Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type

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Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type. / van der Plas, Mariena J A; van Dissel, Jaap T; Nibbering, Peter H.

In: PLOS ONE, Vol. 4, No. 11, 30.11.2009, p. e8071.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

van der Plas, MJA, van Dissel, JT & Nibbering, PH 2009, 'Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type', PLOS ONE, vol. 4, no. 11, pp. e8071. https://doi.org/10.1371/journal.pone.0008071

APA

van der Plas, M. J. A., van Dissel, J. T., & Nibbering, P. H. (2009). Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type. PLOS ONE, 4(11), e8071. https://doi.org/10.1371/journal.pone.0008071

Vancouver

van der Plas MJA, van Dissel JT, Nibbering PH. Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type. PLOS ONE. 2009 Nov 30;4(11):e8071. https://doi.org/10.1371/journal.pone.0008071

Author

van der Plas, Mariena J A ; van Dissel, Jaap T ; Nibbering, Peter H. / Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type. In: PLOS ONE. 2009 ; Vol. 4, No. 11. pp. e8071.

Bibtex

@article{01f1e543dcbe4042ba95adb757dc70e7,
title = "Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type",
abstract = "BACKGROUND: Maggots of the blowfly Lucilia sericata are used for the treatment of chronic wounds. Earlier we reported maggot secretions to inhibit pro-inflammatory responses of human monocytes. The aim of this study was to investigate the effect of maggot secretions on the differentiation of monocytes into pro-inflammatory (M{\O}-1) and anti-inflammatory/pro-angiogenic macrophages (M{\O}-2) as these cells play a central role in wound healing.METHODOLOGY/PRINCIPAL FINDINGS: Freshly isolated monocytes were incubated with secretions and GM-CSF or M-CSF for 6 days and then stimulated with LPS or LTA for 18 h. The expression of cell surface molecules and the levels of cytokines, chemokines and growth factors in supernatants were measured. Our results showed secretions to affect monocyte-macrophage differentiation leading to M{\O}-1 with a partial M{\O}-2-like morphology but lacking CD163, which is characteristic for M{\O}-2. In response to LPS or LTA, secretions-differentiated M{\O}-1 produced less pro-inflammatory cytokines (TNF-alpha, IL-12p40 and MIF) than control cells. Similar results were observed for M{\O}-2 when stimulated with low concentrations of LPS. Furthermore, secretions dose-dependently led to M{\O}-1 and M{\O}-2 characterized by an altered chemokine production. Secretions led to M{\O}-2, but not M{\O}-1, producing enhanced levels of the growth factors bFGF and VEGF, as compared to control cells. The expression of cell-surface receptors involved in LPS/LTA was enhanced by secretions, that of CD86 and HLA-DR down-regulated, while receptors involved in phagocytosis remained largely unaffected.CONCLUSIONS: Maggot secretions skew the differentiation of monocytes into macrophages away from a pro-inflammatory to a pro-angiogenic type.",
keywords = "Animals, Cell Differentiation, Cytokines, Diptera, Flow Cytometry, Humans, Inflammation, Larva, Lipopolysaccharides, Lymphocytes, Macrophages, Monocytes, Neovascularization, Pathologic, Wound Healing, Journal Article, Research Support, Non-U.S. Gov't",
author = "{van der Plas}, {Mariena J A} and {van Dissel}, {Jaap T} and Nibbering, {Peter H}",
year = "2009",
month = nov,
day = "30",
doi = "10.1371/journal.pone.0008071",
language = "English",
volume = "4",
pages = "e8071",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "11",

}

RIS

TY - JOUR

T1 - Maggot secretions skew monocyte-macrophage differentiation away from a pro-inflammatory to a pro-angiogenic type

