BRAZERT, M., D. IZYCKI, W. KRANC, B. BOROWIEC, M. POPIS, P. CELICHOWSKI, K. OZEGOWSKA, M. JANKOWSKI, Michal JEŠETA, L. PAWELCZYK, A. BREBOROWICZ, D. RACHON, M. NOWICKI a B. KEMPISTY. TRANSCRIPTOMIC PROFILE OF CELL CYCLE PROGRESSION GENES IN HUMAN OVARIAN GRANULOSA CELLS. Journal of biological regulators and homeostatic agents. Silva Marina: Biolife SAS, 2019, roč. 33, č. 1, s. 39-51. ISSN 0393-974X.
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Základní údaje
Originální název TRANSCRIPTOMIC PROFILE OF CELL CYCLE PROGRESSION GENES IN HUMAN OVARIAN GRANULOSA CELLS
Autoři BRAZERT, M. (616 Polsko), D. IZYCKI (616 Polsko), W. KRANC (616 Polsko), B. BOROWIEC (616 Polsko), M. POPIS (616 Polsko), P. CELICHOWSKI (616 Polsko), K. OZEGOWSKA (616 Polsko), M. JANKOWSKI (616 Polsko), Michal JEŠETA (203 Česká republika, domácí), L. PAWELCZYK (616 Polsko), A. BREBOROWICZ (616 Polsko), D. RACHON (616 Polsko), M. NOWICKI (616 Polsko) a B. KEMPISTY (616 Polsko, garant).
Vydání Journal of biological regulators and homeostatic agents, Silva Marina, Biolife SAS, 2019, 0393-974X.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30214 Obstetrics and gynaecology
Stát vydavatele Itálie
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 1.506
Kód RIV RIV/00216224:14110/19:00113002
Organizační jednotka Lékařská fakulta
UT WoS 000464697500005
Klíčová slova anglicky human ovarian granulosa cells; cell cycle; progression; in vitro
Štítky 14110411, rivok
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 14. 4. 2020 14:38.
Anotace
The ovarian granulosa cells (GCs) that form the structure of follicle undergo substantial modification during the various stages of human folliculogenesis. These modifications include morphological changes, accompanied by differential expression of genes, encoding proteins which are mainly involved in cell growth, proliferation and differentiation. Recent data bring a new insight into the aspects of GCs' stem-like specificity and plasticity, enabling their prolonged proliferation and differentiation into other cell types. This manuscript focuses attention on emerging alterations during GC cell cycle - a series of biochemical and biophysical changes within the cell. Human GCs were collected from follicles of women set to undergo intracytoplasmic sperm injection procedure, as a part of remnant follicular fluid. The cells were primarily cultured for 30 days. Throughout this time, we observed the prominent change in cell morphology from epithelial-like to fibroblast-like, suggesting differentiation to other cell types. Additionally, at days 1, 7, 15 and 30, the RNA was isolated for molecular assays. Using Affymetrie (R) Human Genome U219 Array, we found 2579 human transcripts that were differentially expressed in GCs. From these genes, we extracted 582 Gene Ontology Biological Process (GO BP) Terms and 45 KEGG pathways, among which we investigated transcripts belonging to four GO BPs associated ith cell proliferation: "cell cycle phase transition", "Gl/S phase transition", G2/M phase transition" and "cell cycle checkpoint". Microarray results were validated by RT-qPCR. Increased expression of all the genes studied indicated that increase in GC proliferation during long-term in vitro culture is orchestrated by the up-regulation of genes related to cell cycle control. Furthermore, observed changes in cell morphology may be regulated by a presented set of genes, leading to the induction of pathways specific for sternness plasticity and transdifferentiation in vitro.
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