Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Biomedical Imaging Unit, University of Southampton, Southampton, UK.
Methods Mol Biol. 2020;2150:167-182. doi: 10.1007/7651_2019_223.
The transport and targeting of internalized molecules to distinct intracellular organelles/compartments can prove challenging to visualize clearly, which can contribute to some of the difficulties associated with these studies. By combining several approaches, we show how the trafficking and processing of photoreceptor outer segments in the phagosome and autophagy-lysosomal pathways of the retinal pigment epithelium (RPE) can easily be quantified and visualized as 3D-reconstructed images. This protocol takes advantage of new developments in microscopy and image-analysis software which has the potential to help better understand dynamic intracellular processes that underlie RPE dysfunction associated with irreversible blinding diseases such as age-related macular degeneration. The method described herein can also be used to study the trafficking and co-localization of different intracellular cargos in other cell types and tissues.
将内化分子运输和靶向到不同的细胞内细胞器/隔室可能难以清晰地可视化,这可能是这些研究中存在一些困难的原因之一。通过结合几种方法,我们展示了如何在吞噬体和视网膜色素上皮(RPE)的自噬溶酶体途径中对光感受器外节的运输和处理进行定量和可视化,作为 3D 重建图像。该方案利用了显微镜和图像分析软件的新发展,这有可能有助于更好地理解与年龄相关性黄斑变性等不可逆转致盲疾病相关的 RPE 功能障碍的基础上的动态细胞内过程。本文所述的方法也可用于研究其他细胞类型和组织中不同细胞内货物的运输和共定位。