Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cells

Cyclosporin A (CsA) is an immunosuppresor drug that has been used in the treatment of several types of inflammatory diseases. In some of them the inhibition of T-lymphocyte activation does not suitably account for the observed beneficial effect, suggesting that CsA could act on other types of cells....

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Main Authors: Juan E. Losa Garcia, María Rosa Martín de Cabo, Fernando Mateos Rodríguez, Jesús Pérez Losada, Antonio Jiménez López, José Luis Pérez Arellano
Format: Article
Language:English
Published: Wiley 2000-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1080/09629350020008682
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author Juan E. Losa Garcia
María Rosa Martín de Cabo
Fernando Mateos Rodríguez
Jesús Pérez Losada
Antonio Jiménez López
José Luis Pérez Arellano
author_facet Juan E. Losa Garcia
María Rosa Martín de Cabo
Fernando Mateos Rodríguez
Jesús Pérez Losada
Antonio Jiménez López
José Luis Pérez Arellano
author_sort Juan E. Losa Garcia
collection DOAJ
description Cyclosporin A (CsA) is an immunosuppresor drug that has been used in the treatment of several types of inflammatory diseases. In some of them the inhibition of T-lymphocyte activation does not suitably account for the observed beneficial effect, suggesting that CsA could act on other types of cells. The present study was undertaken to determine the effect of CsA on inflammatory cytokine secretion by U937 monocyte cells. Undifferentiated and dimethylsulfoxide (DMSO) differentiated U937 cells were incubated with different concentrations of CsA (200, 20 and 2 ng/mL) in the presence or absence of phorbol-myristateacetate (PMA). Interleukin-1g (IL-1β), tumor necrosis factor-α (TNF-α), IL-6 and IL-8 levels were measured in supernatants using specific enzyme-linked immunosorbent assays. At the highest concentration used (200 ng/mL) CsA decreased the basal and stimulated secretion of all the inflammatory cytokines studied in both undifferentiated and differentiated cells, with the only exception of PMA-stim ulated IL-1 secretion by undifferentiated cells. However, only basal secretion of interleukin-8 in both undifferentiated and DMSO-differentiated U937 cells was significantly reduced by CsA at the highest concentration (200 ng/ mL). At therapeutic concentrations in vivo, CsA exerts a predominant effect on IL-8 secretion by human mononuclear phagocytes.
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spelling doaj-art-59e9192fdf1a42ee96d200920fe881212025-02-03T01:23:24ZengWileyMediators of Inflammation0962-93511466-18612000-01-0193-416917410.1080/09629350020008682Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cellsJuan E. Losa Garcia0María Rosa Martín de Cabo1Fernando Mateos Rodríguez2Jesús Pérez Losada3Antonio Jiménez López4José Luis Pérez Arellano5Fundación Hospital de Alcorcón, Alcorcón, SpainCentro de Salud Miguel Servet, Alcorcón, SpainHospital General de Albacete, Albacete, SpainUniversidad de Salamanca, Salamanca, SpainUniversidad de Salamanca, Salamanca, SpainDepartamento de Ciencias Clínicas, Universidad de Las Palmas, Las Palmas, SpainCyclosporin A (CsA) is an immunosuppresor drug that has been used in the treatment of several types of inflammatory diseases. In some of them the inhibition of T-lymphocyte activation does not suitably account for the observed beneficial effect, suggesting that CsA could act on other types of cells. The present study was undertaken to determine the effect of CsA on inflammatory cytokine secretion by U937 monocyte cells. Undifferentiated and dimethylsulfoxide (DMSO) differentiated U937 cells were incubated with different concentrations of CsA (200, 20 and 2 ng/mL) in the presence or absence of phorbol-myristateacetate (PMA). Interleukin-1g (IL-1β), tumor necrosis factor-α (TNF-α), IL-6 and IL-8 levels were measured in supernatants using specific enzyme-linked immunosorbent assays. At the highest concentration used (200 ng/mL) CsA decreased the basal and stimulated secretion of all the inflammatory cytokines studied in both undifferentiated and differentiated cells, with the only exception of PMA-stim ulated IL-1 secretion by undifferentiated cells. However, only basal secretion of interleukin-8 in both undifferentiated and DMSO-differentiated U937 cells was significantly reduced by CsA at the highest concentration (200 ng/ mL). At therapeutic concentrations in vivo, CsA exerts a predominant effect on IL-8 secretion by human mononuclear phagocytes.http://dx.doi.org/10.1080/09629350020008682
spellingShingle Juan E. Losa Garcia
María Rosa Martín de Cabo
Fernando Mateos Rodríguez
Jesús Pérez Losada
Antonio Jiménez López
José Luis Pérez Arellano
Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cells
Mediators of Inflammation
title Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cells
title_full Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cells
title_fullStr Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cells
title_full_unstemmed Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cells
title_short Effect of cyclosporin A on inflammatory cytokine production by U937 monocyte-like cells
title_sort effect of cyclosporin a on inflammatory cytokine production by u937 monocyte like cells
url http://dx.doi.org/10.1080/09629350020008682
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