Detailed Information on Publication Record
2017
Lungosphere Assay: 3D Culture of Lung Epithelial Stem/Progenitor Cells
RABATA, Anas, Aleš HAMPL and Zuzana KOLEDOVÁBasic information
Original name
Lungosphere Assay: 3D Culture of Lung Epithelial Stem/Progenitor Cells
Authors
RABATA, Anas (760 Syrian Arab Republic, belonging to the institution), Aleš HAMPL (203 Czech Republic, belonging to the institution) and Zuzana KOLEDOVÁ (703 Slovakia, guarantor, belonging to the institution)
Edition
1st. ed. New York, 3D Cell Culture : Methods and Protocols, p. 149-165, 17 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/00216224:14110/17:00095147
Organization unit
Faculty of Medicine
ISBN
978-1-4939-7019-3
UT WoS
000447757200012
Keywords in English
3D culture; Lung epithelial stem/progenitor cells; Lungosphere assay; Spheroid culture
Tags
Tags
International impact, Reviewed
Změněno: 27/4/2020 09:05, Mgr. Tereza Miškechová
Abstract
V originále
Lung epithelium contains distinctive subpopulations of lung stem/progenitor cells (LSPCs) that are essential for lung epithelial maintenance and repair in vivo. Hence, LSPCs are in the center of interest of lung biology due to their promising therapeutic applications. To reach this goal, proper characterization of LSPCs, understanding of their proliferation and differentiation potentials and elucidation of mechanisms that control them are necessary. Therefore, development of reliable in vitro clonogenic assays has been needed. We established lungosphere assay, an in vitro sphere-forming 3D culture assay that enables to evaluate stem/progenitor cell activity, self-renewal and differentiation capacity of LSPCs and to conveniently test the effect of various treatments on LSPCs. Here we provide a detailed description of procedures for isolation of adult mouse lung epithelial cells, their culture in non-adherent conditions to form LSPC-derived spheroids (lungospheres) and for embedding of lungospheres into 3D extracellular matrix to model processes of lung tissue maintenance in a physiologically relevant microenvironment.
Links
GJ16-20031Y, research and development project |
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NV16-31501A, research and development project |
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ROZV/20/LF/2015, interní kód MU |
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