Peripheral Neutrophil Functions and Cell Signalling in Crohn`s Disease

The role of the innate immunity in the pathogenesis of Crohn's disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils (PMN) are key members of the innate immune system which migrate to sites of bacterial infection and initiate the defence against microbes...

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Published inPloS one Vol. 8; no. 12; p. e84521
Main Authors Somasundaram, Rajesh, Nuij, Veerle J. A. A., van der Woude, C. Janneke, Kuipers, Ernst J., Peppelenbosch, Maikel P., Fuhler, Gwenny M.
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 19.12.2013
Public Library of Science (PLoS)
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Online AccessGet full text
ISSN1932-6203
1932-6203
DOI10.1371/journal.pone.0084521

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Abstract The role of the innate immunity in the pathogenesis of Crohn's disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils (PMN) are key members of the innate immune system which migrate to sites of bacterial infection and initiate the defence against microbes by producing reactive oxygen species (ROS), before undergoing apoptosis. It is believed that impaired innate immune responses contribute to CD, but it is as yet unclear whether intrinsic defects in PMN signal transduction and corresponding function are present in patients with quiescent disease. We isolated peripheral blood PMN from CD patients in remission and healthy controls (HC), and characterised migration, bacterial uptake and killing, ROS production and cell death signalling. Whereas IL8-induced migration and signalling were normal in CD, trans-epithelial migration was significantly impaired. Uptake and killing of E. coli were normal. However, an increased ROS production was observed in CD PMN after stimulation with the bacterial peptide analogue fMLP, which was mirrored by an increased fMLP-triggered ERK and AKT signal activation. Interestingly, cleavage of caspase-3 and caspase-8 during GMCSF-induced rescue from cell-death was decreased in CD neutrophils, but a reduced survival signal emanating from STAT3 and AKT pathways was concomitantly observed, resulting in a similar percentage of end stage apoptotic PMN in CD patients and HC. In toto, these data show a disturbed signal transduction activation and functionality in peripheral blood PMN from patients with quiescent CD, which point toward an intrinsic defect in innate immunity in these patients.
AbstractList The role of the innate immunity in the pathogenesis of Crohn's disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils (PMN) are key members of the innate immune system which migrate to sites of bacterial infection and initiate the defence against microbes by producing reactive oxygen species (ROS), before undergoing apoptosis. It is believed that impaired innate immune responses contribute to CD, but it is as yet unclear whether intrinsic defects in PMN signal transduction and corresponding function are present in patients with quiescent disease. We isolated peripheral blood PMN from CD patients in remission and healthy controls (HC), and characterised migration, bacterial uptake and killing, ROS production and cell death signalling. Whereas IL8-induced migration and signalling were normal in CD, trans-epithelial migration was significantly impaired. Uptake and killing of E. coli were normal. However, an increased ROS production was observed in CD PMN after stimulation with the bacterial peptide analogue fMLP, which was mirrored by an increased fMLP-triggered ERK and AKT signal activation. Interestingly, cleavage of caspase-3 and caspase-8 during GMCSF-induced rescue from cell-death was decreased in CD neutrophils, but a reduced survival signal emanating from STAT3 and AKT pathways was concomitantly observed, resulting in a similar percentage of end stage apoptotic PMN in CD patients and HC. In toto, these data show a disturbed signal transduction activation and functionality in peripheral blood PMN from patients with quiescent CD, which point toward an intrinsic defect in innate immunity in these patients.
The role of the innate immunity in the pathogenesis of Crohn’s disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils (PMN) are key members of the innate immune system which migrate to sites of bacterial infection and initiate the defence against microbes by producing reactive oxygen species (ROS), before undergoing apoptosis. It is believed that impaired innate immune responses contribute to CD, but it is as yet unclear whether intrinsic defects in PMN signal transduction and corresponding function are present in patients with quiescent disease. We isolated peripheral blood PMN from CD patients in remission and healthy controls (HC), and characterised migration, bacterial uptake and killing, ROS production and cell death signalling. Whereas IL8-induced migration and signalling were normal in CD, trans-epithelial migration was significantly impaired. Uptake and killing of E. coli were normal. However, an increased ROS production was observed in CD PMN after stimulation with the bacterial peptide analogue fMLP, which was mirrored by an increased fMLP-triggered ERK and AKT signal activation. Interestingly, cleavage of caspase-3 and caspase-8 during GMCSF-induced rescue from cell-death was decreased in CD neutrophils, but a reduced survival signal emanating from STAT3 and AKT pathways was concomitantly observed, resulting in a similar percentage of end stage apoptotic PMN in CD patients and HC. In toto , these data show a disturbed signal transduction activation and functionality in peripheral blood PMN from patients with quiescent CD, which point toward an intrinsic defect in innate immunity in these patients.
