2020
Transcriptomic analysis of expression of genes regulating cell cycle progression in porcine ovarian granulosa cells during short-term in vitro primary culture
KULUS, M., W. KRANC, P. SUJKA-KORDOWSKA, P. CELICHOWSKI, A. KONWERSKA et. al.Základní údaje
Originální název
Transcriptomic analysis of expression of genes regulating cell cycle progression in porcine ovarian granulosa cells during short-term in vitro primary culture
Autoři
KULUS, M. (616 Polsko), W. KRANC (616 Polsko), P. SUJKA-KORDOWSKA (616 Polsko), P. CELICHOWSKI (616 Polsko), A. KONWERSKA (616 Polsko), M. JANKOWSKI (616 Polsko), Michal JEŠETA (203 Česká republika, domácí), M. T. SKOWRONSKI (616 Polsko), H. PIOTROWSKA-KEMPISTY (616 Polsko), D. BUKOWSKA (616 Polsko), M. ZABEL (616 Polsko), M. BRUSKA (616 Polsko), P. MOZDZIAK (840 Spojené státy), B. KEMPISTY (616 Polsko, garant) a P. ANTOSIK (616 Polsko)
Vydání
Histochemistry and Cell Biology, New York, Springer, 2020, 0948-6143
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10601 Cell biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.304
Kód RIV
RIV/00216224:14110/20:00116199
Organizační jednotka
Lékařská fakulta
UT WoS
000540794800003
Klíčová slova anglicky
Pig; Ovarian follicle; Granulosa cells; Primary culture; Microarray
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 13. 8. 2020 12:55, Mgr. Tereza Miškechová
Anotace
V originále
The primary function of ovarian granulosa cells (GCs) is the support of oocytes during maturation and development. Molecular analyses of granulosa cell-associated processes, leading to improvement of understanding of the cell cycle events during the formation of ovarian follicles (folliculogenesis), may be key to improve the in vitro fertilization procedures. Primary in vitro culture of porcine GCs was employed to examine the changes in the transcriptomic profile of genes belonging to "cell cycle", "cell division", "cell cycle process", "cell cycle phase transition", "cell cycle G1/S phase transition", "cell cycle G2/M phase transition" and "cell cycle checkpoint" ontology groups. During the analysis, microarrays were employed to study the transcriptome of GCs, analyzing the total RNA of cells from specific periods of in vitro cultures. This research was based on material obtained from 40 landrace gilts of similar weight, age and the same living conditions. RNA was isolated at specific timeframes: before the culture was established (0 h) and after 48 h, 96 h and 144 h in vitro. Out of 133 differentially expressed genes, we chose the 10 most up-regulated (SFRP2,PDPN,PDE3A,FGFR2,PLK2,THBS1,ETS1,LIF,ANXA1,TGFB1) and the 10 most downregulated (IGF1,NCAPD2,CABLES1,H1FOO,NEK2,PPAT,TXNIP,NUP210,RGS2andCCNE2). Some of these genes known to play key roles in the regulation of correct cell cycle passage (up-regulated SFRP2, PDE3A, PLK2, LIF and down-regulated CCNE2, TXNIP, NEK2). The data obtained provide a potential reference for studies on the process of mammalian folliculogenesis, as well as suggests possible new genetic markers for cell cycle progress in in vitro cultured porcine granulosa cells.