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Multispectral Scanning Laser Ophthalmoscopy combined with Optical Coherence Tomography for simultaneous in vivo mouse retinal imaging

机译:多光谱扫描激光检眼镜结合光学相干断层扫描技术同时进行体内小鼠视网膜成像

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A compact, non-invasive multi-modal system has been developed for in vivo mouse retina imaging. It is configured for simultaneously detecting green and red fluorescent protein signals with scanning laser ophthalmoscopy (SLO) back-scattered light from the SLO illumination beam, and depth information about different retinal layers by means of Optical Coherence Tomography (OCT). Simultaneous assessment of retinal characteristics with different modalities can provide a wealth of information about the structural and functional changes in the retinal neural tissue and chorio-retinal vasculature in vivo. Additionally, simultaneous acquisition of multiple channels facilitates analysis of the data of different modalities by automatic temporal and structural co-registration. As an example of the instrument's performance we imaged the retina of a mouse with constitutive expression of GFP in microglia cells (Cx3cr1~(GFP/+)), and which also expressed the red fluorescent protein mCherry in Mueller glial cells by means of adeno-associated virus delivery (AAV2) of an mCherry cDNA driven by the GFAP (glial fibrillary acid protein) promoter.
机译:已经开发出一种紧凑的,非侵入性的多模式系统,用于体内小鼠视网膜成像。它被配置为通过光学相干断层扫描(OCT)使用来自SLO照明光束的扫描激光检眼镜(SLO)背向散射光以及有关不同视网膜层的深度信息同时检测绿色和红色荧光蛋白信号。同时评估具有不同方式的视网膜特征可以提供有关体内视网膜神经组织和脉络膜-视网膜脉管系统的结构和功能变化的大量信息。另外,同时获取多个通道有助于通过自动时间和结构共配准来分析不同模态的数据。作为该仪器性能的一个例子,我们对在小胶质细胞(Cx3cr1〜(GFP / +))中组成性表达GFP的小鼠的视网膜进行了成像,该小鼠的视网膜中还通过Mueller胶质细胞表达了红色荧光蛋白mCherry。 GFAP(胶质纤维酸性蛋白)启动子驱动的mCherry cDNA的相关病毒传递(AAV2)。

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