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免疫染色法对小鼠视网膜周细胞的 3D 可视化。

3D Visualization of Retinal Vascular Pericytes in Mice by Immunostaining.

机构信息

Department of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University.

Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences.

出版信息

J Vis Exp. 2024 Nov 1(213). doi: 10.3791/67436.

Abstract

Retinal pericytes are essential for vascular development and stability of the retina, playing a key role in maintaining the integrity of the retinal vasculature. To provide a detailed view of the morphological characteristics of pericytes, this study described a new approach combining the retro-orbital injection of a fluorescent agent, immunofluorescent-staining, and tissue-clearing treatment. Firstly, the fluorescent tomato lectin was injected into the retro-orbital sinus of the live mouse to label the retinal vasculature. After 5 min, the mouse was sacrificed, and its intact retina was carefully removed from the retinal cup and immunofluorescently stained with platelet-derived growth factor receptor β to reveal the pericytes. Additionally, the stained retina was treated with tissue-clearing reagent and whole mounted on the microscope slide. Through these approaches, the retinal vasculature and pericytes were clearly observed in the transparent retina. Under a confocal microscope, we obtained more opportunities to take high-resolution images for further reconstructing and analyzing the morphological characteristics of pericytes along the retinal vascular tree in a three-dimensional view. Methodologically, this protocol offers an effective approach for visualizing pericytes within the retinal vasculature, providing valuable insights into their role under both physiological and pathological conditions.

摘要

视网膜周细胞对于视网膜的血管发育和稳定性至关重要,在维持视网膜血管完整性方面发挥着关键作用。为了更详细地观察周细胞的形态特征,本研究结合了眶后注射荧光剂、免疫荧光染色和组织透明化处理,描述了一种新方法。首先,将荧光番茄凝集素注射到活体小鼠的眶后窦中,以标记视网膜血管。5 分钟后,处死小鼠,小心地从视网膜杯中取出完整的视网膜,并进行血小板衍生生长因子受体 β 的免疫荧光染色,以显示周细胞。此外,对染色的视网膜进行组织透明化处理,并在显微镜载玻片上整体安装。通过这些方法,可以在透明的视网膜中清晰地观察到视网膜血管和周细胞。在共聚焦显微镜下,我们获得了更多机会拍摄高分辨率图像,以便进一步重建和分析沿视网膜血管树的周细胞的形态特征,从三维角度进行观察。从方法学角度来看,该方案为可视化视网膜血管内的周细胞提供了一种有效途径,为其在生理和病理条件下的作用提供了有价值的见解。

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