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基于PSC的肝纤维化治疗的当前进展

The Current Proceedings of PSC-Based Liver Fibrosis Therapy.

作者信息

Ma Li, Wu Qiang, Tam Paul Kwong-Hang

机构信息

The State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Taipa, China.

Faculty of Medicine, Macau University of Science and Technology, Taipa, China.

出版信息

Stem Cell Rev Rep. 2023 Oct;19(7):2155-2165. doi: 10.1007/s12015-023-10592-4. Epub 2023 Jul 25.

DOI:10.1007/s12015-023-10592-4
PMID:37490204
Abstract

Liver fibrosis was initially considered to be an irreversible process which will eventually lead to the occurrence of liver cancer. So far there has been no effective therapeutic approach to treat liver fibrosis although scientists have put tremendous efforts into the underlying mechanisms of this disease. Therefore, in-depth research on novel and safe treatments of liver fibrosis is of great significance to human health. Pluripotent stem cells (PSCs) play important roles in the study of liver fibrosis due to their unique features in self-renewal ability, pluripotency, and paracrine function. This article mainly reviews the applications of PSCs in the study of liver fibrosis in recent years. We discuss the role of PSC-derived liver organoids in the study of liver fibrosis, and the latest research advances on the differentiation of PSCs into hepatocytes or macrophages. We also highlight the importance of exosomes of PSCs for the treatment of liver fibrosis.

摘要

肝纤维化最初被认为是一个不可逆的过程,最终会导致肝癌的发生。尽管科学家们在该疾病的潜在机制方面付出了巨大努力,但迄今为止,尚无有效的治疗方法来治疗肝纤维化。因此,深入研究新型且安全的肝纤维化治疗方法对人类健康具有重要意义。多能干细胞(PSCs)因其在自我更新能力、多能性和旁分泌功能方面的独特特性,在肝纤维化研究中发挥着重要作用。本文主要综述了近年来多能干细胞在肝纤维化研究中的应用。我们讨论了多能干细胞来源的肝类器官在肝纤维化研究中的作用,以及多能干细胞向肝细胞或巨噬细胞分化的最新研究进展。我们还强调了多能干细胞外泌体在治疗肝纤维化中的重要性。

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The Current Proceedings of PSC-Based Liver Fibrosis Therapy.基于PSC的肝纤维化治疗的当前进展
Stem Cell Rev Rep. 2023 Oct;19(7):2155-2165. doi: 10.1007/s12015-023-10592-4. Epub 2023 Jul 25.
2
Generation of expandable human pluripotent stem cell-derived hepatocyte-like liver organoids.扩增型人多能干细胞来源的肝样类器官的生成。
J Hepatol. 2019 Nov;71(5):970-985. doi: 10.1016/j.jhep.2019.06.030. Epub 2019 Jul 9.
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Modeling human liver organ development and diseases with pluripotent stem cell-derived organoids.利用多能干细胞来源的类器官模拟人类肝脏器官发育和疾病
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引用本文的文献

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Biliary fibrosis is an important but neglected pathological feature in hepatobiliary disorders: from molecular mechanisms to clinical implications.胆汁纤维化是肝胆疾病中一个重要但被忽视的病理特征:从分子机制到临床意义。
Med Rev (2021). 2024 Jul 1;4(4):326-365. doi: 10.1515/mr-2024-0029. eCollection 2024 Aug.

本文引用的文献

1
Modeling drug-induced liver injury and screening for anti-hepatofibrotic compounds using human PSC-derived organoids.利用人PSC来源的类器官模拟药物性肝损伤并筛选抗肝纤维化化合物。
Cell Regen. 2023 Mar 3;12(1):6. doi: 10.1186/s13619-022-00148-1.
2
Generation of functionally competent hepatic stellate cells from human stem cells to model liver fibrosis in vitro.从人干细胞生成功能成熟的肝星状细胞以体外模拟肝纤维化。
Stem Cell Reports. 2022 Nov 8;17(11):2531-2547. doi: 10.1016/j.stemcr.2022.09.010. Epub 2022 Oct 20.
3
CD133-Src-TAZ signaling stimulates ductal fibrosis following DDC diet-induced liver injury.
CD133-Src-TAZ 信号通路激活促进 DDC 饮食诱导的肝损伤后的胆管纤维化。
J Cell Physiol. 2022 Dec;237(12):4504-4516. doi: 10.1002/jcp.30899. Epub 2022 Oct 17.
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Modelling fatty liver disease with mouse liver-derived multicellular spheroids.利用小鼠肝源多细胞球体模拟脂肪肝疾病。
Biomaterials. 2022 Nov;290:121817. doi: 10.1016/j.biomaterials.2022.121817. Epub 2022 Sep 28.
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Human organoids in basic research and clinical applications.人类器官类器官在基础研究和临床应用中的应用。
Signal Transduct Target Ther. 2022 May 24;7(1):168. doi: 10.1038/s41392-022-01024-9.
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Differential effects of macrophage subtypes on SARS-CoV-2 infection in a human pluripotent stem cell-derived model.巨噬细胞亚型对人多能干细胞衍生模型中 SARS-CoV-2 感染的差异影响。
Nat Commun. 2022 Apr 19;13(1):2028. doi: 10.1038/s41467-022-29731-5.
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Therapeutically harnessing extracellular vesicles.治疗性利用细胞外囊泡。
Nat Rev Drug Discov. 2022 May;21(5):379-399. doi: 10.1038/s41573-022-00410-w. Epub 2022 Mar 2.
8
Multiparameter magnetic resonance imaging of liver fibrosis in a bile duct ligation mouse model.多参数磁共振成像在胆管结扎小鼠模型中的肝纤维化研究。
World J Gastroenterol. 2021 Dec 21;27(47):8156-8165. doi: 10.3748/wjg.v27.i47.8156.
9
3D hESC exosomes enriched with miR-6766-3p ameliorates liver fibrosis by attenuating activated stellate cells through targeting the TGFβRII-SMADS pathway.富含 miR-6766-3p 的 3D hESC 外泌体通过靶向 TGFβRII-SMADS 通路减弱激活的星状细胞来改善肝纤维化。
J Nanobiotechnology. 2021 Dec 20;19(1):437. doi: 10.1186/s12951-021-01138-2.
10
Hepatic fibrosis 2022: Unmet needs and a blueprint for the future.2022 年肝脏纤维化:未满足的需求和未来蓝图。
Hepatology. 2022 Feb;75(2):473-488. doi: 10.1002/hep.32285. Epub 2022 Jan 11.