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使用干细胞和类器官模型研究代谢性疾病和药物反应。

Modelling metabolic diseases and drug response using stem cells and organoids.

机构信息

Department of Basic Research, Guangzhou Laboratory, Guangdong, China.

Institute for Diabetes, Obesity, and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

出版信息

Nat Rev Endocrinol. 2022 Dec;18(12):744-759. doi: 10.1038/s41574-022-00733-z. Epub 2022 Sep 7.

Abstract

Metabolic diseases, including obesity, diabetes mellitus and cardiovascular disease, are a major threat to health in the modern world, but efforts to understand the underlying mechanisms and develop rational treatments are limited by the lack of appropriate human model systems. Notably, advances in stem cell and organoid technology allow the generation of cellular models that replicate the histological, molecular and physiological properties of human organs. Combined with marked improvements in gene editing tools, human stem cells and organoids provide unprecedented systems for studying mechanisms of metabolic diseases. Here, we review progress made over the past decade in the generation and use of stem cell-derived metabolic cell types and organoids in metabolic disease research, especially obesity and liver diseases. In particular, we discuss the limitations of animal models and the advantages of stem cells and organoids, including their application to metabolic diseases. We also discuss mechanisms of drug action, understanding the efficacy and toxicity of existing therapies, screening for new treatments and pursuing personalized therapies. We highlight the potential of combining stem cell-derived organoids with gene editing and functional genomics to revolutionize the approach to finding treatments for metabolic diseases.

摘要

代谢性疾病,包括肥胖、糖尿病和心血管疾病,是现代社会健康的主要威胁,但由于缺乏合适的人类模型系统,人们对这些疾病的潜在机制和合理治疗方法的理解仍有限。值得注意的是,干细胞和类器官技术的进步使人们能够生成能够复制人类器官组织学、分子和生理学特性的细胞模型。结合基因编辑工具的显著改进,人类干细胞和类器官为研究代谢性疾病的机制提供了前所未有的系统。在这里,我们回顾了过去十年中在代谢性疾病研究中利用干细胞衍生的代谢细胞类型和类器官取得的进展,特别是在肥胖和肝脏疾病方面的进展。特别地,我们讨论了动物模型的局限性和干细胞和类器官的优势,包括它们在代谢性疾病中的应用。我们还讨论了药物作用的机制,了解现有治疗方法的疗效和毒性,筛选新的治疗方法以及追求个性化治疗。我们强调了将干细胞衍生的类器官与基因编辑和功能基因组学相结合,为寻找代谢性疾病治疗方法带来革命性变化的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd1/9449917/6f3231f6cd12/41574_2022_733_Fig1_HTML.jpg

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