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考虑使用分离的细胞系统来理解心脏代谢和生物学。

Considerations for using isolated cell systems to understand cardiac metabolism and biology.

机构信息

Department of Medicine, Division of Environmental Medicine, Christina Lee Brown Envirome Institute, Diabetes and Obesity Center, University of Louisville, Louisville, KY, USA.

Department of Medicine, Division of Environmental Medicine, Christina Lee Brown Envirome Institute, Diabetes and Obesity Center, University of Louisville, Louisville, KY, USA.

出版信息

J Mol Cell Cardiol. 2021 Apr;153:26-41. doi: 10.1016/j.yjmcc.2020.12.007. Epub 2020 Dec 21.

Abstract

Changes in myocardial metabolic activity are fundamentally linked to cardiac health and remodeling. Primary cardiomyocytes, induced pluripotent stem cell-derived cardiomyocytes, and transformed cardiomyocyte cell lines are common models used to understand how (patho)physiological conditions or stimuli contribute to changes in cardiac metabolism. These cell models are helpful also for defining metabolic mechanisms of cardiac dysfunction and remodeling. Although technical advances have improved our capacity to measure cardiomyocyte metabolism, there is often heterogeneity in metabolic assay protocols and cell models, which could hinder data interpretation and discernment of the mechanisms of cardiac (patho)physiology. In this review, we discuss considerations for integrating cardiomyocyte cell models with techniques that have become relatively common in the field, such as respirometry and extracellular flux analysis. Furthermore, we provide overviews of metabolic assays that complement XF analyses and that provide information on not only catabolic pathway activity, but biosynthetic pathway activity and redox status as well. Cultivating a more widespread understanding of the advantages and limitations of metabolic measurements in cardiomyocyte cell models will continue to be essential for the development of coherent metabolic mechanisms of cardiac health and pathophysiology.

摘要

心肌代谢活性的变化与心脏健康和重构密切相关。原代心肌细胞、诱导多能干细胞衍生的心肌细胞和转化的心肌细胞系是常用的模型,用于了解(病理)生理条件或刺激如何导致心脏代谢的变化。这些细胞模型对于定义心脏功能障碍和重构的代谢机制也很有帮助。尽管技术进步提高了我们测量心肌细胞代谢的能力,但代谢测定方案和细胞模型往往存在异质性,这可能会阻碍数据解释和辨别心脏(病理)生理学的机制。在这篇综述中,我们讨论了将心肌细胞模型与该领域中相对常见的技术(如呼吸测量法和细胞外通量分析)相结合的注意事项。此外,我们还概述了补充 XF 分析的代谢测定方法,这些方法不仅提供了分解代谢途径活性的信息,还提供了合成代谢途径活性和氧化还原状态的信息。培养对心肌细胞模型中代谢测量的优势和局限性的更广泛理解,对于心脏健康和病理生理学的一致代谢机制的发展将继续至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae11/8026511/4e25d213d549/nihms-1657982-f0001.jpg

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