G-CSF and GM-CSF Modify Neutrophil Functions at Concentrations found in Cystic Fibrosis
The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has not been thoroughly evaluated, considering that the neutrophil burden of lung inflammation in these subjects is very high. The aim of this study was to assess granulocyte-CSF (G-CSF) and granulocyte-mac...
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Published in | Scientific reports Vol. 9; no. 1; pp. 12937 - 11 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
10.09.2019
Nature Publishing Group |
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Online Access | Get full text |
ISSN | 2045-2322 2045-2322 |
DOI | 10.1038/s41598-019-49419-z |
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Abstract | The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has not been thoroughly evaluated, considering that the neutrophil burden of lung inflammation in these subjects is very high. The aim of this study was to assess granulocyte-CSF (G-CSF) and granulocyte-macrophage-CSF (GM-CSF) levels in CF patients in various clinical conditions and how these cytokines impact on activation and priming of neutrophils. G-CSF and GM-CSF levels were measured in sputum and serum samples of stable CF patients (n = 21) and in CF patients with acute exacerbation before and after a course of antibiotic therapy (n = 19). CSFs were tested on non CF neutrophils to investigate their effects on reactive oxygen species (ROS) production, degranulation (CD66b, elastase, lactoferrin, MMP-9), and chemotaxis. At very low concentrations found in CF patients (0.005–0.1 ng/ml), both cytokines inhibited ROS production, while higher concentrations (1–5 ng/ml) exerted a stimulatory effect. While either CSF induced elastase and MMP-9 secretion, lactoferrin levels were increased only by G-CSF. Chemotaxis was inhibited by GM-CSF, but was increased by G-CSF. However, when present together at low concentrations, CSFs increased basal and fMLP-stimulated ROS production and chemotaxis. These results suggest the CSF levels that circulating neutrophils face before extravasating into the lungs of CF patients may enhance their function contributing to the airway damage. |
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AbstractList | The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has not been thoroughly evaluated, considering that the neutrophil burden of lung inflammation in these subjects is very high. The aim of this study was to assess granulocyte-CSF (G-CSF) and granulocyte-macrophage-CSF (GM-CSF) levels in CF patients in various clinical conditions and how these cytokines impact on activation and priming of neutrophils. G-CSF and GM-CSF levels were measured in sputum and serum samples of stable CF patients (n = 21) and in CF patients with acute exacerbation before and after a course of antibiotic therapy (n = 19). CSFs were tested on non CF neutrophils to investigate their effects on reactive oxygen species (ROS) production, degranulation (CD66b, elastase, lactoferrin, MMP-9), and chemotaxis. At very low concentrations found in CF patients (0.005–0.1 ng/ml), both cytokines inhibited ROS production, while higher concentrations (1–5 ng/ml) exerted a stimulatory effect. While either CSF induced elastase and MMP-9 secretion, lactoferrin levels were increased only by G-CSF. Chemotaxis was inhibited by GM-CSF, but was increased by G-CSF. However, when present together at low concentrations, CSFs increased basal and fMLP-stimulated ROS production and chemotaxis. These results suggest the CSF levels that circulating neutrophils face before extravasating into the lungs of CF patients may enhance their function contributing to the airway damage. The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has not been thoroughly evaluated, considering that the neutrophil burden of lung inflammation in these subjects is very high. The aim of this study was to assess granulocyte-CSF (G-CSF) and granulocyte-macrophage-CSF (GM-CSF) levels in CF patients in various clinical conditions and how these cytokines impact on activation and priming of neutrophils. G-CSF and GM-CSF levels were measured in sputum and serum samples of stable CF patients (n = 21) and in CF patients with acute exacerbation before and after a course of antibiotic therapy (n = 19). CSFs were tested on non CF neutrophils to investigate their effects on reactive oxygen species (ROS) production, degranulation (CD66b, elastase, lactoferrin, MMP-9), and chemotaxis. At very low concentrations found in CF patients (0.005-0.1 ng/ml), both cytokines inhibited ROS production, while higher concentrations (1-5 ng/ml) exerted a stimulatory effect. While either CSF induced elastase and MMP-9 secretion, lactoferrin levels were increased only by G-CSF. Chemotaxis was inhibited by GM-CSF, but was increased by G-CSF. However, when present together at low concentrations, CSFs increased basal and fMLP-stimulated ROS production and