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Intravital microscopy of biosensor activities and intrinsic metabolic states.

Citation
Winfree, S., et al. “Intravital Microscopy Of Biosensor Activities And Intrinsic Metabolic States.”. Methods (San Diego, Calif.), pp. 95-104.
Center Indiana University
Author Seth Winfree, Takashi Hato, Richard N Day
Keywords Biosensor probes, Fluorescence lifetime imaging microscopy (FLIM), Intravital microscopy (IVM), Intrinsic fluorescence, Ratiometric imaging
Abstract

Intravital microscopy (IVM) is an imaging tool that is capable of detecting subcellular signaling or metabolic events as they occur in tissues in the living animal. Imaging in highly scattering biological tissues, however, is challenging because of the attenuation of signal in images acquired at increasing depths. Depth-dependent signal attenuation is the major impediment to IVM, limiting the depth from which significant data can be obtained. Therefore, making quantitative measurements by IVM requires methods that use internal calibration, or alternatively, a completely different way of evaluating the signals. Here, we describe how ratiometric imaging of genetically encoded biosensor probes can be used to make quantitative measurements of changes in the activity of cell signaling pathways. Then, we describe how fluorescence lifetime imaging can be used for label-free measurements of the metabolic states of cells within the living animal.

Year of Publication
2017
Journal
Methods (San Diego, Calif.)
Volume
128
Number of Pages
95-104
Date Published
12/2017
ISSN Number
1095-9130
DOI
10.1016/j.ymeth.2017.04.017
Alternate Journal
Methods
PMID
28434902
PMCID
PMC5776661
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