Suppr超能文献

对单个胆管细胞衍生类器官的 RNA 测序揭示了类器官间的高度变异性。

RNA-sequencing of single cholangiocyte-derived organoids reveals high organoid-to organoid variability.

机构信息

Max Planck Research Group "Chromatin and Ageing," Max Planck Institute for Biology of Ageing, Cologne, Germany.

Cologne Excellence Cluster on Cellular Stress Responses in Aging-associated Diseases (CECAD), Cologne, Germany.

出版信息

Life Sci Alliance. 2022 Aug 1;5(12):e202101340. doi: 10.26508/lsa.202101340.

Abstract

Over the last decades, organoids have been established from most of the tissue-resident stem and iPS cells. They hold great promise for our understanding of mammalian organ development, but also for the study of disease or even personalised medicine. In recent years, several reports hinted at intraculture organoid variability, but a systematic analysis of such heterogeneity has not been performed before. Here, we used RNA-seq of individual intrahepatic cholangiocyte organoids to address this question. We find that batch-to-batch variation is very low, whereas passage number has a profound impact on gene expression profiles. On the other hand, there is organoid-to-organoid variability within a culture. Using differential gene expression, we did not identify specific pathways that drive this variability, pointing towards possible effects of the microenvironment within the culture condition. Taken together, our study provides a framework for organoid researchers to properly consider experimental design.

摘要

在过去的几十年中,已经从大多数组织驻留的干细胞和 iPS 细胞中建立了类器官。它们为我们理解哺乳动物器官发育,甚至为疾病研究甚至个性化医学提供了巨大的希望。近年来,有几项报道暗示了类器官培养中的内在变异性,但之前尚未对这种异质性进行系统分析。在这里,我们使用单个肝内胆管细胞类器官的 RNA-seq 来解决这个问题。我们发现,批次间的变化非常低,而传代数对基因表达谱有深远的影响。另一方面,在同一培养物中存在类器官间的变异性。通过差异基因表达,我们没有鉴定出驱动这种变异性的特定途径,这表明培养条件中的微环境可能有影响。总之,我们的研究为类器官研究人员提供了一个框架,以正确考虑实验设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6adc/9348635/dd1c96cd2eeb/LSA-2021-01340_Fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验