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PMID: 12695106 Published · ppublish English Journal Article

High-resolution confocal imaging and three-dimensional rendering.

Methods (San Diego, Calif.) ·Vol. 30 ·No. 1 ·2003-05-00 ·Pages 86-93

Liu YC, Chiang AS

Abstract

Intrinsic opacity and inhomeogeniety of most biological tissues have prevented the efficient light penetration and signal detection for high-resolution confocal imaging of thick tissues. Here, we summarize recent technical advances in high-resolution confocal imaging for visualization of cellular structures and gene expression within intact whole-mount thick tissues. First, we introduce features of the FocusClear technology that render biological tissue transparent and thus improve the light penetration and signal detection. Next, a universal fluorescence staining method that labels all nuclei and membranes is described. We then demonstrate the postrecording image processing techniques for 3D visualization. From these images, regions of interest in the whole-mount brain can be segmented and volume rendered. Together, these technical advances in confocal microscopy allow visualization of structures within whole-mount tissues up to 1mm thick at a resolution similar to that of the observation of single cells in culture. Practical uses and limitations of these techniques are discussed.

MeSH Terms
Animals Brain/anatomy & histology,physiology Cockroaches Female Humans Imaging, Three-Dimensional/methods Microscopy, Confocal/methods
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Liu Yee-Chien
Department of Life Science, National Tsing Hua University, Hsinchu 30043, Taiwan.
Chiang Ann-Shyn
Article Info
Journal
Methods (San Diego, Calif.)
Abbr.
Methods
ISSN
1046-2023
Published
2003-05-00
Pages
86-93
Language
English
Region
United States
NLM ID
9426302
Subset
IM
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