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首页> 外文期刊>Arteriosclerosis, thrombosis, and vascular biology >Imaging and quantitative analysis of atherosclerotic lesions by CARS-based multimodal nonlinear optical microscopy.
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Imaging and quantitative analysis of atherosclerotic lesions by CARS-based multimodal nonlinear optical microscopy.

机译:基于CARS的多峰非线性光学显微镜对动脉粥样硬化病变的成像和定量分析。

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OBJECTIVE: The purpose of this study was to assess the ability of label-free multimodal nonlinear optical (NLO) microscopy to characterize, and thus enable quantitative in situ analyses of, different atherosclerotic lesion types, according to the original scheme suggested by the AHA Committee. METHODS AND RESULTS: Iliac arteries were taken from 24 male Ossabaw pigs divided into lean control and metabolic syndrome groups and were imaged by multimodal NLO microscopy where sum-frequency generation (SFG) and 2-photon excitation fluorescence (TPEF) were integrated on a coherent anti-Stokes Raman scattering (CARS) microscope platform. Foam cells, lipid deposits, matrices, and fibrous caps were visualized with submicron 3D resolution. Starting from the adaptive intimal thickening in the initial stage to the fibrous atheroma or mineralization in the advanced stages, lesions were visualized without labels. Histological staining of each lesion confirmed the lesion stages. Lipid and collagen contents were quantitatively analyzed based on the CARS and SFG signals. Lipid accumulation in thickened intima culminated in type IV whereas the highest collagen deposition was found in Type V lesions. Luminal CARS imaging showed the capability of viewing the location of superficial foam cells that indicate relatively active locus in a lesion artery. CONCLUSIONS: We have demonstrated the capability of CARS-based multimodal NLO microscopy to interrogate different stages of lesion development with subcellular detail to permit quantitative analysis of lipid and collagen contents.
机译:目的:本研究的目的是根据AHA委员会建议的原始方案,评估无标签多峰非线性光学(NLO)显微镜的特征,从而能够对不同的动脉粥样硬化病变类型进行定量原位分析。方法和结果:24动脉取自24只雄性Ossabaw猪,分为瘦对照组和代谢综合征组,并通过多模态NLO显微镜成像,将和频产生(SFG)和2-光子激发荧光(TPEF)整合在一个相干的区域。反斯托克斯拉曼散射(CARS)显微镜平台。泡沫细胞,脂质沉积物,基质和纤维帽以亚微米3D分辨率可视化。从初始阶段的适应性内膜增厚到晚期阶段的纤维性动脉粥样硬化或矿化,可见病变无标记。每个病变的组织学染色证实了病变的阶段。根据CARS和SFG信号定量分析脂质和胶原含量。 IV型高发性内膜中的脂质积累达到最高点,而V型病变中胶原沉积最多。夜光CARS成像显示了查看表面泡沫细胞位置的能力,这些泡沫细胞指示病变动脉中相对活跃的基因座。结论:我们已经证明了基于CARS的多峰NLO显微镜能够通过亚细胞细节询问病变发展的不同阶段,从而能够定量分析脂质和胶原含量。

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