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Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures
ATP-binding cassette subfamily C (ABCC) genes code for phase III metabolism proteins that translocate xenobiotic (e.g., particulate matter 2.5 (PM(2.5))) and drug metabolites outside the cells. IL-6 secretion is related with the activation of the ABCC transporters. This study assesses ABCC1–4 gene e...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576432/ https://www.ncbi.nlm.nih.gov/pubmed/28900313 http://dx.doi.org/10.1155/2017/6827194 |
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author | Encarnación-Medina, Jarline Rodríguez-Cotto, Rosa I. Bloom-Oquendo, Joseph Ortiz-Martínez, Mario G. Duconge, Jorge Jiménez-Vélez, Braulio |
author_facet | Encarnación-Medina, Jarline Rodríguez-Cotto, Rosa I. Bloom-Oquendo, Joseph Ortiz-Martínez, Mario G. Duconge, Jorge Jiménez-Vélez, Braulio |
author_sort | Encarnación-Medina, Jarline |
collection | PubMed |
description | ATP-binding cassette subfamily C (ABCC) genes code for phase III metabolism proteins that translocate xenobiotic (e.g., particulate matter 2.5 (PM(2.5))) and drug metabolites outside the cells. IL-6 secretion is related with the activation of the ABCC transporters. This study assesses ABCC1–4 gene expression changes and proinflammatory cytokine (IL-6, IL-8) release in human bronchial epithelial cells (BEAS-2B) exposed to PM(2.5) organic extract, budesonide (BUD, used to control inflammation in asthmatic patients), and a cotreatment (Co-T: PM(2.5) and BUD). A real-time PCR assay shows that ABCC1 was upregulated in BEAS-2B exposed after 6 and 7 hr to PM(2.5) extract or BUD but downregulated after 6 hr of the Co-T. ABCC3 was downregulated after 6 hr of BUD and upregulated after 6 hr of the Co-T exposures. ABCC4 was upregulated after 5 hr of PM(2.5) extract, BUD, and the Co-T exposures. The cytokine assay revealed an increase in IL-6 release by BEAS-2B exposed after 5 hr to PM(2.5) extract, BUD, and the Co-T. At 7 hr, the Co-T decreases IL-6 release and IL-8 at 6 hr. In conclusion, the cotreatment showed an opposite effect on exposed BEAS-2B as compared with BUD. The results suggest an interference of the BUD therapeutic potential by PM(2.5). |
format | Online Article Text |
id | pubmed-5576432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-55764322017-09-12 Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures Encarnación-Medina, Jarline Rodríguez-Cotto, Rosa I. Bloom-Oquendo, Joseph Ortiz-Martínez, Mario G. Duconge, Jorge Jiménez-Vélez, Braulio Mediators Inflamm Research Article ATP-binding cassette subfamily C (ABCC) genes code for phase III metabolism proteins that translocate xenobiotic (e.g., particulate matter 2.5 (PM(2.5))) and drug metabolites outside the cells. IL-6 secretion is related with the activation of the ABCC transporters. This study assesses ABCC1–4 gene expression changes and proinflammatory cytokine (IL-6, IL-8) release in human bronchial epithelial cells (BEAS-2B) exposed to PM(2.5) organic extract, budesonide (BUD, used to control inflammation in asthmatic patients), and a cotreatment (Co-T: PM(2.5) and BUD). A real-time PCR assay shows that ABCC1 was upregulated in BEAS-2B exposed after 6 and 7 hr to PM(2.5) extract or BUD but downregulated after 6 hr of the Co-T. ABCC3 was downregulated after 6 hr of BUD and upregulated after 6 hr of the Co-T exposures. ABCC4 was upregulated after 5 hr of PM(2.5) extract, BUD, and the Co-T exposures. The cytokine assay revealed an increase in IL-6 release by BEAS-2B exposed after 5 hr to PM(2.5) extract, BUD, and the Co-T. At 7 hr, the Co-T decreases IL-6 release and IL-8 at 6 hr. In conclusion, the cotreatment showed an opposite effect on exposed BEAS-2B as compared with BUD. The results suggest an interference of the BUD therapeutic potential by PM(2.5). Hindawi 2017 2017-08-16 /pmc/articles/PMC5576432/ /pubmed/28900313 http://dx.doi.org/10.1155/2017/6827194 Text en Copyright © 2017 Jarline Encarnación-Medina 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 Encarnación-Medina, Jarline Rodríguez-Cotto, Rosa I. Bloom-Oquendo, Joseph Ortiz-Martínez, Mario G. Duconge, Jorge Jiménez-Vélez, Braulio Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures |
title | Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures |
title_full | Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures |
title_fullStr | Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures |
title_full_unstemmed | Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures |
title_short | Selective ATP-Binding Cassette Subfamily C Gene Expression and Proinflammatory Mediators Released by BEAS-2B after PM(2.5), Budesonide, and Cotreated Exposures |
title_sort | selective atp-binding cassette subfamily c gene expression and proinflammatory mediators released by beas-2b after pm(2.5), budesonide, and cotreated exposures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576432/ https://www.ncbi.nlm.nih.gov/pubmed/28900313 http://dx.doi.org/10.1155/2017/6827194 |
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