| Literature DB >> 33669854 |
Magdalena Kulus1, Wiesława Kranc2, Katarzyna Wojtanowicz-Markiewicz1, Piotr Celichowski3, Agata Światły-Błaszkiewicz4, Eliza Matuszewska4, Patrycja Sujka-Kordowska3,5, Aneta Konwerska3, Maciej Zdun6, Rut Bryl2, Maria Wieczorkiewicz6, Jakub Kulus7, Bogusława Stelmach8, Katarzyna Stefańska3, Joanna Budna-Tukan3, James N Petitte9, Paul Mozdziak9, Kornel Ratajczak1, Jan Matysiak4, Jędrzej M Jaśkowski7, Michał Nowicki3, Bartosz Kempisty1,2,3,9.
Abstract
Changes that occur within oviducts after fertilization are dependent on post-ovulation events, including oocyte-oviduct interactions. Although general processes are well-defined, the molecular basis are poorly understood. Recently, new marker genes involved in 'cell development', 'cell growth', 'cell differentiation' and 'cell maturation' processes have been identified in porcine oocytes. The aim of the study was to assess the expression profile of genes in primary in vitro cultured oviductal epithelial cells (OECs), clustered in Gene Ontology groups which enveloped markers also identified in porcine oocytes. OECs (from 45 gilts) were surgically removed and cultured in vitro for ≤ 30 days, and then subjected to molecular analyses. The transcriptomic and proteomic profiles of cells cultured during 7, 15 and 30 days were investigated. Additionally, morphological/histochemical analyzes were performed. The results of genes expression profiles were validated after using RT-qPCR. The results showed a significant upregulation of UNC45B, NOX4, VLDLR, ITGB3, FMOD, SGCE, COL1A2, LOX, LIPG, THY1 and downregulation of SERPINB2, CD274, TXNIP, CELA1, DDX60, CRABP2, SLC5A1, IDO1, ANPEP, FST. Detailed knowledge of the molecular pathways occurring in the OECs and the gametes that contact them may contribute both to developments of basic science of physiology, and new possibilities in advanced biotechnology of assisted reproduction.Entities:
Keywords: epithelial cells; long-term in vitro culture; microarray assays; oviduct; pig; proteomics; transcriptomics
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Year: 2021 PMID: 33669854 PMCID: PMC7923230 DOI: 10.3390/ijms22042082
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923