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

机译:具有双光子显微镜的腔内成像显示甲岩再灌注大鼠心脏中的细胞动力学

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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.
机译:嗜插体显微镜的最新进展已经为健康和病理组织的细胞水平进行了洞察力。然而,跳动心脏的体内蜂窝成像实时尚未完全建立,主要是由于通过心脏和呼吸运动的循环获得清晰的图像。在这里,我们通过心脏手术和新型心脏稳定剂促进的双光子显微镜报道了跳动大鼠心脏的逐个运动图像的成功记录。在15帧/ s的绿色荧光蛋白表达转基因路易斯大鼠中,在心肌细胞中的主要心肌和其亚细胞结构(即核和骨髓纤维纤维素)和线粒体分布的主要心肌组分(即,核和髓纤维)和线粒体分布的亚细胞动力学在绿色荧光蛋白的转基因Lewis大鼠中被视为4-5Ω。我们还观察到缺血/再灌注(I / R)损伤诱导抑制收缩/放松循环,随之而来的心脏组织中的细胞渗透性和白细胞积累的增加。在其他转基因小鼠线中诱导I / R损伤,以进一步阐明心脏组织中的生物事件。该成像系统可以作为动物模型和心脏病药物筛选的实时监测的替代模型,并且可以有助于开发更有效的心脏病治疗。

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