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时空成像与分析小鼠和人肝原基形态发生。

Spatiotemporal imaging and analysis of mouse and human liver bud morphogenesis.

机构信息

Department of Chemical and Biological Engineering, University at Buffalo (State University of New York), Buffalo, New York, USA.

Department of Biological Sciences, College of Arts and Sciences, University at Buffalo (State University of New York), Buffalo, New York, USA.

出版信息

Dev Dyn. 2022 Apr;251(4):662-686. doi: 10.1002/dvdy.429. Epub 2021 Nov 6.

Abstract

BACKGROUND

The process of liver organogenesis has served as a paradigm for organ formation. However, there remains a lack of understanding regarding early mouse and human liver bud morphogenesis and early liver volumetric growth. Elucidating dynamic changes in liver volumes is critical for understanding organ development, implementing toxicological studies, and for modeling hPSC-derived liver organoid growth. New visualization, analysis, and experimental techniques are desperately needed.

RESULTS

Here, we combine observational data with digital resources, new 3D imaging approaches, retrospective analysis of liver volume data, mathematical modeling, and experiments with hPSC-derived liver organoids. Mouse and human liver organogenesis, characterized by exponential growth, demonstrate distinct spatial features and growth curves over time, which we mathematically modeled using Gompertz models. Visualization of liver-epithelial and septum transversum mesenchyme (STM) interactions suggests extended interactions, which together with new spatial features may be responsible for extensive exponential growth. These STM interactions are modeled with a novel in vitro human pluripotent stem cell (hPSC)-derived hepatic organoid system that exhibits cell migration.

CONCLUSIONS

Our methods enhance our understanding of liver organogenesis, with new 3D visualization, analysis, mathematical modeling, and in vitro models with hPSCs. Our approach highlights mouse and human differences and provides potential hypothesis for further investigation in vitro and in vivo.

摘要

背景

肝脏器官发生过程一直是器官形成的典范。然而,对于早期小鼠和人类肝芽形态发生和早期肝体积生长,我们仍缺乏了解。阐明肝体积的动态变化对于理解器官发育、实施毒理学研究以及对 hPSC 衍生的肝类器官生长进行建模至关重要。迫切需要新的可视化、分析和实验技术。

结果

在这里,我们将观察数据与数字资源、新的 3D 成像方法、肝体积数据的回顾性分析、数学建模以及 hPSC 衍生的肝类器官实验相结合。以指数生长为特征的小鼠和人类肝脏发生显示出随时间推移具有独特的空间特征和生长曲线,我们使用 Gompertz 模型对其进行了数学建模。可视化肝上皮和横膈膜间充质 (STM) 之间的相互作用表明存在扩展的相互作用,这些相互作用以及新的空间特征可能是广泛指数生长的原因。这些 STM 相互作用通过新型体外人多能干细胞 (hPSC) 衍生的肝类器官系统进行建模,该系统表现出细胞迁移。

结论

我们的方法通过新的 3D 可视化、分析、数学建模以及 hPSC 的体外模型,增强了我们对肝脏发生的理解。我们的方法突出了小鼠和人类之间的差异,并为进一步的体外和体内研究提供了潜在的假说。

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