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TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis
In this study levels of prostaglandin E(2) (PGE(2)), tumour necrosis factor (TNF) and interleukin-1 (IL-1) alpha in medium from monocyte derived macrophages (MdM) infected with Chlamydia trachomatis (L(2)/434/Bu or K biovars). TNF and PGE(2) were found in both cases while IL-1 alpha was not detected...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
1993
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365425/ https://www.ncbi.nlm.nih.gov/pubmed/18475547 http://dx.doi.org/10.1155/S0962935193000511 |
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author | Manor, E. Schmitz, E. Sarov, I. |
author_facet | Manor, E. Schmitz, E. Sarov, I. |
author_sort | Manor, E. |
collection | PubMed |
description | In this study levels of prostaglandin E(2) (PGE(2)), tumour necrosis factor (TNF) and interleukin-1 (IL-1) alpha in medium from monocyte derived macrophages (MdM) infected with Chlamydia trachomatis (L(2)/434/Bu or K biovars). TNF and PGE(2) were found in both cases while IL-1 alpha was not detected. Both TNF and PGE(2) levels were higher in the medium of the MdM infected with K biovars. TNF reached maximum levels 24 h postinfection, and then declined, while PGE(2) levels increased continuously during the infection time up to 96 h post-infection. Addition of dexamethasone inhibited production of TNF and PGE(2). Inhibition of PGE(2) production by indomethacin resulted in increased production of TNF, while addition of PGE(2) caused partial inhibition of TNF production from infected MdM. |
format | Text |
id | pubmed-2365425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-23654252008-05-12 TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis Manor, E. Schmitz, E. Sarov, I. Mediators Inflamm Research Article In this study levels of prostaglandin E(2) (PGE(2)), tumour necrosis factor (TNF) and interleukin-1 (IL-1) alpha in medium from monocyte derived macrophages (MdM) infected with Chlamydia trachomatis (L(2)/434/Bu or K biovars). TNF and PGE(2) were found in both cases while IL-1 alpha was not detected. Both TNF and PGE(2) levels were higher in the medium of the MdM infected with K biovars. TNF reached maximum levels 24 h postinfection, and then declined, while PGE(2) levels increased continuously during the infection time up to 96 h post-infection. Addition of dexamethasone inhibited production of TNF and PGE(2). Inhibition of PGE(2) production by indomethacin resulted in increased production of TNF, while addition of PGE(2) caused partial inhibition of TNF production from infected MdM. Hindawi Publishing Corporation 1993 /pmc/articles/PMC2365425/ /pubmed/18475547 http://dx.doi.org/10.1155/S0962935193000511 Text en Copyright © 1993 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ 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 Manor, E. Schmitz, E. Sarov, I. TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis |
title | TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis
|
title_full | TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis
|
title_fullStr | TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis
|
title_full_unstemmed | TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis
|
title_short | TNF and PGE(2) in human monocyte-derived macrophages infected with Chlamydia trachomatis
|
title_sort | tnf and pge(2) in human monocyte-derived macrophages infected with chlamydia trachomatis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365425/ https://www.ncbi.nlm.nih.gov/pubmed/18475547 http://dx.doi.org/10.1155/S0962935193000511 |
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