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Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin

Comprehensive understanding of the regulatory mechanism of the implantation process in pigs is crucial for reproductive success. The endometrium plays an important role in regulating the establishment and maintenance of gestation. The goal of the current study was to determine the effect of adiponec...

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Autores principales: Smolinska, Nina, Szeszko, Karol, Dobrzyn, Kamil, Kiezun, Marta, Rytelewska, Edyta, Kisielewska, Katarzyna, Gudelska, Marlena, Bors, Kinga, Wyrebek, Joanna, Kopij, Grzegorz, Kaminska, Barbara, Kaminski, Tadeusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470965/
https://www.ncbi.nlm.nih.gov/pubmed/30884816
http://dx.doi.org/10.3390/ijms20061335
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author Smolinska, Nina
Szeszko, Karol
Dobrzyn, Kamil
Kiezun, Marta
Rytelewska, Edyta
Kisielewska, Katarzyna
Gudelska, Marlena
Bors, Kinga
Wyrebek, Joanna
Kopij, Grzegorz
Kaminska, Barbara
Kaminski, Tadeusz
author_facet Smolinska, Nina
Szeszko, Karol
Dobrzyn, Kamil
Kiezun, Marta
Rytelewska, Edyta
Kisielewska, Katarzyna
Gudelska, Marlena
Bors, Kinga
Wyrebek, Joanna
Kopij, Grzegorz
Kaminska, Barbara
Kaminski, Tadeusz
author_sort Smolinska, Nina
collection PubMed
description Comprehensive understanding of the regulatory mechanism of the implantation process in pigs is crucial for reproductive success. The endometrium plays an important role in regulating the establishment and maintenance of gestation. The goal of the current study was to determine the effect of adiponectin on the global expression pattern of genes and relationships among differentially expressed genes (DE-genes) in the porcine endometrium during implantation using microarrays. Diverse transcriptome analyses including gene ontology (GO), biological pathway, networks, and DE-gene analyses were performed. Adiponectin altered the expression of 1286 genes with fold-change (FC) values greater than 1.2 (p < 0.05). The expression of 560 genes were upregulated and 726 downregulated in the endometrium treated with adiponectin. Thirteen genes were selected for real-time PCR validation of differential expression based on a known role in metabolism, steroid and prostaglandin synthesis, interleukin and growth factor action, and embryo implantation. Functional analysis of the relationship between DE-genes indicated that adiponectin interacts with genes that are involved in the processes of cell proliferation, programmed cell death, steroid and prostaglandin synthesis/metabolism, cytokine production, and cell adhesion that are critical for reproductive success. The presented results suggest that adiponectin signalling may play a key role in the implantation of pig.
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spelling pubmed-64709652019-04-26 Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin Smolinska, Nina Szeszko, Karol Dobrzyn, Kamil Kiezun, Marta Rytelewska, Edyta Kisielewska, Katarzyna Gudelska, Marlena Bors, Kinga Wyrebek, Joanna Kopij, Grzegorz Kaminska, Barbara Kaminski, Tadeusz Int J Mol Sci Article Comprehensive understanding of the regulatory mechanism of the implantation process in pigs is crucial for reproductive success. The endometrium plays an important role in regulating the establishment and maintenance of gestation. The goal of the current study was to determine the effect of adiponectin on the global expression pattern of genes and relationships among differentially expressed genes (DE-genes) in the porcine endometrium during implantation using microarrays. Diverse transcriptome analyses including gene ontology (GO), biological pathway, networks, and DE-gene analyses were performed. Adiponectin altered the expression of 1286 genes with fold-change (FC) values greater than 1.2 (p < 0.05). The expression of 560 genes were upregulated and 726 downregulated in the endometrium treated with adiponectin. Thirteen genes were selected for real-time PCR validation of differential expression based on a known role in metabolism, steroid and prostaglandin synthesis, interleukin and growth factor action, and embryo implantation. Functional analysis of the relationship between DE-genes indicated that adiponectin interacts with genes that are involved in the processes of cell proliferation, programmed cell death, steroid and prostaglandin synthesis/metabolism, cytokine production, and cell adhesion that are critical for reproductive success. The presented results suggest that adiponectin signalling may play a key role in the implantation of pig. MDPI 2019-03-16 /pmc/articles/PMC6470965/ /pubmed/30884816 http://dx.doi.org/10.3390/ijms20061335 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Smolinska, Nina
Szeszko, Karol
Dobrzyn, Kamil
Kiezun, Marta
Rytelewska, Edyta
Kisielewska, Katarzyna
Gudelska, Marlena
Bors, Kinga
Wyrebek, Joanna
Kopij, Grzegorz
Kaminska, Barbara
Kaminski, Tadeusz
Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin
title Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin
title_full Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin
title_fullStr Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin
title_full_unstemmed Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin
title_short Transcriptomic Analysis of Porcine Endometrium during Implantation after In Vitro Stimulation by Adiponectin
title_sort transcriptomic analysis of porcine endometrium during implantation after in vitro stimulation by adiponectin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470965/
https://www.ncbi.nlm.nih.gov/pubmed/30884816
http://dx.doi.org/10.3390/ijms20061335
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