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Scanning light-sheet microscopy in the whole mouse brain with HiLo background rejection

Open access
Mertz, Jerome, Kim, Jinhyun·2010·Journal of Biomedical Optics

Abstract

It is well known that light-sheet illumination can enable optically sectioned wide-field imaging of macroscopic samples. However, the optical sectioning capacity of a light-sheet macroscope is undermined by sample-induced scattering or aberrations that broaden the thickness of the sheet illumination. We present a technique to enhance the optical sectioning capacity of a scanning light-sheet microscope by out-of-focus background rejection. The technique, called HiLo microscopy, makes use of two images sequentially acquired with uniform and structured sheet illumination. An optically sectioned image is then synthesized by fusing high and low spatial frequency information from both images. The benefits of combining light-sheet macroscopy and HiLo background rejection are demonstrated in optically cleared whole mouse brain samples, using both green fluorescent protein (GFP)-fluorescence and dark-field scattered light contrast.

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Metadata

Authors
Mertz, J., & Kim, J.
Venue
Journal of Biomedical Optics
Published
2010-01-01
Volume
15
Issue
01
Pages
1
ISSN
1083-3668 (ISSN-L)
OpenAlex
W2098681947
Cited by
183
References
0
FWCI
6.74
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Scanning light-sheet microscopy in the whole mouse brain with HiLo background rejection. https://app.cochat.ai/papers/10.1117/1.3324890
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Mertz, J., & Kim, J. (2010). Scanning light-sheet microscopy in the whole mouse brain with HiLo background rejection. Journal of Biomedical Optics. https://doi.org/10.1117/1.3324890

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.