Cargando…
Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells
BACKGROUND: Diethylhexyl phthalate (DEHP) is widely used as a plasticizer in polyvinyl chloride products. DEHP exposure, which is widespread in the US, increases preterm birth risk; however, the mechanisms driving this relationship are unclear. Because cyclooxygenase-2 (COX-2) dependent prostaglandi...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462084/ https://www.ncbi.nlm.nih.gov/pubmed/26036283 http://dx.doi.org/10.1186/s12958-015-0046-8 |
_version_ | 1782375611861303296 |
---|---|
author | Tetz, Lauren M Aronoff, David M Loch-Caruso, Rita |
author_facet | Tetz, Lauren M Aronoff, David M Loch-Caruso, Rita |
author_sort | Tetz, Lauren M |
collection | PubMed |
description | BACKGROUND: Diethylhexyl phthalate (DEHP) is widely used as a plasticizer in polyvinyl chloride products. DEHP exposure, which is widespread in the US, increases preterm birth risk; however, the mechanisms driving this relationship are unclear. Because cyclooxygenase-2 (COX-2) dependent prostaglandin synthesis is implicated in preterm birth, we evaluated effects of mono-2-ethylhexyl phthalate (MEHP), the active metabolite of DEHP, on prostaglandin E2 (PGE2) synthesis and COX expression in human placental macrophages (PM). In addition, responses in PM were compared to those in a human macrophage-like cell line, THP-1. METHODS: PM and THP-1 cells were treated for 2, 4, 8, or 24 h with MEHP concentrations ranging from 10 to 180 micromolar. PGE2 concentrations were assessed in culture medium using ELISA, and COX expression was determined by western blot. RESULTS: Treatment of PM and THP-1 cells with 180 micromolar MEHP for 24 h significantly increased PGE2 release. Co-treatment of PMs or THP-1 cells with 180 micromolar MEHP and the non-selective COX inhibitor indomethacin reduced MEHP-stimulated PGE2 production. Similarly, co-treatment of PM and THP-1 cells with the COX-2 selective inhibitor NS-398 resulted in a significant decrease in PGE2, suggesting that MEHP-stimulated PGE2 is dependent specifically on increased COX-2 expression. Western blot analysis revealed a significant increase in COX-2 expression in PM and THP-1 cells treated with 180 micromolar MEHP, and no changes in COX-1 expression, supporting the role of COX-2 in MEHP-stimulated PGE2 synthesis. CONCLUSIONS: The findings from this study are the first to demonstrate phthalate-stimulated PGE2 synthesis in PM and warrant future studies into COX-2-dependent prostaglandin synthesis as a mechanism of toxicant-associated preterm birth. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12958-015-0046-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4462084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44620842015-06-11 Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells Tetz, Lauren M Aronoff, David M Loch-Caruso, Rita Reprod Biol Endocrinol Research BACKGROUND: Diethylhexyl phthalate (DEHP) is widely used as a plasticizer in polyvinyl chloride products. DEHP exposure, which is widespread in the US, increases preterm birth risk; however, the mechanisms driving this relationship are unclear. Because cyclooxygenase-2 (COX-2) dependent prostaglandin synthesis is implicated in preterm birth, we evaluated effects of mono-2-ethylhexyl phthalate (MEHP), the active metabolite of DEHP, on prostaglandin E2 (PGE2) synthesis and COX expression in human placental macrophages (PM). In addition, responses in PM were compared to those in a human macrophage-like cell line, THP-1. METHODS: PM and THP-1 cells were treated for 2, 4, 8, or 24 h with MEHP concentrations ranging from 10 to 180 micromolar. PGE2 concentrations were assessed in culture medium using ELISA, and COX expression was determined by western blot. RESULTS: Treatment of PM and THP-1 cells with 180 micromolar MEHP for 24 h significantly increased PGE2 release. Co-treatment of PMs or THP-1 cells with 180 micromolar MEHP and the non-selective COX inhibitor indomethacin reduced MEHP-stimulated PGE2 production. Similarly, co-treatment of PM and THP-1 cells with the COX-2 selective inhibitor NS-398 resulted in a significant decrease in PGE2, suggesting that MEHP-stimulated PGE2 is dependent specifically on increased COX-2 expression. Western blot analysis revealed a significant increase in COX-2 expression in PM and THP-1 cells treated with 180 micromolar MEHP, and no changes in COX-1 expression, supporting the role of COX-2 in MEHP-stimulated PGE2 synthesis. CONCLUSIONS: The findings from this study are the first to demonstrate phthalate-stimulated PGE2 synthesis in PM and warrant future studies into COX-2-dependent prostaglandin synthesis as a mechanism of toxicant-associated preterm birth. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12958-015-0046-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-03 /pmc/articles/PMC4462084/ /pubmed/26036283 http://dx.doi.org/10.1186/s12958-015-0046-8 Text en © Tetz et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tetz, Lauren M Aronoff, David M Loch-Caruso, Rita Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells |
title | Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells |
title_full | Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells |
title_fullStr | Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells |
title_full_unstemmed | Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells |
title_short | Mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and THP-1 cells |
title_sort | mono-ethylhexyl phthalate stimulates prostaglandin secretion in human placental macrophages and thp-1 cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462084/ https://www.ncbi.nlm.nih.gov/pubmed/26036283 http://dx.doi.org/10.1186/s12958-015-0046-8 |
work_keys_str_mv | AT tetzlaurenm monoethylhexylphthalatestimulatesprostaglandinsecretioninhumanplacentalmacrophagesandthp1cells AT aronoffdavidm monoethylhexylphthalatestimulatesprostaglandinsecretioninhumanplacentalmacrophagesandthp1cells AT lochcarusorita monoethylhexylphthalatestimulatesprostaglandinsecretioninhumanplacentalmacrophagesandthp1cells |