar 5;26(3):309-329. doi: 10.1016/j.stem.2020.02.011.
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Cellulose Nanofibril Hydrogel Promotes Hepatic Differentiation of Human Liver Organoids.纤维素纳米原纤维水凝胶促进人肝脏类器官的肝分化。
Adv Healthc Mater. 2020 Mar;9(6):e1901658. doi: 10.1002/adhm.201901658. Epub 2020 Feb 23.

人源肝模型系统(体外)。

Human liver model systems in a dish.

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, USA.

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

出版信息

Dev Growth Differ. 2021 Jan;63(1):47-58. doi: 10.1111/dgd.12708. Epub 2021 Feb 2.

DOI:10.1111/dgd.12708
PMID:33423319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7940568/
Abstract

The human adult liver has a multi-cellular structure consisting of large lobes subdivided into lobules containing portal triads and hepatic cords lined by specialized blood vessels. Vital hepatic functions include filtering blood, metabolizing drugs, and production of bile and blood plasma proteins like albumin, among many other functions, which are generally dependent on the location or zone in which the hepatocyte resides in the liver. Due to the liver's intricate structure, there are many challenges to design differentiation protocols to generate more mature functional hepatocytes from human stem cells and maintain the long-term viability and functionality of primary hepatocytes. To this end, recent advancements in three-dimensional (3D) stem cell culture have accelerated the generation of a human miniature liver system, also known as liver organoids, with polarized epithelial cells, supportive cell types and extra-cellular matrix deposition by translating knowledge gained in studies of animal organogenesis and regeneration. To facilitate the efforts to study human development and disease using in vitro hepatic models, a thorough understanding of state-of-art protocols and underlying rationales is essential. Here, we review rapidly evolving 3D liver models, mainly focusing on organoid models differentiated from human cells.

摘要

成人肝脏具有多细胞结构,由大的叶组成,进一步分为含有门三联体的小叶,小叶由专门的血管组成。肝脏的重要功能包括过滤血液、代谢药物以及产生胆汁和血浆蛋白(如白蛋白)等,这些功能通常取决于肝细胞在肝脏中的位置或区域。由于肝脏结构复杂,因此设计从人类干细胞中生成更成熟的功能性肝细胞的分化方案以及维持原代肝细胞的长期存活和功能存在许多挑战。为此,最近在三维(3D)干细胞培养方面的进展加速了人类微型肝脏系统的生成,也称为肝类器官,具有极化的上皮细胞、支持细胞类型和细胞外基质沉积,这是通过将动物器官发生和再生研究中获得的知识转化而来的。为了促进使用体外肝脏模型研究人类发育和疾病的工作,深入了解最先进的方案和基本原理至关重要。在这里,我们综述了快速发展的 3D 肝脏模型,主要侧重于从人类细胞分化而来的类器官模型。