CHERMULA, B., M. BRAZERT, D. IZYCKI, S. CIESIOLKA, W. KRANC, P. CELICHOWSKI, K. OZEGOWSKA, M. J. NAWROCKI, M. JANKOWSKI, Michal JEŠETA, P. ANTOSIK, D. BUKOWSKA, M. T. SKOWRONSKI, K. P. BRUSSOW, M. BRUSKA, L. PAWELCZYK, M. ZABEL, M. NOWICKI a B. KEMPISTY. New Gene Markers of Angiogenesis and Blood Vessels Development in Porcine Ovarian Granulosa Cells during Short-Term Primary Culture In Vitro. Biomed Research International. New York: Hindawi Publishing Corporation, 2019, roč. 2019, č. 2019, s. 1-12. ISSN 2314-6133. Dostupné z: https://dx.doi.org/10.1155/2019/6545210.
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Základní údaje
Originální název New Gene Markers of Angiogenesis and Blood Vessels Development in Porcine Ovarian Granulosa Cells during Short-Term Primary Culture In Vitro
Autoři CHERMULA, B. (616 Polsko), M. BRAZERT (616 Polsko), D. IZYCKI (616 Polsko), S. CIESIOLKA (616 Polsko), W. KRANC (616 Polsko), P. CELICHOWSKI (616 Polsko), K. OZEGOWSKA (616 Polsko), M. J. NAWROCKI (616 Polsko), M. JANKOWSKI (616 Polsko), Michal JEŠETA (203 Česká republika, domácí), P. ANTOSIK (616 Polsko), D. BUKOWSKA (616 Polsko), M. T. SKOWRONSKI (616 Polsko), K. P. BRUSSOW (616 Polsko), M. BRUSKA (616 Polsko), L. PAWELCZYK (616 Polsko), M. ZABEL (616 Polsko), M. NOWICKI (616 Polsko) a B. KEMPISTY (616 Polsko, garant).
Vydání Biomed Research International, New York, Hindawi Publishing Corporation, 2019, 2314-6133.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30214 Obstetrics and gynaecology
Stát vydavatele Velká Británie a Severní Irsko
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 2.276
Kód RIV RIV/00216224:14110/19:00113005
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1155/2019/6545210
UT WoS 000458388600001
Klíčová slova anglicky INDIAN HEDGEHOG; GROWTH; DIFFERENTIATION; DEFICIENCY; ACTIVATION; PREGNANCY; STEMNESS; MATRIX; MICE
Štítky 14110411, rivok
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 5. 5. 2020 09:19.
Anotace
The physiological processes that drive the development of ovarian follicle, as well as the process of oogenesis, are quite well known. Granulosa cells are major players in this occurrence, being the somatic element of the female gamete development. They participate directly in the processes of oogenesis, building the cumulus-oocyte complex surrounding the ovum. In addition to that, they have a further impact on the reproductive processes, being a place of steroid sex hormone synthesis and secretion. It is known that the follicle development creates a major need for angiogenesis and blood vessel development in the ovary. In this study, we use novel molecular approaches to analyze markers of these processes in porcine granulosa cultured primarily in vitro. The cells were recovered from mature sus scrofa specimen after slaughter. They were then subjected to enzymatic digestion and culture primarily for a short term. The RNA was extracted from cultures in specific time periods (0h, 24h, 48h, 96h, and 144h) and analyzed using expression microarrays. The genes that exhibited fold change bigger than |2|, and adjusted p-value lower than 0.05, were considered differentially expressed. From these, we have chosen the members of angiogenesis, blood vessel development, blood vessel morphogenesis, cardiovascular system development, and vasculature development for further selection. CCL2, FGFR2, SFRP2, PDPN, DCN, CAV1, CHI3L1, ITGB3, FN1, and LOX which are upregulated, as well as CXCL10, NEBL, IHH, TGFBR3, SCUBE1, IGF1, EDNRA, RHOB, PPARD, and SLITRK5 genes whose expression is downregulated through the time of culture, were chosen as the potential markers, as their expression varied the most during the time of culture. The fold changes were further validated with RT-qPCR. The genes were described, with special attention to their possible function in GCs during culture. The results broaden the general knowledge about GC's in vitro molecular processes and might serve as a point of reference for further in vivo and clinical studies.
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