Histone demethylases JHDM1D, PHF2 and PHF8 expression pattern in granulosa cells obtained from patients undergoing IVF procedure during short-term IVC

Author:

Bryl Rut1,Stefańska Katarzyna2,Chermuła Błażej3,Stelmach Bogumiła3,Pieńkowski Wojciech4,Kulus Jakub5,Perek Joanna1,Wieczorkiewicz Maria6,Wąsiatycz Grzegorz7,Ratajczak Kornel7,Pawelczyk Leszek3,Mozdziak Paul8,Jeseta Michal,Spaczyński Robert Z.3,Bukowska Dorota5

Affiliation:

1. Department of Anatomy , Poznan University of Medical Sciences , Poznań , Poland

2. Department of Histology and Embryology , Poznań University of Medical Sciences , Poznań , Poland

3. Division of Infertility and Reproductive Endocrinology, Department of Gynecology, Obstetrics and Gynecological Oncology , Poznań University of Medical Sciences , Poznań , Poland

4. Division of Perinatology and Women's Diseases , Poznń University of Medical Sciences , Poznań , Poland

5. Department of Diagnostics and Clinical Sciences, Institute of Veterinary Medicine , Nicolaus Copernicus University in Toruń , Toruń , Poland

6. Department of Basic and Preclinical Sciences, Institute of Veterinary Medicine, Faculty of Biological and Veterinary Sciences , Nicolaus Copernicus University in Toruń , Toruń , Poland .

7. Department of Veterinary Surgery, Institute of Veterinary Medicine , Nicolaus Copernicus University in Toruń , Toruń , Poland

8. Physiology Graduate Program , North Carolina State University , Raleigh , NC , USA

Abstract

Abstract Granulosa cells play an important role in follicle development, maturation, and atresia. They are a cellular source of the two most important ovarian steroids, namely, estradiol and progesterone and are also crucial for bidirectional communication with the oocyte, thus being involved in the regulation of its growth, development and function. Growing body of evidence suggests that granulosa cells cultured in vitro display stemness and transdifferentiation potential. Together with the fact that they can be easily collected during IVF procedures, these properties of GCs may be of particular interest for both regenerative medicine and transplantology. Establishment of in vitro cell culture and its thorough characterization, including molecular, is crucial for future potential utilization of human granulosa cells in design of engineered tissue grafts or cell-based therapies, in particular targeted at female infertility. Nevertheless, the transcriptomic alterations which may occur during in vitro culture of granulosa cells are still largely uncharacterized. The aim of this study was to examine expression changes of three genes encoding histone demethylases which serve as transcription coactivators in short term in vitro cell culture of human granulosa cells. The study groups consisted of 14 patients, aged 18–40 years undergoing in vitro fertilization (IVF). Expression level assessment was performed after 24 h, 48 h, 72 h, 96 h, 120 h, 144 h and 168 h of in vitro primary cell culture utilizing RT-qPCR technique. Upregulation of PHF2 expression in all time points of the culture was observed, whereas the tendency of JHDM1D and PHF8 was mainly to decrease in expression level. Further study on a larger population would be required in order to confirm the presented tendencies. Running title: Expression pattern of selected histone demethylases in human granulosa cells

Publisher

Walter de Gruyter GmbH

Subject

Cell Biology,Molecular Biology

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