Revealing 3D ultrastructure and morphology of stem cell spheroids by electron microscopy
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F17%3APU143838" target="_blank" >RIV/00216305:26620/17:PU143838 - isvavai.cz</a>
Výsledek na webu
<a href="https://www.scopus.com/record/display.uri?eid=2-s2.0-85021355973&origin=resultslist&sort=plf-f&src=s&st1=Revealing+3D+ultrastructure+and+morphology+of+stem+cell+spheroids+by+electron+microscopy&sid=0976ed42b559776de22e21e63e60e432&sot=b&sdt=b&sl=103&s=TI" target="_blank" >https://www.scopus.com/record/display.uri?eid=2-s2.0-85021355973&origin=resultslist&sort=plf-f&src=s&st1=Revealing+3D+ultrastructure+and+morphology+of+stem+cell+spheroids+by+electron+microscopy&sid=0976ed42b559776de22e21e63e60e432&sot=b&sdt=b&sl=103&s=TI</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/978-1-4939-7021-6_30" target="_blank" >10.1007/978-1-4939-7021-6_30</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Revealing 3D ultrastructure and morphology of stem cell spheroids by electron microscopy
Popis výsledku v původním jazyce
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.
Název v anglickém jazyce
Revealing 3D ultrastructure and morphology of stem cell spheroids by electron microscopy
Popis výsledku anglicky
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.
Klasifikace
Druh
J<sub>SC</sub> - Článek v periodiku v databázi SCOPUS
CEP obor
—
OECD FORD obor
10608 - Biochemistry and molecular biology
Návaznosti výsledku
Projekt
<a href="/cs/project/LQ1601" target="_blank" >LQ1601: CEITEC 2020</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Methods in Molecular Biology
ISSN
1940-6029
e-ISSN
—
Svazek periodika
1612
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
15
Strana od-do
417-431
Kód UT WoS článku
—
EID výsledku v databázi Scopus
2-s2.0-85021355973