KRANC, Wieslawa, Maciej BRAZERT, Joanna BUDNA, Piotr CELICHOWSKI, Artur BRYJA, Mariusz J. NAWROCKI, Katarzyna OZEGOWSKA, Maurycy JANKOWSKI, Blazej CHERMULA, Marta DYSZKIEWICZ-KONWINSKA, Michal JEŠETA, Leszek PAWELCZYK, Andrzej BREBOROWICZ, Dominik RACHON, Malgorzata BRUSKA, Michal NOWICKI, Maciej ZABEL a Bartosz KEMPISTY. Genes responsible for proliferation, differentiation, and junction adhesion are significantly up-regulated in human ovarian granulosa cells during a long-term primary in vitro culture. Histochemistry and Cell Biology. Heidelberg: Springer, 2019, roč. 151, č. 2, s. 125-143. ISSN 0948-6143. Dostupné z: https://dx.doi.org/10.1007/s00418-018-1750-1.
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Základní údaje
Originální název Genes responsible for proliferation, differentiation, and junction adhesion are significantly up-regulated in human ovarian granulosa cells during a long-term primary in vitro culture
Autoři KRANC, Wieslawa (616 Polsko), Maciej BRAZERT (616 Polsko), Joanna BUDNA (616 Polsko), Piotr CELICHOWSKI (616 Polsko), Artur BRYJA (616 Polsko), Mariusz J. NAWROCKI (616 Polsko), Katarzyna OZEGOWSKA (616 Polsko), Maurycy JANKOWSKI (616 Polsko), Blazej CHERMULA (616 Polsko), Marta DYSZKIEWICZ-KONWINSKA (616 Polsko), Michal JEŠETA (203 Česká republika, domácí), Leszek PAWELCZYK (616 Polsko), Andrzej BREBOROWICZ (616 Polsko), Dominik RACHON (616 Polsko), Malgorzata BRUSKA (616 Polsko), Michal NOWICKI (616 Polsko), Maciej ZABEL (616 Polsko) a Bartosz KEMPISTY (616 Polsko, garant).
Vydání Histochemistry and Cell Biology, Heidelberg, Springer, 2019, 0948-6143.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30214 Obstetrics and gynaecology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 3.418
Kód RIV RIV/00216224:14110/19:00109659
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1007/s00418-018-1750-1
UT WoS 000459058400004
Klíčová slova anglicky Granulosa cells; Proliferation; Differentiation; Stem cells; Microarrays
Štítky 14110411, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 16. 5. 2019 11:51.
Anotace
The human ovarian granulosa cells (GCs) surround the oocyte and form the proper architecture of the ovarian follicle. The ability of GCs to proliferate and differentiate in the conditions of in vitro culture has been proven. However, there is still a large field for extensive investigation of molecular basics, as well as marker genes, responsible for these processes. This study aimed to find the new marker genes, encoding proteins that regulate human GCs in vitro capability for proliferation and differentiation during long-term primary culture. The human follicular GCs were collected from hyper-stimulated ovarian follicles during IVF procedures and transferred to a long-term in vitro culture. The culture lasted for 30 days, with RNA samples isolated at days 1, 7, 15, 30. Transcriptomic analysis was then performed with the use of Affymetrix microarray. Obtained results were then subjected to bioinformatical evaluation and sorting. After subjecting the datasets to KEGG analysis, three differentially expressed ontology groups cell differentiation (GO:0030154), cell proliferation (GO:0008283) and cell-cell junction organization (GO:0045216) were chosen for further investigation. All three of those ontology groups are involved in human GCs' in vitro lifespan, proliferation potential, and survival capability. Changes in expression of genes of interest belonging to the chosen GOs were validated with the use of RT-qPCR. In this manuscript, we suggest that VCL, PARVA, FZD2, NCS1, and COL5A1 may be recognized as new markers of GC in vitro differentiation, while KAT2B may be a new marker of their proliferation. Additionally, SKI, GLI2, FERMT2, and CDH2 could also be involved in GC in vitro proliferation and differentiation processes. We demonstrated that, in long-term in vitro culture, GCs exhibit markers that suggest their ability to differentiate into different cells types. Therefore, the higher expression profile of these genes may also be associated with the induction of cellular differentiation processes that take place beyond the long-term primary in vitro culture.
VytisknoutZobrazeno: 23. 7. 2024 21:23