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Pulse splitter-based nonlinear microscopy for live-cardiomyocyte imaging

机译:基于脉冲分离器的非线性显微镜用于活细胞成像

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摘要

Second harmonic generation (SHG) microscopy is a new imaging technique used in sarcomeric-addition studies. However, during the early stage of cell culture in which sarcomeric additions occur, the neonatal cardiomyocytes that we have been working with are very sensitive to photodamage, the resulting high rate of cell death prevents systematic study of sarcomeric addition using a conventional SHG system. To address this challenge, we introduced use of the pulse-splitter system developed by Na Ji et al. in our two photon excitation fluorescence (TPEF) and SHG hybrid microscope. The system dramatically reduced photodamage to neonatal cardiomyocytes in early stages of culture, greatly increasing cell viability. Thus continuous imaging of live cardiomyocytes was achieved with a stronger laser and for a longer period than has been reported in the literature. The pulse splitter-based TPEF-SHG microscope constructed in this study was demonstrated to be an ideal imaging system for sarcomeric addition-related investigations of neonatal cardiomyocytes in early stages of culture.
机译:二次谐波生成(SHG)显微镜是用于肌节加成研究的一种新的成像技术。但是,在发生添加肌节蛋白的细胞培养的早期阶段,我们一直在研究的新生儿心肌细胞对光损伤非常敏感,由此导致的高细胞死亡率阻止了使用常规SHG系统对肌节蛋白的系统研究。为了应对这一挑战,我们介绍了Na Ji等人开发的脉冲分离器系统的使用。在我们的两个光子激发荧光(TPEF)和SHG混合显微镜中。该系统在培养的早期阶段显着减少了对新生儿心肌细胞的光损伤,从而大大提高了细胞活力。因此,与文献中报道的相比,用更强的激光和更长的时间实现了活心肌细胞的连续成像。这项研究中构建的基于脉冲分离器的TPEF-SHG显微镜被证明是用于培养早期心肌细胞的肌节添加相关研究的理想成像系统。

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