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肝类器官从青春期发育至成熟。

Hepatic organoids move from adolescence to maturity.

作者信息

Guan Yuan, Peltz Gary

机构信息

Department of Anesthesia, Pain and Perioperative Medicine, Stanford University School of Medicine, Stanford, California, USA.

出版信息

Liver Int. 2024 Jun;44(6):1290-1297. doi: 10.1111/liv.15893. Epub 2024 Mar 7.

DOI:10.1111/liv.15893
PMID:38451053
Abstract

Since organoids were developed 15 years ago, they are now in their adolescence as a research tool. The ability to generate 'tissue in a dish' has created enormous opportunities for biomedical research. We examine the contributions that hepatic organoids have made to three areas of liver research: as a source of cells and tissue for basic research, for drug discovery and drug safety testing, and for understanding disease pathobiology. We discuss the features that enable hepatic organoids to provide useful models for human liver diseases and identify four types of advances that will enable them to become a mature (i.e., adult) research tool over the next 5 years. During this period, advances in single-cell RNA sequencing and CRISPR technologies coupled with improved hepatic organoid methodology, which enables them to have a wider range of cell types that are present in liver and to be grown in microwells, will generate discoveries that will dramatically advance our understanding of liver development and the pathogenesis of liver diseases. It will generate also new approaches for treating liver fibrosis, which remains a major public health problem with few treatment options.

摘要

自类器官在15年前被开发以来,如今作为一种研究工具,它们正处于“青春期”。生成“培养皿中的组织”的能力为生物医学研究创造了巨大机遇。我们研究了肝类器官在肝脏研究的三个领域所做出的贡献:作为基础研究的细胞和组织来源、用于药物发现和药物安全性测试,以及用于理解疾病病理生物学。我们讨论了使肝类器官能够为人类肝脏疾病提供有用模型的特征,并确定了四种进展,这些进展将使它们在未来5年内成为一种成熟(即成年)的研究工具。在此期间,单细胞RNA测序和CRISPR技术的进展,再加上改进的肝类器官方法,使它们能够拥有更广泛的肝脏中存在的细胞类型,并能在微孔中生长,这将带来一些发现,极大地推动我们对肝脏发育和肝脏疾病发病机制的理解。这也将产生治疗肝纤维化的新方法,肝纤维化仍然是一个主要的公共卫生问题,治疗选择很少。

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