AU - van der Plas, Mariena J A

AU - van Dissel, Jaap T

AU - Nibbering, Peter H

PY - 2009/11/30

Y1 - 2009/11/30

N2 - BACKGROUND: Maggots of the blowfly Lucilia sericata are used for the treatment of chronic wounds. Earlier we reported maggot secretions to inhibit pro-inflammatory responses of human monocytes. The aim of this study was to investigate the effect of maggot secretions on the differentiation of monocytes into pro-inflammatory (MØ-1) and anti-inflammatory/pro-angiogenic macrophages (MØ-2) as these cells play a central role in wound healing.METHODOLOGY/PRINCIPAL FINDINGS: Freshly isolated monocytes were incubated with secretions and GM-CSF or M-CSF for 6 days and then stimulated with LPS or LTA for 18 h. The expression of cell surface molecules and the levels of cytokines, chemokines and growth factors in supernatants were measured. Our results showed secretions to affect monocyte-macrophage differentiation leading to MØ-1 with a partial MØ-2-like morphology but lacking CD163, which is characteristic for MØ-2. In response to LPS or LTA, secretions-differentiated MØ-1 produced less pro-inflammatory cytokines (TNF-alpha, IL-12p40 and MIF) than control cells. Similar results were observed for MØ-2 when stimulated with low concentrations of LPS. Furthermore, secretions dose-dependently led to MØ-1 and MØ-2 characterized by an altered chemokine production. Secretions led to MØ-2, but not MØ-1, producing enhanced levels of the growth factors bFGF and VEGF, as compared to control cells. The expression of cell-surface receptors involved in LPS/LTA was enhanced by secretions, that of CD86 and HLA-DR down-regulated, while receptors involved in phagocytosis remained largely unaffected.CONCLUSIONS: Maggot secretions skew the differentiation of monocytes into macrophages away from a pro-inflammatory to a pro-angiogenic type.

AB - BACKGROUND: Maggots of the blowfly Lucilia sericata are used for the treatment of chronic wounds. Earlier we reported maggot secretions to inhibit pro-inflammatory responses of human monocytes. The aim of this study was to investigate the effect of maggot secretions on the differentiation of monocytes into pro-inflammatory (MØ-1) and anti-inflammatory/pro-angiogenic macrophages (MØ-2) as these cells play a central role in wound healing.METHODOLOGY/PRINCIPAL FINDINGS: Freshly isolated monocytes were incubated with secretions and GM-CSF or M-CSF for 6 days and then stimulated with LPS or LTA for 18 h. The expression of cell surface molecules and the levels of cytokines, chemokines and growth factors in supernatants were measured. Our results showed secretions to affect monocyte-macrophage differentiation leading to MØ-1 with a partial MØ-2-like morphology but lacking CD163, which is characteristic for MØ-2. In response to LPS or LTA, secretions-differentiated MØ-1 produced less pro-inflammatory cytokines (TNF-alpha, IL-12p40 and MIF) than control cells. Similar results were observed for MØ-2 when stimulated with low concentrations of LPS. Furthermore, secretions dose-dependently led to MØ-1 and MØ-2 characterized by an altered chemokine production. Secretions led to MØ-2, but not MØ-1, producing enhanced levels of the growth factors bFGF and VEGF, as compared to control cells. The expression of cell-surface receptors involved in LPS/LTA was enhanced by secretions, that of CD86 and HLA-DR down-regulated, while receptors involved in phagocytosis remained largely unaffected.CONCLUSIONS: Maggot secretions skew the differentiation of monocytes into macrophages away from a pro-inflammatory to a pro-angiogenic type.

KW - Animals

KW - Cell Differentiation

KW - Cytokines

KW - Diptera

KW - Flow Cytometry

KW - Humans

KW - Inflammation

KW - Larva

KW - Lipopolysaccharides

KW - Lymphocytes

KW - Macrophages

KW - Monocytes

KW - Neovascularization, Pathologic

KW - Wound Healing

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.1371/journal.pone.0008071

DO - 10.1371/journal.pone.0008071

M3 - Journal article

C2 - 19956650

VL - 4

SP - e8071

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 11

ER -

ID: 186451203