Litcius/Paper detail

3D super-resolution deep-tissue imaging in living mice

Mary Grace M. Velasco, Mengyang Zhang, Jacopo Antonello, Peng Yuan, Edward S. Allgeyer, Dennis May, Ons M’Saad, Phylicia Kidd, Andrew E. S. Barentine, Valentina Greco, Jaime Grutzendler, Martin J. Booth, Joerg Bewersdorf

2021Optica77 citationsDOIOpen Access PDF

Abstract

Stimulated emission depletion (STED) microscopy enables the three-dimensional (3D) visualization of dynamic nanoscale structures in living cells, offering unique insights into their organization. However, 3D-STED imaging deep inside biological tissue is obstructed by optical aberrations and light scattering. We present a STED system that overcomes these challenges. Through the combination of two-photon excitation, adaptive optics, red-emitting organic dyes, and a long-working-distance water-immersion objective lens, our system achieves aberration-corrected 3D super-resolution imaging, which we demonstrate 164 µm deep in fixed mouse brain tissue and 76 µm deep in the brain of a living mouse.

Topics & Concepts

MicroscopySTED microscopyBrain tissueLight sheet fluorescence microscopyVisualizationOptical imagingBiomedical engineeringBiologyComputer visionFluorescence microscopeNervous systemBright-field microscopyNeuroscienceFluorescence-lifetime imaging microscopyAnatomyArtificial intelligenceMedicineBiological tissueOpticsAdvanced Fluorescence Microscopy TechniquesLuminescence and Fluorescent MaterialsNonlinear Optical Materials Studies
3D super-resolution deep-tissue imaging in living mice | Litcius