chemotaxis. These results suggest the CSF levels that circulating neutrophils face before extravasating into the lungs of CF patients may enhance their function contributing to the airway damage.The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has not been thoroughly evaluated, considering that the neutrophil burden of lung inflammation in these subjects is very high. The aim of this study was to assess granulocyte-CSF (G-CSF) and granulocyte-macrophage-CSF (GM-CSF) levels in CF patients in various clinical conditions and how these cytokines impact on activation and priming of neutrophils. G-CSF and GM-CSF levels were measured in sputum and serum samples of stable CF patients (n = 21) and in CF patients with acute exacerbation before and after a course of antibiotic therapy (n = 19). CSFs were tested on non CF neutrophils to investigate their effects on reactive oxygen species (ROS) production, degranulation (CD66b, elastase, lactoferrin, MMP-9), and chemotaxis. At very low concentrations found in CF patients (0.005-0.1 ng/ml), both cytokines inhibited ROS production, while higher concentrations (1-5 ng/ml) exerted a stimulatory effect. While either CSF induced elastase and MMP-9 secretion, lactoferrin levels were increased only by G-CSF. Chemotaxis was inhibited by GM-CSF, but was increased by G-CSF. However, when present together at low concentrations, CSFs increased basal and fMLP-stimulated ROS production and chemotaxis. These results suggest the CSF levels that circulating neutrophils face before extravasating into the lungs of CF patients may enhance their function contributing to the airway damage. |
ArticleNumber | 12937 |
Author | Mariggiò, Maria Addolorata Gallo, Crescenzio Diana, Anna Polizzi, Angela Maria Conese, Massimo Di Gioia, Sante De Venuto, Domenica D’Oria, Susanna Vinella, Angela Leonetti, Giuseppina Castellani, Stefano Guerra, Lorenzo Montemurro, Pasqualina Favia, Maria |
Author_xml | – sequence: 1 givenname: Stefano surname: Castellani fullname: Castellani, Stefano organization: Department of Medical and Surgical Sciences, University of Foggia – sequence: 2 givenname: Susanna surname: D’Oria fullname: D’Oria, Susanna organization: Department of Biomedical Sciences and Human Oncology, Section of General Pathology, University of Bari – sequence: 3 givenname: Anna surname: Diana fullname: Diana, Anna organization: Department of Biomedical Sciences and Human Oncology, Section of Medical Genetics, University of Bari – sequence: 4 givenname: Angela Maria surname: Polizzi fullname: Polizzi, Angela Maria organization: Department of Biomedical Sciences and Human Oncology, Section of Medical Genetics, University of Bari – sequence: 5 givenname: Sante surname: Di Gioia fullname: Di Gioia, Sante organization: Department of Medical and Surgical Sciences, University of Foggia – sequence: 6 givenname: Maria Addolorata surname: Mariggiò fullname: Mariggiò, Maria Addolorata organization: Department of Biomedical Sciences and Human Oncology, Section of General Pathology, University of Bari – sequence: 7 givenname: Lorenzo surname: Guerra fullname: Guerra, Lorenzo organization: Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari – sequence: 8 givenname: Maria surname: Favia fullname: Favia, Maria organization: Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari – sequence: 9 givenname: Angela surname: Vinella fullname: Vinella, Angela organization: Department of Biomedical Sciences and Human Oncology, Section of General Pathology, University of Bari – sequence: 10 givenname: Giuseppina surname: Leonetti fullname: Leonetti, Giuseppina organization: Cystic Fibrosis Regional Center, Department of Biomedical and Human Oncology, Pediatrics Section, U.O. “B. Trambusti”, Policlinico, University of Bari – sequence: 11 givenname: Domenica surname: De Venuto fullname: De Venuto, Domenica organization: Cystic Fibrosis Regional Center, Department of Biomedical and Human Oncology, Pediatrics Section, U.O. “B. Trambusti”, Policlinico, University of Bari – sequence: 12 givenname: Crescenzio orcidid: 0000-0002-3929-462X surname: Gallo fullname: Gallo, Crescenzio organization: Department of Clinical and Experimental Medicine, University of Foggia – sequence: 13 givenname: Pasqualina surname: Montemurro fullname: Montemurro, Pasqualina email: pasqualina.montemurro@uniba.it organization: Department of Biomedical Sciences and Human Oncology, Section of General Pathology, University of Bari – sequence: 14 givenname: Massimo orcidid: 0000-0003-3465-6641 surname: Conese fullname: Conese, Massimo email: massimo.conese@unifg.it organization: Department of Medical and Surgical Sciences, University of Foggia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31506515$$D View this record in MEDLINE/PubMed |
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Title | G-CSF and GM-CSF Modify Neutrophil Functions at Concentrations found in Cystic Fibrosis |
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