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Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion

The serum amyloid A (SAA) protein is known to function in the acute phase response and immunoregulation. Recently, SAA has been shown to be involved in cell proliferation, differentiation and migratory behavior in different cell types. Here, we evaluated whether exogenous SAA could influence trophob...

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Autores principales: Sandri, Silvana, Urban Borbely, Alexandre, Fernandes, Isabella, Mendes de Oliveira, Edson, Knebel, Franciele Hinterholz, Ruano, Rodrigo, Zugaib, Marcelo, Filippin-Monteiro, Fabiola, Bevilacqua, Estela, Campa, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948705/
https://www.ncbi.nlm.nih.gov/pubmed/24614130
http://dx.doi.org/10.1371/journal.pone.0090881
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author Sandri, Silvana
Urban Borbely, Alexandre
Fernandes, Isabella
Mendes de Oliveira, Edson
Knebel, Franciele Hinterholz
Ruano, Rodrigo
Zugaib, Marcelo
Filippin-Monteiro, Fabiola
Bevilacqua, Estela
Campa, Ana
author_facet Sandri, Silvana
Urban Borbely, Alexandre
Fernandes, Isabella
Mendes de Oliveira, Edson
Knebel, Franciele Hinterholz
Ruano, Rodrigo
Zugaib, Marcelo
Filippin-Monteiro, Fabiola
Bevilacqua, Estela
Campa, Ana
author_sort Sandri, Silvana
collection PubMed
description The serum amyloid A (SAA) protein is known to function in the acute phase response and immunoregulation. Recently, SAA has been shown to be involved in cell proliferation, differentiation and migratory behavior in different cell types. Here, we evaluated whether exogenous SAA could influence trophoblast invasion and differentiation using both the trophoblast-like BeWo cell line and fully differentiated human extravillous trophoblast cells (EVT) isolated from term placentae. SAA stimulated BeWo cell invasion, as measured in Matrigel invasion assays, and induced metalloprotease mRNA expression and activity. Given that BeWo cells express Toll-like receptor 4 (TLR4), a known receptor for SAA, we examined the role of TLR4 in SAA-induced invasion using a TLR4 neutralizing antibody. We also tested whether SAA could affect markers of trophoblast syncytialization in BeWo cells. We observed that SAA decreased βhCG secretion and did not influence trophoblast syncytialization. Using EVT cells isolated from human term basal plates, we confirmed that SAA at 1 and 10 µg/mL doubled EVT invasion in a TLR4-dependent manner, but at 20 µg/mL inhibited EVT cells invasiveness. In addition, we observed that SAA was expressed in both BeWo cells and human term placentae, specifically in the syncytiotrophoblast, decidual cells and EVT. In conclusion, SAA was identified as a molecule that functions in the placental microenvironment to regulate metalloprotease activity and trophoblast invasion, which are key processes in placentation and placental homeostasis.
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spelling pubmed-39487052014-03-13 Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion Sandri, Silvana Urban Borbely, Alexandre Fernandes, Isabella Mendes de Oliveira, Edson Knebel, Franciele Hinterholz Ruano, Rodrigo Zugaib, Marcelo Filippin-Monteiro, Fabiola Bevilacqua, Estela Campa, Ana PLoS One Research Article The serum amyloid A (SAA) protein is known to function in the acute phase response and immunoregulation. Recently, SAA has been shown to be involved in cell proliferation, differentiation and migratory behavior in different cell types. Here, we evaluated whether exogenous SAA could influence trophoblast invasion and differentiation using both the trophoblast-like BeWo cell line and fully differentiated human extravillous trophoblast cells (EVT) isolated from term placentae. SAA stimulated BeWo cell invasion, as measured in Matrigel invasion assays, and induced metalloprotease mRNA expression and activity. Given that BeWo cells express Toll-like receptor 4 (TLR4), a known receptor for SAA, we examined the role of TLR4 in SAA-induced invasion using a TLR4 neutralizing antibody. We also tested whether SAA could affect markers of trophoblast syncytialization in BeWo cells. We observed that SAA decreased βhCG secretion and did not influence trophoblast syncytialization. Using EVT cells isolated from human term basal plates, we confirmed that SAA at 1 and 10 µg/mL doubled EVT invasion in a TLR4-dependent manner, but at 20 µg/mL inhibited EVT cells invasiveness. In addition, we observed that SAA was expressed in both BeWo cells and human term placentae, specifically in the syncytiotrophoblast, decidual cells and EVT. In conclusion, SAA was identified as a molecule that functions in the placental microenvironment to regulate metalloprotease activity and trophoblast invasion, which are key processes in placentation and placental homeostasis. Public Library of Science 2014-03-10 /pmc/articles/PMC3948705/ /pubmed/24614130 http://dx.doi.org/10.1371/journal.pone.0090881 Text en © 2014 Sandri et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sandri, Silvana
Urban Borbely, Alexandre
Fernandes, Isabella
Mendes de Oliveira, Edson
Knebel, Franciele Hinterholz
Ruano, Rodrigo
Zugaib, Marcelo
Filippin-Monteiro, Fabiola
Bevilacqua, Estela
Campa, Ana
Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion
title Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion
title_full Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion
title_fullStr Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion
title_full_unstemmed Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion
title_short Serum Amyloid A in the Placenta and Its Role in Trophoblast Invasion
title_sort serum amyloid a in the placenta and its role in trophoblast invasion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948705/
https://www.ncbi.nlm.nih.gov/pubmed/24614130
http://dx.doi.org/10.1371/journal.pone.0090881
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