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1.
Sci Rep ; 8(1): 1647, 2018 01 26.
Article in English | MEDLINE | ID: mdl-29374186

ABSTRACT

In the present study, 3D histochemistry and imaging methodology is described for human gingiva to analyze its vascular network. Fifteen human gingiva samples without signs of inflammation were cleared using a mixture of 2-parts benzyl benzoate and 1-part benzyl alcohol (BABB), after being immunofluorescently stained for CD31, marker of endothelial cells to visualize blood vessels in combination with fluorescent DNA dyes. Samples were imaged in 3D with the use of confocal microscopy and light-sheet microscopy and image processing. BABB clearing caused limited tissue shrinkage 13 ± 7% as surface area and 24 ± 1% as volume. Fluorescence remained intact in BABB-cleared gingiva samples and light-sheet microscopy was an excellent tool to image gingivae whereas confocal microscopy was not. Histochemistry on cryostat sections of gingiva samples after 3D imaging validated structures visualized in 3D. Three-dimensional images showed the vascular network in the stroma of gingiva with one capillary loop in each stromal papilla invading into the epithelium. The capillary loops were tortuous with structural irregularities that were not apparent in 2D images. It is concluded that 3D histochemistry and imaging methodology described here is a promising novel approach to study structural aspects of human gingiva in health and disease.


Subject(s)
Blood Vessels/anatomy & histology , Gingiva/anatomy & histology , Histocytochemistry/methods , Imaging, Three-Dimensional/methods , Optical Imaging/methods , Endothelial Cells/chemistry , Humans , Microscopy , Microscopy, Confocal , Microscopy, Fluorescence , Platelet Endothelial Cell Adhesion Molecule-1/analysis , Staining and Labeling/methods
2.
Prog Histochem Cytochem ; 51(2): 9-23, 2016 08.
Article in English | MEDLINE | ID: mdl-27142295

ABSTRACT

For 3-dimensional (3D) imaging of a tissue, 3 methodological steps are essential and their successful application depends on specific characteristics of the type of tissue. The steps are 1° clearing of the opaque tissue to render it transparent for microscopy, 2° fluorescence labeling of the tissues and 3° 3D imaging. In the past decades, new methodologies were introduced for the clearing steps with their specific advantages and disadvantages. Most clearing techniques have been applied to the central nervous system and other organs that contain relatively low amounts of connective tissue including extracellular matrix. However, tissues that contain large amounts of extracellular matrix such as dermis in skin or gingiva are difficult to clear. The present survey lists methodologies that are available for clearing of tissues for 3D imaging. We report here that the BABB method using a mixture of benzyl alcohol and benzyl benzoate and iDISCO using dibenzylether (DBE) are the most successful methods for clearing connective tissue-rich gingiva and dermis of skin for 3D histochemistry and imaging of fluorescence using light-sheet microscopy.


Subject(s)
Connective Tissue/ultrastructure , Fixatives/chemistry , Histocytochemistry/methods , Imaging, Three-Dimensional/methods , Staining and Labeling/methods , Tissue Fixation/methods , Animals , Benzoates/chemistry , Benzyl Alcohol/chemistry , Fluorescent Dyes/chemistry , Histocytochemistry/instrumentation , Humans , Imaging, Three-Dimensional/instrumentation , Microscopy, Confocal , Phenyl Ethers/chemistry , Specimen Handling/instrumentation , Specimen Handling/methods , Staining and Labeling/instrumentation
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