A waveguide imaging platform for live-cell TIRF imaging of neurons over large fields of view.
Ida S OpstadFlorian StröhlMarcus FanthamColin HockingsOliver VanderpoortenFrancesca W van TartwijkJulie Qiaojin LinJean-Claude TinguelyFirehun T DulloGabriele S Kaminski SchierleBalpreet Singh AhluwaliaClemens F KaminskiPublished in: Journal of biophotonics (2020)
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.
Keyphrases
- single molecule
- high resolution
- induced apoptosis
- spinal cord
- high throughput
- cell cycle arrest
- single cell
- stem cells
- risk assessment
- bone marrow
- cell therapy
- blood brain barrier
- spinal cord injury
- photodynamic therapy
- cell free
- brain injury
- extracellular matrix
- quantum dots
- subarachnoid hemorrhage
- label free
- electron microscopy