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Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6

Increased plasma- and tissue levels of endothelin-1 (ET-1) during inflammatory diseases, have suggested a role of ET-1 in the pathophysiology of inflammatory reactions. The authors have studied the effect of ET-1 on cytokine release from monocytes and monocyte-derived macrophages. ET-1 increased sec...

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Detalles Bibliográficos
Autores principales: Helset, E., Sildnes, T., Seljelid, R., Konopski, Z.S.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365438/
https://www.ncbi.nlm.nih.gov/pubmed/18475557
http://dx.doi.org/10.1155/S0962935193000596
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author Helset, E.
Sildnes, T.
Seljelid, R.
Konopski, Z.S.
author_facet Helset, E.
Sildnes, T.
Seljelid, R.
Konopski, Z.S.
author_sort Helset, E.
collection PubMed
description Increased plasma- and tissue levels of endothelin-1 (ET-1) during inflammatory diseases, have suggested a role of ET-1 in the pathophysiology of inflammatory reactions. The authors have studied the effect of ET-1 on cytokine release from monocytes and monocyte-derived macrophages. ET-1 increased secretion of TNF-α, IL-1β and IL-6 in a dose- and time-dependent manner. Optimal ET-1 concentration ranged from 0.01 to 1 nM. The maximal response was a 200 to 400% increase in cytokine release. A time-course study revealed that the pattern of cytokines induced by ET-1 was different in monocytes and macrophages, although an early increase in TNF-α was observed in both monocyte and macrophage supernatants. In conclusion, ET-1 stimulates monocytes and macrophages to release cytokines thereby demonstrating a potential role for ET-1 in regulation of inflammatory responses.
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spelling pubmed-23654382008-05-12 Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6 Helset, E. Sildnes, T. Seljelid, R. Konopski, Z.S. Mediators Inflamm Research Article Increased plasma- and tissue levels of endothelin-1 (ET-1) during inflammatory diseases, have suggested a role of ET-1 in the pathophysiology of inflammatory reactions. The authors have studied the effect of ET-1 on cytokine release from monocytes and monocyte-derived macrophages. ET-1 increased secretion of TNF-α, IL-1β and IL-6 in a dose- and time-dependent manner. Optimal ET-1 concentration ranged from 0.01 to 1 nM. The maximal response was a 200 to 400% increase in cytokine release. A time-course study revealed that the pattern of cytokines induced by ET-1 was different in monocytes and macrophages, although an early increase in TNF-α was observed in both monocyte and macrophage supernatants. In conclusion, ET-1 stimulates monocytes and macrophages to release cytokines thereby demonstrating a potential role for ET-1 in regulation of inflammatory responses. Hindawi Publishing Corporation 1993 /pmc/articles/PMC2365438/ /pubmed/18475557 http://dx.doi.org/10.1155/S0962935193000596 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
Helset, E.
Sildnes, T.
Seljelid, R.
Konopski, Z.S.
Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6
title Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6
title_full Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6
title_fullStr Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6
title_full_unstemmed Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6
title_short Endothelin-1 stimulates human monocytes in vitro to release TNF-α , IL-1β and IL-6
title_sort endothelin-1 stimulates human monocytes in vitro to release tnf-α , il-1β and il-6
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365438/
https://www.ncbi.nlm.nih.gov/pubmed/18475557
http://dx.doi.org/10.1155/S0962935193000596
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