Imaging of cellular dynamics in vitro and in situ: from a whole organism to sub-cellular imaging with self-driving, multi-scale microscopy
Daetwyler, S.; Mazloom-Farsibaf, H.; Zhou, F. Y.; Segal, D.; Sapoznik, E.; Westcott, J. M.; Brekken, R. A.; Danuser, G.; Fiolka, R. P.
Show abstract
Many biological processes span multiple time and length scales, including developmental processes and cancer metastasis. While light-sheet fluorescence microscopy (LSFM) has become a fast and efficient method for imaging of organisms, cells and sub-cellular dynamics, simultaneous observations across these scales have remained challenging. Moreover, continuous high-resolution imaging inside living organisms has mostly been limited to few hours as regions of interest quickly move out of view due to sample movement and growth. Here, we present a self-driving, multi-resolution light-sheet microscope platform controlled by a custom Python-based software, to simultaneous observe and quantify sub-cellular dynamics and entire organisms in vitro and in vivo over hours of imaging. We apply the platform to the study of developmental processes, cancer invasion and metastasis, and we provide quantitative multi-scale analysis of immune-cancer cell interactions in zebrafish xenografts.
Matching journals
The top 1 journal accounts for 50% of the predicted probability mass.
Similar papers in this journal
- Kilohertz volumetric imaging of in-vivo dynamics using squeezed light field microscopy 99%
- Resolution doubling in light-sheet microscopy via oblique plane structured illumination 98%
- View-channel-depth light-field microscopy: real-time volumetric reconstruction of biological dynamics by deep learning 98%
Similar papers in this journal
- Zero-shot learning enables instant denoising and super-resolution in optical fluorescence microscopy 99%
- Minutes-timescale 3D isotropic imaging of entire organs at subcellular resolution by content-aware compressed-sensing light-sheet microscopy 98%
- Smart hybrid microscopy for cell-friendlydetection of rare events 98%
Similar papers in this journal
- Quantitatively mapping local quality of super-resolution microscopy by rolling Fourier ring correlation 97%
- Excitation spectral microscopy for highly multiplexed fluorescence imaging and quantitative biosensing 97%
- Extended-depth of field random illumination microscopy, EDF-RIM, provides super-resolved projective imaging 94%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.