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大鼠肾脏活体的传统及共聚焦反射和荧光显微镜检查。

Conventional and confocal epi-reflection and fluorescence microscopy of the rat kidney in vivo.

作者信息

Boyde A, Capasso G, Unwin R J

机构信息

Department of Anatomy and Developmental Biology (Hard Tissue Research Laboratory), University College London, UK.

出版信息

Exp Nephrol. 1998 Sep-Oct;6(5):398-408. doi: 10.1159/000020548.

Abstract

To visualize superficial and accessible renal tubule cells functioning in situ and to relate what we can 'see' to what we know of their function from more invasive in vivo or less direct in vitro studies means applying and adapting recent advances in epifluorescence and confocal microscopy to improve image resolution and to combine this with the use of fluorescent labels to monitor the handling of specific molecules by the proximal and distal renal tubule cells in vivo. Doing this in living tissue is novel, especially in the kidney. Application of confocal microscopy to the imaging of living tissue, as opposed to isolated cells, has not been widely reported. The kidney surface has been imaged before using the confocal microscope and in preliminary studies we have extended this by using a different confocal system with and without fluorescence. While the studies published up to now have been morphological, comparing standard renal (structural) histology of surface glomeruli and renal tubules with the corresponding in vivo confocal images, more dynamic, real-time studies have been limited. Individual red blood cells can be seen flowing around the peritubule capillary network and nucleated white blood cells can also be distinguished. Tubule cells, endothelial cells, the proximal tubule cell brush border and cell mitochondria can be visualized. Filtration and secretion can be observed, and the early and late parts of the proximal tubule distinguished, and the distal tubule recognized. Localization of fluorescently labeled insulin to the luminal brush border and progressive uptake of label and distribution within proximal tubule cells toward the basolateral (blood side) membrane can be demonstrated. The possibility of monitoring hemodynamic changes and tracking the filtration, uptake, secretion and absorption of fluorescently tagged molecules, as well as intracellular fluorescence, e.g. calcium or pH, is an exciting prospect and is ripe for detailed exploration.

摘要

为了观察浅表且易于接近的肾小管细胞在原位的功能,并将我们“看到”的与我们从侵入性更强的体内研究或不太直接的体外研究中所了解的它们的功能联系起来,这意味着要应用和适应落射荧光显微镜和共聚焦显微镜的最新进展,以提高图像分辨率,并将其与使用荧光标记相结合,来监测体内近端和远端肾小管细胞对特定分子的处理情况。在活组织中进行这项操作是新颖的,尤其是在肾脏中。将共聚焦显微镜应用于活组织成像,与分离细胞不同,目前尚未有广泛报道。之前已经使用共聚焦显微镜对肾脏表面进行过成像,在初步研究中,我们通过使用不同的共聚焦系统,在有荧光和无荧光的情况下对其进行了扩展。虽然到目前为止发表的研究都是形态学方面的,将表面肾小球和肾小管的标准肾脏(结构)组织学与相应的体内共聚焦图像进行比较,但更具动态性的实时研究却很有限。可以看到单个红细胞在肾小管周围毛细血管网络中流动,也能区分有核白细胞。肾小管细胞、内皮细胞、近端肾小管细胞刷状缘和细胞线粒体都可以可视化。可以观察到过滤和分泌过程,区分近端肾小管的早期和晚期部分,并识别远端肾小管。可以证明荧光标记的胰岛素在管腔刷状缘的定位,以及标记物在近端肾小管细胞内逐渐摄取并向基底外侧(血侧)膜分布的情况。监测血流动力学变化以及追踪荧光标记分子的过滤、摄取、分泌和吸收,以及细胞内荧光,如钙或pH值,是一个令人兴奋的前景,并且已经成熟,可以进行详细探索。

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