High resolution microscopy
Slicing embryos gently with laser light sheets
Article first published online: 6 MAR 2012
DOI: 10.1002/bies.201100120
Copyright © 2012 WILEY Periodicals, Inc.
Additional Information
How to Cite
Huisken, J. (2012), Slicing embryos gently with laser light sheets. Bioessays, 34: 406–411. doi: 10.1002/bies.201100120
Publication History
- Issue published online: 16 APR 2012
- Article first published online: 6 MAR 2012
Funded by
- Max Planck Society
- Human Frontiers Science Program (HFSP)
- Abstract
- Article
- References
- Cited By
Keywords:
- cell biology;
- developmental biology;
- light sheet microscopy;
- selective plane illumination microscopy (SPIM);
- zebrafish
Abstract
Light sheet microscopy is an easy to implement and extremely powerful alternative to established fluorescence imaging techniques such as laser scanning confocal, multi-photon and spinning disk microscopy. By illuminating the sample only with a thin slice of light, photo-bleaching is reduced to a minimum, making light sheet microscopy ideal for non-destructive imaging of fragile samples over extended periods of time. Millimeter-sized samples can be imaged rapidly with high resolution and high depth penetration. A large variety of instruments have been developed and optimized for a number of different samples: Bessel beams form thin light sheets for single cells, and selective plane illumination microscopy (SPIM) offers multi-view acquisition to image entire embryos with isotropic resolution. This review explains how light sheet microscopy involves a conceptually new microscope design and how it changes modern imaging in biology.

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