Detailed Information on Publication Record
2017
Revealing 3D Ultrastructure and Morphology of Stem Cell Spheroids by Electron Microscopy
JAROŠ, Josef, Michal PETROV, Markéta TESAŘOVÁ and Aleš HAMPLBasic information
Original name
Revealing 3D Ultrastructure and Morphology of Stem Cell Spheroids by Electron Microscopy
Authors
JAROŠ, Josef (203 Czech Republic, guarantor, belonging to the institution), Michal PETROV (203 Czech Republic), Markéta TESAŘOVÁ (203 Czech Republic) and Aleš HAMPL (203 Czech Republic, belonging to the institution)
Edition
1st. ed. New York, 3D Cell Culture : Methods and Protocols, p. 417-431, 15 pp. Methods in Molecular Biology, volume 1612, 2017
Publisher
Humana Press
Other information
Language
English
Type of outcome
Kapitola resp. kapitoly v odborné knize
Field of Study
10600 1.6 Biological sciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Publication form
printed version "print"
References:
RIV identification code
RIV/00216224:14110/17:00095166
Organization unit
Faculty of Medicine
ISBN
978-1-4939-7019-3
UT WoS
000447757200031
Keywords in English
3D visualization; Image reconstruction; Image segmentation; Morphology; Organoid; SBF-SEM; Scanning electron microscopy; Serial block-face; Spheroid; Stem cell; Ultrastructure
Tags
Tags
International impact, Reviewed
Změněno: 27/4/2020 10:08, Mgr. Tereza Miškechová
Abstract
V originále
Cell culture methods have been developed in efforts to produce biologically relevant systems for developmental and disease modeling, and appropriate analytical tools are essential. Knowledge of ultrastructural characteristics represents the basis to reveal in situ the cellular morphology, cell-cell interactions, organelle distribution, niches in which cells reside, and many more. The traditional method for 3D visualization of ultrastructural components, serial sectioning using transmission electron microscopy (TEM), is very labor-intensive due to contentious TEM slice preparation and subsequent image processing of the whole collection. In this chapter, we present serial block-face scanning electron microscopy, together with complex methodology for spheroid formation, contrasting of cellular compartments, image processing, and 3D visualization. The described technique is effective for detailed morphological analysis of stem cell spheroids, organoids, as well as organotypic cell cultures
Links
EE2.3.20.0185, research and development project |
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GA16-02702S, research and development project |
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MUNI/M/1050/2013, interní kód MU |
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