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心脏 3D 纳米动力学的电子显微镜观察:形态、功能与未来。

Electron microscopy of cardiac 3D nanodynamics: form, function, future.

机构信息

Institute for Experimental Cardiovascular Medicine, University Heart Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Faculty of Engineering, University of Freiburg, Freiburg, Germany.

出版信息

Nat Rev Cardiol. 2022 Sep;19(9):607-619. doi: 10.1038/s41569-022-00677-x. Epub 2022 Apr 8.

Abstract

The 3D nanostructure of the heart, its dynamic deformation during cycles of contraction and relaxation, and the effects of this deformation on cell function remain largely uncharted territory. Over the past decade, the first inroads have been made towards 3D reconstruction of heart cells, with a native resolution of around 1 nm, and of individual molecules relevant to heart function at a near-atomic scale. These advances have provided access to a new generation of data and have driven the development of increasingly smart, artificial intelligence-based, deep-learning image-analysis algorithms. By high-pressure freezing of cardiomyocytes with millisecond accuracy after initiation of an action potential, pseudodynamic snapshots of contraction-induced deformation of intracellular organelles can now be captured. In combination with functional studies, such as fluorescence imaging, exciting insights into cardiac autoregulatory processes at nano-to-micro scales are starting to emerge. In this Review, we discuss the progress in this fascinating new field to highlight the fundamental scientific insight that has emerged, based on technological breakthroughs in biological sample preparation, 3D imaging and data analysis; to illustrate the potential clinical relevance of understanding 3D cardiac nanodynamics; and to predict further progress that we can reasonably expect to see over the next 10 years.

摘要

心脏的 3D 纳米结构、其在收缩和舒张循环期间的动态变形,以及这种变形对细胞功能的影响,在很大程度上仍然是未知领域。在过去的十年中,已经在朝着 3D 重建心脏细胞方面取得了初步进展,其原生分辨率约为 1nm,并且能够以近原子尺度对与心脏功能相关的单个分子进行成像。这些进展为获取新一代数据提供了可能,并推动了越来越智能、基于人工智能的深度学习图像分析算法的发展。通过在动作电位启动后以毫秒级的精度对心肌细胞进行高压冷冻,可以捕捉到收缩诱导的细胞内细胞器变形的拟动态快照。结合荧光成像等功能研究,开始在纳米到微米尺度上对心脏自调节过程有了令人兴奋的深入了解。在这篇综述中,我们讨论了这一迷人的新领域的进展,以突出基于生物样本制备、3D 成像和数据分析方面的技术突破所带来的基本科学见解;说明理解心脏 3D 纳米动力学的潜在临床相关性;并预测未来 10 年我们有望看到的进一步进展。

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