PUBLICATION
            Real-time 3D movement correction for two-photon imaging in behaving animals
- Authors
- Griffiths, V.A., Valera, A.M., Lau, J.Y., Roš, H., Younts, T.J., Marin, B., Baragli, C., Coyle, D., Evans, G.J., Konstantinou, G., Koimtzis, T., Nadella, K.M.N.S., Punde, S.A., Kirkby, P.A., Bianco, I.H., Silver, R.A.
- ID
- ZDB-PUB-200603-15
- Date
- 2020
- Source
- Nature Methods 17(7): 741-748 (Journal)
- Registered Authors
- Bianco, Isaac, Lau, Joanna
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Zebrafish
- Movement
- Male
- Female
- Microscopy, Fluorescence, Multiphoton/methods*
- Imaging, Three-Dimensional/methods*
- Mice
- Animals
- Mice, Inbred C57BL
 
- PubMed
- 32483335 Full text @ Nat. Methods
            Citation
        
        
            Griffiths, V.A., Valera, A.M., Lau, J.Y., Roš, H., Younts, T.J., Marin, B., Baragli, C., Coyle, D., Evans, G.J., Konstantinou, G., Koimtzis, T., Nadella, K.M.N.S., Punde, S.A., Kirkby, P.A., Bianco, I.H., Silver, R.A. (2020) Real-time 3D movement correction for two-photon imaging in behaving animals. Nature Methods. 17(7):741-748.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Two-photon microscopy is widely used to investigate brain function across multiple spatial scales. However, measurements of neural activity are compromised by brain movement in behaving animals. Brain motion-induced artifacts are typically corrected using post hoc processing of two-dimensional images, but this approach is slow and does not correct for axial movements. Moreover, the deleterious effects of brain movement on high-speed imaging of small regions of interest and photostimulation cannot be corrected post hoc. To address this problem, we combined random-access three-dimensional (3D) laser scanning using an acousto-optic lens and rapid closed-loop field programmable gate array processing to track 3D brain movement and correct motion artifacts in real time at up to 1 kHz. Our recordings from synapses, dendrites and large neuronal populations in behaving mice and zebrafish demonstrate real-time movement-corrected 3D two-photon imaging with submicrometer precision.
            
    
        
        
    
    
    
                
                    
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