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@inbook{2260977,
author = {Sumbal, Jakub and Sumbalová Koledová, Zuzana},
address = {New York},
booktitle = {Mammary Stem Cells},
doi = {http://dx.doi.org/10.1007/978-1-0716-2193-6_14},
editor = {Vivanco, M.d. (eds) Mammary Stem Cells},
keywords = {3D culture; Clearing; Confocal imaging; Microenvironment; Organoid; Staining.},
howpublished = {tištěná verze "print"},
language = {eng},
location = {New York},
isbn = {978-1-0716-2192-9},
pages = {259-269},
publisher = {Springer New York - Humana Press},
title = {Single organoid droplet-based staining method for high-end 3D imaging of mammary organoids},
url = {https://link.springer.com/protocol/10.1007/978-1-0716-2193-6_14},
year = {2022}
}
TY - CHAP
ID - 2260977
AU - Sumbal, Jakub - Sumbalová Koledová, Zuzana
PY - 2022
TI - Single organoid droplet-based staining method for high-end 3D imaging of mammary organoids
VL - Methods in Molecular Biology, vol 2471
PB - Springer New York - Humana Press
CY - New York
SN - 9781071621929
KW - 3D culture
KW - Clearing
KW - Confocal imaging
KW - Microenvironment
KW - Organoid
KW - Staining.
UR - https://link.springer.com/protocol/10.1007/978-1-0716-2193-6_14
N2 - In the last decade, organoids became a tremendously popular technique in developmental and cancer biology for their high pathophysiological relevance to in vivo models with the advantage of easier manipulation, real-time observation, potential for high-throughput studies, and reduced ethical issues. Among other fundamental biological questions, mammary organoids have helped to reveal mechanisms of mammary epithelial morphogenesis, mammary stem cell potential, regulation of lineage specification, mechanisms of breast cancer invasion or resistance to therapy, and their regulation by stromal microenvironment. To exploit the potential of organoid technology to the fullest, together with optimal organoid culture protocols, visualization of organoid architecture and composition in high resolution in three dimensions (3D) is required. Whole-mount imaging of immunolabeled organoids enables preservation of the 3D cellular context, but conventional confocal microscopy of organoid cultures struggles with the large organoid sample size and relatively long distance from the objective to the organoid due to the 3D extracellular matrix (ECM) that surrounds the organoid. We have overcome these issues by physical separation of single organoids with their immediate stroma from the bulk ECM. Here we provide a detail protocol for the procedure, which entails single organoid collection and droplet-based staining and clearing to allow visualization of organoids in the greatest detail.
ER -
SUMBAL, Jakub a Zuzana SUMBALOVÁ KOLEDOVÁ. Single organoid droplet-based staining method for high-end 3D imaging of mammary organoids. In Vivanco, M.d. (eds) Mammary Stem Cells. \textit{Mammary Stem Cells}. New York: Springer New York - Humana Press, 2022, s.~259-269. Methods in Molecular Biology, vol 2471. ISBN~978-1-0716-2192-9. Dostupné z: https://dx.doi.org/10.1007/978-1-0716-2193-6\_{}14.
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