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双光子显微镜的活体成像揭示了缺血再灌注大鼠心脏中的细胞动力学。

Intravital imaging with two-photon microscopy reveals cellular dynamics in the ischeamia-reperfused rat heart.

机构信息

Department of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.

Research and Development Division for Advanced Technology, Research and Development Center, Dai Nippon Printing Co., Ltd., Tokyo, Japan.

出版信息

Sci Rep. 2018 Oct 30;8(1):15991. doi: 10.1038/s41598-018-34295-w.

Abstract

Recent advances in intravital microscopy have provided insight into dynamic biological events at the cellular level in both healthy and pathological tissue. However, real-time in vivo cellular imaging of the beating heart has not been fully established, mainly due to the difficulty of obtaining clear images through cycles of cardiac and respiratory motion. Here we report the successful recording of clear in vivo moving images of the beating rat heart by two-photon microscopy facilitated by cardiothoracic surgery and a novel cardiac stabiliser. Subcellular dynamics of the major cardiac components including the myocardium and its subcellular structures (i.e., nuclei and myofibrils) and mitochondrial distribution in cardiac myocytes were visualised for 4-5 h in green fluorescent protein-expressing transgenic Lewis rats at 15 frames/s. We also observed ischaemia/reperfusion (I/R) injury-induced suppression of the contraction/relaxation cycle and the consequent increase in cell permeability and leukocyte accumulation in cardiac tissue. I/R injury was induced in other transgenic mouse lines to further clarify the biological events in cardiac tissue. This imaging system can serve as an alternative modality for real time monitoring in animal models and cardiological drug screening, and can contribute to the development of more effective treatments for cardiac diseases.

摘要

近年来,活体显微镜技术的进步为研究健康和病理组织中细胞水平的动态生物学事件提供了新的视角。然而,由于心脏和呼吸运动的循环导致难以获得清晰的图像,实时在体心脏细胞成像尚未完全建立。在这里,我们报告了通过心胸外科手术和新型心脏稳定器,利用双光子显微镜成功记录到清晰的在体跳动大鼠心脏的移动图像。在 GFP 表达的转基因 Lewis 大鼠中,我们以 15 帧/秒的速度观察到主要心脏成分(包括心肌及其亚细胞结构,即细胞核和肌原纤维)和心肌细胞中线粒体分布的亚细胞动力学,持续 4-5 小时。我们还观察到缺血/再灌注(I/R)损伤诱导的收缩/松弛周期抑制以及随后的细胞通透性增加和心脏组织中白细胞聚集。在其他转基因小鼠品系中诱导 I/R 损伤,以进一步阐明心脏组织中的生物学事件。该成像系统可作为动物模型实时监测和心脏药物筛选的替代方式,并有助于开发更有效的心脏疾病治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/411e/6207786/ac5d46af5625/41598_2018_34295_Fig1_HTML.jpg

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