| Literature DB >> 32067356 |
Ida S Opstad1, Florian Ströhl1,2, Marcus Fantham2, Colin Hockings2, Oliver Vanderpoorten2, Francesca W van Tartwijk2, Julie Qiaojin Lin2,3, Jean-Claude Tinguely1, Firehun T Dullo1, Gabriele S Kaminski-Schierle2, Balpreet S Ahluwalia1, Clemens F Kaminski2.
Abstract
Large fields of view (FOVs) in total internal reflection fluorescence microscopy (TIRFM) via waveguides have been shown to be highly beneficial for single molecule localisation microscopy on fixed cells [1,2] and have also been demonstrated for short-term live-imaging of robust cell types [3-5], but not yet for delicate primary neurons nor over extended periods of time. Here, we present a waveguide-based TIRFM set-up for live-cell imaging of demanding samples. Using the developed microscope, referred to as the ChipScope, we demonstrate successful culturing and imaging of fibroblasts, primary rat hippocampal neurons and axons of Xenopus retinal ganglion cells (RGCs). The high contrast and gentle illumination mode provided by TIRFM coupled with the exceptionally large excitation areas and superior illumination homogeneity offered by photonic waveguides have potential for a wide application span in neuroscience applications.Mesh:
Year: 2020 PMID: 32067356 DOI: 10.1002/jbio.201960222
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207