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Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma

BACKGROUND: Galectin-3 is a 32 kDa protein secreted by macrophages involved in processes such as cell activation, chemotaxis and phagocytosis. Galectin-3 has previously been shown to improve the ability of airway macrophages to ingest apoptotic cells (efferocytosis) in chronic obstructive pulmonary...

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Autores principales: Erriah, Melanie, Pabreja, Kavita, Fricker, Michael, Baines, Katherine J., Donnelly, Louise E., Bylund, Johan, Karlsson, Anna, Simpson, Jodie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318889/
https://www.ncbi.nlm.nih.gov/pubmed/30606211
http://dx.doi.org/10.1186/s12931-018-0967-9
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author Erriah, Melanie
Pabreja, Kavita
Fricker, Michael
Baines, Katherine J.
Donnelly, Louise E.
Bylund, Johan
Karlsson, Anna
Simpson, Jodie L.
author_facet Erriah, Melanie
Pabreja, Kavita
Fricker, Michael
Baines, Katherine J.
Donnelly, Louise E.
Bylund, Johan
Karlsson, Anna
Simpson, Jodie L.
author_sort Erriah, Melanie
collection PubMed
description BACKGROUND: Galectin-3 is a 32 kDa protein secreted by macrophages involved in processes such as cell activation, chemotaxis and phagocytosis. Galectin-3 has previously been shown to improve the ability of airway macrophages to ingest apoptotic cells (efferocytosis) in chronic obstructive pulmonary disease (COPD) and may be of interest in non-eosinophilic asthma (NEA) which is also characterised by impaired efferocytosis. It was hypothesised that the addition of exogenous galectin-3 to monocyte-derived macrophages (MDMs) derived from donors with NEA would enhance their ability to engulf apoptotic granulocytes. METHODS: Eligible non-smoking adults with asthma (n = 19), including 7 with NEA and healthy controls (n = 10) underwent a clinical assessment, venepuncture and sputum induction. MDMs were co-cultured with apoptotic granulocytes isolated from healthy donors with or without exogenous recombinant galectin-3 (50 μg/mL) and efferocytosis was assessed by flow cytometry. Galectin-3 expression and localisation in MDMs was visualised by immunofluorescence staining and fluorescence microscopy. Galectin-3, interleukin (IL)-6 and CXCL8 secretion were measured in cell culture supernatants by ELISA and cytometric bead array. RESULTS: Baseline efferocytosis (mean (±standard deviation)) was lower in participants with asthma (33.2 (±17.7)%) compared with healthy controls (45.3 (±15.9)%; p = 0.081). Efferocytosis did not differ between the participants with eosinophilic asthma (EA) (31.4 (±19.2)%) and NEA (28.7 (±21.5)%; p = 0.748). Addition of galectin-3 significantly improved efferocytosis in asthma, particularly in NEA (37.8 (±18.1)%) compared with baseline (30.4 (±19.7)%; p = 0.012). Efferocytosis was not associated with any of the clinical outcomes but was negatively correlated with sputum macrophage numbers (Spearman r = − 0.671; p = 0.017). Galectin-3 was diffusely distributed in most MDMs but formed punctate structures in 5% of MDMs. MDM galectin-3 secretion was lower in asthma (9.99 (2.67, 15.48) ng/mL) compared with the healthy controls (20.72 (11.28, 27.89) ng/mL; p = 0.044) while IL-6 and CXCL8 levels were similar. CONCLUSIONS: Galectin-3 modulates macrophage function in asthma, indicating a potential role for galectin-3 to reverse impaired efferocytosis in NEA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0967-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-63188892019-01-08 Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma Erriah, Melanie Pabreja, Kavita Fricker, Michael Baines, Katherine J. Donnelly, Louise E. Bylund, Johan Karlsson, Anna Simpson, Jodie L. Respir Res Research BACKGROUND: Galectin-3 is a 32 kDa protein secreted by macrophages involved in processes such as cell activation, chemotaxis and phagocytosis. Galectin-3 has previously been shown to improve the ability of airway macrophages to ingest apoptotic cells (efferocytosis) in chronic obstructive pulmonary disease (COPD) and may be of interest in non-eosinophilic asthma (NEA) which is also characterised by impaired efferocytosis. It was hypothesised that the addition of exogenous galectin-3 to monocyte-derived macrophages (MDMs) derived from donors with NEA would enhance their ability to engulf apoptotic granulocytes. METHODS: Eligible non-smoking adults with asthma (n = 19), including 7 with NEA and healthy controls (n = 10) underwent a clinical assessment, venepuncture and sputum induction. MDMs were co-cultured with apoptotic granulocytes isolated from healthy donors with or without exogenous recombinant galectin-3 (50 μg/mL) and efferocytosis was assessed by flow cytometry. Galectin-3 expression and localisation in MDMs was visualised by immunofluorescence staining and fluorescence microscopy. Galectin-3, interleukin (IL)-6 and CXCL8 secretion were measured in cell culture supernatants by ELISA and cytometric bead array. RESULTS: Baseline efferocytosis (mean (±standard deviation)) was lower in participants with asthma (33.2 (±17.7)%) compared with healthy controls (45.3 (±15.9)%; p = 0.081). Efferocytosis did not differ between the participants with eosinophilic asthma (EA) (31.4 (±19.2)%) and NEA (28.7 (±21.5)%; p = 0.748). Addition of galectin-3 significantly improved efferocytosis in asthma, particularly in NEA (37.8 (±18.1)%) compared with baseline (30.4 (±19.7)%; p = 0.012). Efferocytosis was not associated with any of the clinical outcomes but was negatively correlated with sputum macrophage numbers (Spearman r = − 0.671; p = 0.017). Galectin-3 was diffusely distributed in most MDMs but formed punctate structures in 5% of MDMs. MDM galectin-3 secretion was lower in asthma (9.99 (2.67, 15.48) ng/mL) compared with the healthy controls (20.72 (11.28, 27.89) ng/mL; p = 0.044) while IL-6 and CXCL8 levels were similar. CONCLUSIONS: Galectin-3 modulates macrophage function in asthma, indicating a potential role for galectin-3 to reverse impaired efferocytosis in NEA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0967-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-03 2019 /pmc/articles/PMC6318889/ /pubmed/30606211 http://dx.doi.org/10.1186/s12931-018-0967-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Erriah, Melanie
Pabreja, Kavita
Fricker, Michael
Baines, Katherine J.
Donnelly, Louise E.
Bylund, Johan
Karlsson, Anna
Simpson, Jodie L.
Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma
title Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma
title_full Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma
title_fullStr Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma
title_full_unstemmed Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma
title_short Galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma
title_sort galectin-3 enhances monocyte-derived macrophage efferocytosis of apoptotic granulocytes in asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318889/
https://www.ncbi.nlm.nih.gov/pubmed/30606211
http://dx.doi.org/10.1186/s12931-018-0967-9
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