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Live-Animal Imaging of Renal Function by Multiphoton Microscopy.

Citation
Dunn, K. W., et al. “Live-Animal Imaging Of Renal Function By Multiphoton Microscopy.”. Current Protocols In Cytometry, pp. 12.9.1-12.9.25.
Center Indiana University
Author Kenneth W Dunn, Timothy A Sutton, Ruben M Sandoval
Keywords fluorescence microscopy, in vivo microscopy, intravital microscopy, multiphoton microscopy
Abstract

Intravital microscopy, microscopy of living animals, is a powerful research technique that combines the resolution and sensitivity found in microscopic studies of cultured cells with the relevance and systemic influences of cells in the context of the intact animal. The power of intravital microscopy has recently been extended with the development of multiphoton fluorescence microscopy systems capable of collecting optical sections from deep within the kidney at subcellular resolution, supporting high-resolution characterizations of the structure and function of glomeruli, tubules, and vasculature in the living kidney. Fluorescent probes are administered to an anesthetized, surgically prepared animal, followed by image acquisition for up to 3 hr. Images are transferred via a high-speed network to specialized computer systems for digital image analysis. This general approach can be used with different combinations of fluorescent probes to evaluate processes such as glomerular permeability, proximal tubule endocytosis, microvascular flow, vascular permeability, mitochondrial function, and cellular apoptosis/necrosis. © 2018 by John Wiley & Sons, Inc.

Year of Publication
2018
Journal
Current protocols in cytometry
Volume
83
Number of Pages
12.9.1-12.9.25
Date Published
12/2018
ISSN Number
1934-9300
DOI
10.1002/cpcy.32
Alternate Journal
Curr Protoc Cytom
PMID
29345326
PMCID
PMC5774340
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