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 and 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. Online. Histochemistry and Cell Biology. Heidelberg: Springer, 2019, vol. 151, No 2, p. 125-143. ISSN 0948-6143. Available from: https://dx.doi.org/10.1007/s00418-018-1750-1. [citováno 2024-04-23]
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Basic information
Original name 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
Authors KRANC, Wieslawa (616 Poland), Maciej BRAZERT (616 Poland), Joanna BUDNA (616 Poland), Piotr CELICHOWSKI (616 Poland), Artur BRYJA (616 Poland), Mariusz J. NAWROCKI (616 Poland), Katarzyna OZEGOWSKA (616 Poland), Maurycy JANKOWSKI (616 Poland), Blazej CHERMULA (616 Poland), Marta DYSZKIEWICZ-KONWINSKA (616 Poland), Michal JEŠETA (203 Czech Republic, belonging to the institution), Leszek PAWELCZYK (616 Poland), Andrzej BREBOROWICZ (616 Poland), Dominik RACHON (616 Poland), Malgorzata BRUSKA (616 Poland), Michal NOWICKI (616 Poland), Maciej ZABEL (616 Poland) and Bartosz KEMPISTY (616 Poland, guarantor)
Edition Histochemistry and Cell Biology, Heidelberg, Springer, 2019, 0948-6143.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30214 Obstetrics and gynaecology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.418
RIV identification code RIV/00216224:14110/19:00109659
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1007/s00418-018-1750-1
UT WoS 000459058400004
Keywords in English Granulosa cells; Proliferation; Differentiation; Stem cells; Microarrays
Tags 14110411, rivok
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 16/5/2019 11:51.
Abstract
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.
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