» Articles » PMID: 33996235

Single-scan HiLo with Line-illumination Strategy for Optical Section Imaging of Thick Tissues

Overview
Specialty Radiology
Date 2021 May 17
PMID 33996235
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Optical sectioning has been widely employed for inhibiting out-of-focus backgrounds in three-dimensional (3D) imaging of biological samples. However, point scanning imaging or multiple acquisitions for wide-field optical sectioning in epi-illumination microscopy remains time-consuming for large-scale imaging. In this paper, we propose a single-scan optical sectioning method based on the hybrid illumination (HiLo) algorithm with a line-illumination strategy. Our method combines HiLo background inhibition with confocal slit detection. It thereby offers a higher optical sectioning capability than wide-field HiLo and line-confocal imaging without extra modulation and multiple data acquisition. To demonstrate the optical-sectioning capability of our system, we imaged a thin fluorescent plane and different fluorescence-labeled mouse tissue. Our method shows an excellent background inhibition in thick tissue and thus potentially provides an alternative tool for 3D imaging of large-scale biological tissue.

Citing Articles

Optical sectioning methods in three-dimensional bioimaging.

Zhang J, Qiao W, Jin R, Li H, Gong H, Chen S Light Sci Appl. 2024; 14(1):11.

PMID: 39741128 PMC: 11688461. DOI: 10.1038/s41377-024-01677-x.


3D autofluorescence imaging of hydronephrosis and renal anatomical structure using cryo-micro-optical sectioning tomography.

Fan G, Jiang C, Huang Z, Tian M, Pan H, Cao Y Theranostics. 2023; 13(14):4885-4904.

PMID: 37771780 PMC: 10526660. DOI: 10.7150/thno.86695.


Superresolution structured illumination microscopy reconstruction algorithms: a review.

Chen X, Zhong S, Hou Y, Cao R, Wang W, Li D Light Sci Appl. 2023; 12(1):172.

PMID: 37433801 PMC: 10336069. DOI: 10.1038/s41377-023-01204-4.


Cryo-fluorescence micro-optical sectioning tomography for volumetric imaging of various whole organs with subcellular resolution.

Deng L, Chen J, Li Y, Han Y, Fan G, Yang J iScience. 2022; 25(8):104805.

PMID: 35992061 PMC: 9389242. DOI: 10.1016/j.isci.2022.104805.


High-speed mosaic imaging using scanner-synchronized stage position sampling.

Huang C, Ching-Roa V, Liu Y, Giacomelli M J Biomed Opt. 2022; 27(1).

PMID: 35075830 PMC: 8786391. DOI: 10.1117/1.JBO.27.1.016502.


References
1.
Lim D, Chu K, Mertz J . Wide-field fluorescence sectioning with hybrid speckle and uniform-illumination microscopy. Opt Lett. 2008; 33(16):1819-21. DOI: 10.1364/ol.33.001819. View

2.
Lein E, Hawrylycz M, Ao N, Ayres M, Bensinger A, Bernard A . Genome-wide atlas of gene expression in the adult mouse brain. Nature. 2006; 445(7124):168-76. DOI: 10.1038/nature05453. View

3.
Mertz J, Kim J . Scanning light-sheet microscopy in the whole mouse brain with HiLo background rejection. J Biomed Opt. 2010; 15(1):016027. PMC: 2917465. DOI: 10.1117/1.3324890. View

4.
Lin W, Wang D, Meng Y, Chen S . Multi-focus microscope with HiLo algorithm for fast 3-D fluorescent imaging. PLoS One. 2019; 14(9):e0222729. PMC: 6754165. DOI: 10.1371/journal.pone.0222729. View

5.
Neil M, Juskaitis R, Wilson T . Method of obtaining optical sectioning by using structured light in a conventional microscope. Opt Lett. 2008; 22(24):1905-7. DOI: 10.1364/ol.22.001905. View