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

机译:多光谱扫描激光眼压检查与光学相干断层扫描相结合,同时进行体内鼠标视网膜成像

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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:已经为体内鼠标视网膜成像开发了一种紧凑的非侵入式多模态系统。它被配置为同时检测来自来自SLO照明光束的扫描激光眼镜(SLO)背散射光的绿色和红色荧光蛋白信号,以及通过光学相干断层扫描(OCT)的关于不同视网膜层的深度信息。同时评估具有不同模式的视网膜特征可以提供有关视网膜神经组织和统治性脉管系统的结构和功能变化的丰富信息。另外,通过自动时间和结构共同登记,同时获取多个通道的分析有助于分析不同方式的数据。作为仪器性能的一个例子,我们将小鼠的视网膜与MICRIGLIA细胞中的GFP组成型表达(CX3CR1〜(GFP / +))进行成像,并且还通过腺泡通过腺体表达穆勒胶质细胞中的红色荧光蛋白麦克白。由GFAP(胶质纤维酸蛋白)启动子驱动的MCHERRY cDNA的相关病毒递送(AAV2)。

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