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Slug-expressing mouse prostate epithelial cells have increased stem cell potential

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KAHOUNOVÁ Zuzana REMŠÍK Ján FEDR Radek BOUCHAL Jan MIČKOVÁ Alena SLABÁKOVÁ Eva BINÓ Lucia HAMPL Aleš SOUČEK Karel

Rok publikování 2020
Druh Článek v odborném periodiku
Časopis / Zdroj Stem cell research
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://doi.org/10.1016/j.scr.2020.101844
Doi http://dx.doi.org/10.1016/j.scr.2020.101844
Klíčová slova Prostate stern cells; Epithelial-to-mesenchymal transition; Snai2/Slug; Organoids; Sternness
Popis 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.
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