Human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release

Abstract Background β2-adrenoceptor agonists have been shown to reduce the lipopolysaccharide (LPS)-induced cytokine release by human monocyte-derived macrophages (MDMs). We compare the expression of β2-adrenoceptors and the inhibitory effect of formoterol and salmeterol on the LPS-induced release o...

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Main Authors: Tatiana Victoni, Hélène Salvator, Charlotte Abrial, Marion Brollo, Luis Cristovão Sobrino Porto, Vincent Lagente, Emmanuel Naline, Stanislas Grassin-Delyle, Philippe Devillier
Format: Article
Language:English
Published: BioMed Central 2017-06-01
Series:Respiratory Research
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12931-017-0613-y
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spelling doaj-art-ee563f613beb4309b150535514c40dfa2018-08-15T23:45:35ZengBioMed CentralRespiratory Research1465-993X2017-06-0118111010.1186/s12931-017-0613-yHuman lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine releaseTatiana Victoni0Hélène Salvator1Charlotte Abrial2Marion Brollo3Luis Cristovão Sobrino Porto4Vincent Lagente5Emmanuel Naline6Stanislas Grassin-Delyle7Philippe Devillier8Laboratory of Histocompatibility and Cryopresevation, Laboratory of Tissue RepairLaboratory of Research in Respiratory Pharmacology–UPRES EA220, UFR Sciences de la Santé Simone Veil, Université Versailles Saint-Quentin, Université Paris-SaclayLaboratory of Research in Respiratory Pharmacology–UPRES EA220, UFR Sciences de la Santé Simone Veil, Université Versailles Saint-Quentin, Université Paris-SaclayLaboratory of Research in Respiratory Pharmacology–UPRES EA220, UFR Sciences de la Santé Simone Veil, Université Versailles Saint-Quentin, Université Paris-SaclayLaboratory of Histocompatibility and Cryopresevation, Laboratory of Tissue RepairNutrition Metabolisms and Cancer, INSERM, INRA, Université Rennes 1, Université Bretagne LoireLaboratory of Research in Respiratory Pharmacology–UPRES EA220, UFR Sciences de la Santé Simone Veil, Université Versailles Saint-Quentin, Université Paris-SaclayDepartment of Airway Diseases, Foch HospitalLaboratory of Research in Respiratory Pharmacology–UPRES EA220, UFR Sciences de la Santé Simone Veil, Université Versailles Saint-Quentin, Université Paris-SaclayAbstract Background β2-adrenoceptor agonists have been shown to reduce the lipopolysaccharide (LPS)-induced cytokine release by human monocyte-derived macrophages (MDMs). We compare the expression of β2-adrenoceptors and the inhibitory effect of formoterol and salmeterol on the LPS-induced release of tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6 and a range of chemokines (CCL2, 3, 4, and IL-8) by human lung macrophages (LMs) and MDMs. Methods LMs were isolated from patients undergoing resection and MDMs were obtained from blood monocytes in the presence of GM-CSF. LMs and MDMs were incubated in the absence or presence of formoterol or salmeterol prior to stimulation with LPS. The effects of formoterol were also assessed in the presence of the phosphodiesterase inhibitor roflumilast. Results LPS-induced cytokine production was higher in LMs than in MDMs. Salmeterol and formoterol exerted an inhibitory effect on the LPS-induced production of TNF-α, IL-6, CCL2, CCL3, and CCL4 in MDMs. In contrast, the β2-adrenoceptor agonists were devoid of any effect on LMs - even in the presence of roflumilast. The expression of β2-adrenergic receptors was detected on Western blots in MDMs but not in LMs. Conclusions Concentrations of β2-adrenoceptor agonists that cause relaxation of the human bronchus can inhibit cytokine production by LPS-stimulated MDMs but not by LMs.http://link.springer.com/article/10.1186/s12931-017-0613-yβ2-adrenoceptorCytokinesLipopolysaccharideLung macrophageMonocyte-derived macrophage
institution Open Data Bank
collection Open Access Journals
building Directory of Open Access Journals
language English
format Article
author Tatiana Victoni
Hélène Salvator
Charlotte Abrial
Marion Brollo
Luis Cristovão Sobrino Porto
Vincent Lagente
Emmanuel Naline
Stanislas Grassin-Delyle
Philippe Devillier
spellingShingle Tatiana Victoni
Hélène Salvator
Charlotte Abrial
Marion Brollo
Luis Cristovão Sobrino Porto
Vincent Lagente
Emmanuel Naline
Stanislas Grassin-Delyle
Philippe Devillier
Human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release
Respiratory Research
β2-adrenoceptor
Cytokines
Lipopolysaccharide
Lung macrophage
Monocyte-derived macrophage
author_facet Tatiana Victoni
Hélène Salvator
Charlotte Abrial
Marion Brollo
Luis Cristovão Sobrino Porto
Vincent Lagente
Emmanuel Naline
Stanislas Grassin-Delyle
Philippe Devillier
author_sort Tatiana Victoni
title Human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release
title_short Human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release
title_full Human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release
title_fullStr Human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release
title_full_unstemmed Human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release
title_sort human lung and monocyte-derived macrophages differ with regard to the effects of β2-adrenoceptor agonists on cytokine release
publisher BioMed Central
series Respiratory Research
issn 1465-993X
publishDate 2017-06-01
description Abstract Background β2-adrenoceptor agonists have been shown to reduce the lipopolysaccharide (LPS)-induced cytokine release by human monocyte-derived macrophages (MDMs). We compare the expression of β2-adrenoceptors and the inhibitory effect of formoterol and salmeterol on the LPS-induced release of tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6 and a range of chemokines (CCL2, 3, 4, and IL-8) by human lung macrophages (LMs) and MDMs. Methods LMs were isolated from patients undergoing resection and MDMs were obtained from blood monocytes in the presence of GM-CSF. LMs and MDMs were incubated in the absence or presence of formoterol or salmeterol prior to stimulation with LPS. The effects of formoterol were also assessed in the presence of the phosphodiesterase inhibitor roflumilast. Results LPS-induced cytokine production was higher in LMs than in MDMs. Salmeterol and formoterol exerted an inhibitory effect on the LPS-induced production of TNF-α, IL-6, CCL2, CCL3, and CCL4 in MDMs. In contrast, the β2-adrenoceptor agonists were devoid of any effect on LMs - even in the presence of roflumilast. The expression of β2-adrenergic receptors was detected on Western blots in MDMs but not in LMs. Conclusions Concentrations of β2-adrenoceptor agonists that cause relaxation of the human bronchus can inhibit cytokine production by LPS-stimulated MDMs but not by LMs.
topic β2-adrenoceptor
Cytokines
Lipopolysaccharide
Lung macrophage
Monocyte-derived macrophage
url http://link.springer.com/article/10.1186/s12931-017-0613-y
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