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Sci Rep ; 7: 42209, 2017 02 06.
Article in English | MEDLINE | ID: mdl-28165052

ABSTRACT

Light-sheet fluorescence microscopy (LSFM) serves to advance developmental research and regenerative medicine. Coupled with the paralleled advances in fluorescence-friendly tissue clearing technique, our cardiac LSFM enables dual-sided illumination to rapidly uncover the architecture of murine hearts over 10 by 10 by 10 mm3 in volume; thereby allowing for localizing progenitor differentiation to the cardiomyocyte lineage and AAV9-mediated expression of exogenous transmembrane potassium channels with high contrast and resolution. Without the steps of stitching image columns, pivoting the light-sheet and sectioning the heart mechanically, we establish a holistic strategy for 3-dimentional reconstruction of the "digital murine heart" to assess aberrant cardiac structures as well as the spatial distribution of the cardiac lineages in neonates and ion-channels in adults.


Subject(s)
Imaging, Three-Dimensional , Myocardium/cytology , Proteins/metabolism , Animals , Animals, Newborn , Calibration , Cell Lineage , Fluorescence , Green Fluorescent Proteins/metabolism , Heart Ventricles/cytology , Mice , Microscopy, Fluorescence , Potassium Channels/metabolism
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