Litcius/Paper detail

Image restoration of degraded time-lapse microscopy data mediated by near-infrared imaging

Nicola Gritti, Rory M. Power, Alyssa Graves, Jan Huisken

2024Nature Methods15 citationsDOIOpen Access PDF

Abstract

Abstract Time-lapse fluorescence microscopy is key to unraveling biological development and function; however, living systems, by their nature, permit only limited interrogation and contain untapped information that can only be captured by more invasive methods. Deep-tissue live imaging presents a particular challenge owing to the spectral range of live-cell imaging probes/fluorescent proteins, which offer only modest optical penetration into scattering tissues. Herein, we employ convolutional neural networks to augment live-imaging data with deep-tissue images taken on fixed samples. We demonstrate that convolutional neural networks may be used to restore deep-tissue contrast in GFP-based time-lapse imaging using paired final-state datasets acquired using near-infrared dyes, an approach termed InfraRed-mediated Image Restoration (IR 2 ). Notably, the networks are remarkably robust over a wide range of developmental times. We employ IR 2 to enhance the information content of green fluorescent protein time-lapse images of zebrafish and Drosophila embryo/larval development and demonstrate its quantitative potential in increasing the fidelity of cell tracking/lineaging in developing pescoids. Thus, IR 2 is poised to extend live imaging to depths otherwise inaccessible.

Topics & Concepts

Live cell imagingConvolutional neural networkMicroscopyFluorescence-lifetime imaging microscopyFluorescenceArtificial intelligenceComputer scienceBiological systemBiologyOpticsPhysicsCellGeneticsAdvanced Fluorescence Microscopy TechniquesCell Image Analysis TechniquesSpectroscopy Techniques in Biomedical and Chemical Research
Image restoration of degraded time-lapse microscopy data mediated by near-infrared imaging | Litcius