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Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile

Mesenchymal stem cells (MSCs) were isolated and characterized from postpartum bovine endometrium of animals with subclinical (n = 5) and clinical endometritis (n = 3) and healthy puerperal females (n = 5). Cells isolated displayed mean morphological features of MSCs and underwent osteogenic, chondro...

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Autores principales: Lara, Evelyn, Velásquez, Alejandra, Cabezas, Joel, Rivera, Nathaly, Pacha, Paulina, Rodríguez-Alvarez, Lleretny, Saravia, Fernando, Castro, Fidel Ovidio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682089/
https://www.ncbi.nlm.nih.gov/pubmed/29213289
http://dx.doi.org/10.1155/2017/4297639
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author Lara, Evelyn
Velásquez, Alejandra
Cabezas, Joel
Rivera, Nathaly
Pacha, Paulina
Rodríguez-Alvarez, Lleretny
Saravia, Fernando
Castro, Fidel Ovidio
author_facet Lara, Evelyn
Velásquez, Alejandra
Cabezas, Joel
Rivera, Nathaly
Pacha, Paulina
Rodríguez-Alvarez, Lleretny
Saravia, Fernando
Castro, Fidel Ovidio
author_sort Lara, Evelyn
collection PubMed
description Mesenchymal stem cells (MSCs) were isolated and characterized from postpartum bovine endometrium of animals with subclinical (n = 5) and clinical endometritis (n = 3) and healthy puerperal females (n = 5). Cells isolated displayed mean morphological features of MSCs and underwent osteogenic, chondrogenic, and adipogenic differentiation after induction (healthy and subclinical). Cells from cows with clinical endometritis did not undergo adipogenic differentiation. All cells expressed mRNAs for selected MSC markers. Endometrial MSCs were challenged in vitro with PGE(2) at concentrations of 0, 1, 3, and 10 μM, and their global transcriptomic profile was studied. Overall, 1127 genes were differentially expressed between unchallenged cells and cells treated with PGE(2) at all concentrations (763 up- and 364 downregulated, fold change > 2, and P < 0.05). The pathways affected the most by the PGE(2) challenge were immune response, angiogenesis, and cell proliferation. In conclusion, we demonstrated that healthy puerperal bovine endometrium contains MSCs and that endometritis modifies and limits some functional characteristics of these cells, such as their ability to proceed to adipogenic differentiation. Also, PGE(2), an inflammatory mediator of endometritis, modifies the transcriptomic profile of endometrial MSCs. A similar situation may occur during inflammation associated with endometritis, therefore affecting the main properties of endometrial MSCs.
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spelling pubmed-56820892017-12-06 Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile Lara, Evelyn Velásquez, Alejandra Cabezas, Joel Rivera, Nathaly Pacha, Paulina Rodríguez-Alvarez, Lleretny Saravia, Fernando Castro, Fidel Ovidio Stem Cells Int Research Article Mesenchymal stem cells (MSCs) were isolated and characterized from postpartum bovine endometrium of animals with subclinical (n = 5) and clinical endometritis (n = 3) and healthy puerperal females (n = 5). Cells isolated displayed mean morphological features of MSCs and underwent osteogenic, chondrogenic, and adipogenic differentiation after induction (healthy and subclinical). Cells from cows with clinical endometritis did not undergo adipogenic differentiation. All cells expressed mRNAs for selected MSC markers. Endometrial MSCs were challenged in vitro with PGE(2) at concentrations of 0, 1, 3, and 10 μM, and their global transcriptomic profile was studied. Overall, 1127 genes were differentially expressed between unchallenged cells and cells treated with PGE(2) at all concentrations (763 up- and 364 downregulated, fold change > 2, and P < 0.05). The pathways affected the most by the PGE(2) challenge were immune response, angiogenesis, and cell proliferation. In conclusion, we demonstrated that healthy puerperal bovine endometrium contains MSCs and that endometritis modifies and limits some functional characteristics of these cells, such as their ability to proceed to adipogenic differentiation. Also, PGE(2), an inflammatory mediator of endometritis, modifies the transcriptomic profile of endometrial MSCs. A similar situation may occur during inflammation associated with endometritis, therefore affecting the main properties of endometrial MSCs. Hindawi 2017 2017-10-29 /pmc/articles/PMC5682089/ /pubmed/29213289 http://dx.doi.org/10.1155/2017/4297639 Text en Copyright © 2017 Evelyn Lara et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lara, Evelyn
Velásquez, Alejandra
Cabezas, Joel
Rivera, Nathaly
Pacha, Paulina
Rodríguez-Alvarez, Lleretny
Saravia, Fernando
Castro, Fidel Ovidio
Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile
title Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile
title_full Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile
title_fullStr Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile
title_full_unstemmed Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile
title_short Endometritis and In Vitro PGE(2) Challenge Modify Properties of Cattle Endometrial Mesenchymal Stem Cells and Their Transcriptomic Profile
title_sort endometritis and in vitro pge(2) challenge modify properties of cattle endometrial mesenchymal stem cells and their transcriptomic profile
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682089/
https://www.ncbi.nlm.nih.gov/pubmed/29213289
http://dx.doi.org/10.1155/2017/4297639
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