Detailed Information on Publication Record
2020
Slug-expressing mouse prostate epithelial cells have increased stem cell potential
KAHOUNOVÁ, Zuzana, Ján REMŠÍK, Radek FEDR, Jan BOUCHAL, Alena MIČKOVÁ et. al.Basic information
Original name
Slug-expressing mouse prostate epithelial cells have increased stem cell potential
Authors
KAHOUNOVÁ, Zuzana, Ján REMŠÍK (703 Slovakia, belonging to the institution), Radek FEDR, Jan BOUCHAL, Alena MIČKOVÁ, Eva SLABÁKOVÁ, Lucia BINÓ, Aleš HAMPL (203 Czech Republic, belonging to the institution) and Karel SOUČEK (203 Czech Republic, belonging to the institution)
Edition
Stem cell research, Amsterdam, Elsevier, 2020, 1873-5061
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.020
RIV identification code
RIV/00216224:14310/20:00117616
Organization unit
Faculty of Science
UT WoS
000566516300010
Keywords in English
Prostate stern cells; Epithelial-to-mesenchymal transition; Snai2/Slug; Organoids; Sternness
Tags
International impact, Reviewed
Změněno: 16/3/2021 13:05, Mgr. Marie Šípková, DiS.
Abstract
V originále
Deciphering the properties of adult stem cells is crucial for understanding of their role in healthy tissue and in cancer progression as well. Both stem cells and cancer stem cells have shown association with epithelial-to-mesenchymal transition (EMT) in various tissue types. Aiming to investigate the epithelial and mesenchymal phenotypic traits in adult mouse prostate, we sorted subpopulations of basal prostate stem cells (mPSCs) and assessed the expression levels of EMT regulators and markers with custom-designed gene expression array. The population of mPSCs defined by a Lin(-)/Sca-1(+) CD49f(hi)/Trop-2(+) (LSC Trop-(2+)) surface phenotype was enriched in mesenchymal markers, especially EMT master regulator Slug, encoded by the Snail gene. To further dissect the role of Slug in mPSCs, we used transgenic Snai2(tm1.1wbg) reporter mouse strain. Using this model, we confirmed the presence of mesenchymal traits and increase of organoid forming capacity in Slug(+) population of mPSCs. The Slug(+) -derived organoids comprised all prostate epithelial cell types - basal, luminal, and neuroendocrine. Collectively, these data uncover the important role of Slug expression in the physiology of mouse prostate stem cells.
Links
EE2.3.20.0185, research and development project |
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EE2.4.31.0245, research and development project |
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