Quantifiable Intravital Light Sheet Microscopy
- PMID: 35218540
- DOI: 10.1007/978-1-0716-2051-9_11
Quantifiable Intravital Light Sheet Microscopy
Abstract
Live imaging of zebrafish embryos that maintains normal development can be difficult to achieve due to a combination of sample mounting, immobilization, and phototoxicity issues that, once overcome, often still results in image quality sufficiently poor that computer-aided analysis or even manual analysis is not possible. Here, we describe our mounting strategy for imaging the zebrafish midbrain-hindbrain boundary (MHB) with light sheet fluorescence microscopy (LSFM) and pilot experiments to create a study-specific set of parameters for semiautomatically tracking cellular movements in the embryonic midbrain primordium during zebrafish segmentation.
Keywords: Bioimage analysis; Light sheet fluorescence microscopy; Midbrain–hindbrain boundary; Zebrafish.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
References
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- Kesevan G, Machete A, Hans S, Brand M (2020) Cell-fate plasticity, adhesion and cell sorting complementarily establish a sharp midbrain-hindbrain boundary. Development. Development 147:dev185882
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