The role of the innate immunity in the pathogenesis of Crohn's disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils (PMN) are key members of the innate immune system which migrate to sites of bacterial infection and initiate the defence against microbes by producing reactive oxygen species (ROS), before undergoing apoptosis. It is believed that impaired innate immune responses contribute to CD, but it is as yet unclear whether intrinsic defects in PMN signal transduction and corresponding function are present in patients with quiescent disease. We isolated peripheral blood PMN from CD patients in remission and healthy controls (HC), and characterised migration, bacterial uptake and killing, ROS production and cell death signalling. Whereas IL8-induced migration and signalling were normal in CD, trans-epithelial migration was significantly impaired. Uptake and killing of E. coli were normal. However, an increased ROS production was observed in CD PMN after stimulation with the bacterial peptide analogue fMLP, which was mirrored by an increased fMLP-triggered ERK and AKT signal activation. Interestingly, cleavage of caspase-3 and caspase-8 during GMCSF-induced rescue from cell-death was decreased in CD neutrophils, but a reduced survival signal emanating from STAT3 and AKT pathways was concomitantly observed, resulting in a similar percentage of end stage apoptotic PMN in CD patients and HC. In toto, these data show a disturbed signal transduction activation and functionality in peripheral blood PMN from patients with quiescent CD, which point toward an intrinsic defect in innate immunity in these patients.The role of the innate immunity in the pathogenesis of Crohn's disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils (PMN) are key members of the innate immune system which migrate to sites of bacterial infection and initiate the defence against microbes by producing reactive oxygen species (ROS), before undergoing apoptosis. It is believed that impaired innate immune responses contribute to CD, but it is as yet unclear whether intrinsic defects in PMN signal transduction and corresponding function are present in patients with quiescent disease. We isolated peripheral blood PMN from CD patients in remission and healthy controls (HC), and characterised migration, bacterial uptake and killing, ROS production and cell death signalling. Whereas IL8-induced migration and signalling were normal in CD, trans-epithelial migration was significantly impaired. Uptake and killing of E. coli were normal. However, an increased ROS production was observed in CD PMN after stimulation with the bacterial peptide analogue fMLP, which was mirrored by an increased fMLP-triggered ERK and AKT signal activation. Interestingly, cleavage of caspase-3 and caspase-8 during GMCSF-induced rescue from cell-death was decreased in CD neutrophils, but a reduced survival signal emanating from STAT3 and AKT pathways was concomitantly observed, resulting in a similar percentage of end stage apoptotic PMN in CD patients and HC. In toto, these data show a disturbed signal transduction activation and functionality in peripheral blood PMN from patients with quiescent CD, which point toward an intrinsic defect in innate immunity in these patients.
Audience Academic
Author Kuipers, Ernst J.
Nuij, Veerle J. A. A.
Peppelenbosch, Maikel P.
van der Woude, C. Janneke
Fuhler, Gwenny M.
Somasundaram, Rajesh
AuthorAffiliation Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, Rotterdam, The Netherlands
University of San Francisco, United States of America
AuthorAffiliation_xml – name: University of San Francisco, United States of America
– name: Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, Rotterdam, The Netherlands
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/24367671$$D View this record in MEDLINE/PubMed
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2013 Somasundaram et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Conceived and designed the experiments: RS CJW EJK MPP GMF. Performed the experiments: RS VJJA GMF. Analyzed the data: RS VJJAN CJW MPP GMF. Wrote the manuscript: RS VJAAN MPP GMF.
Competing Interests: The authors have declared that no competing interests exist.
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Snippet The role of the innate immunity in the pathogenesis of Crohn's disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils...
The role of the innate immunity in the pathogenesis of Crohn’s disease (CD), an inflammatory bowel disease, is a subject of increasing interest. Neutrophils...
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StartPage e84521
SubjectTerms Activation
Adult
Aged
AKT protein
Apoptosis
Apoptosis - drug effects
Bacteria
Bacterial diseases
Bacterial infections
Binding sites
Blood
Caspase
Caspase-3
Caspase-8
Caspases - metabolism
Cell death
Cell Movement - drug effects
Cell survival
Cellular signal transduction
Crohn Disease - immunology
Crohn Disease - metabolism
Crohn Disease - pathology
Crohn's disease
Crohns disease
Cytokines
Defects
Disease susceptibility
E coli
Epithelial Cells - cytology
Escherichia coli
Escherichia coli - physiology
Experiments
Extracellular Signal-Regulated MAP Kinases - metabolism
Female
Formyl peptides
Gastroenterology
Gastrointestinal diseases
Granulocyte-Macrophage Colony-Stimulating Factor - metabolism
Granulocytes
Health aspects
Hepatology
Humans
Immune response
Immune system
Immunity
Inflammation
Inflammatory bowel disease
Inflammatory bowel diseases
Innate immunity
Interleukin 8
Interleukin-8 - pharmacology
Intestine
Kinases
Leukocyte migration
Leukocytes (neutrophilic)
Male
Middle Aged
N-Formylmethionine Leucyl-Phenylalanine - pharmacology
Neutrophils
Neutrophils - cytology
Neutrophils - drug effects
Neutrophils - immunology
Neutrophils - microbiology
Oxygen
Pathogenesis
Patients
Peripheral blood
Phosphorylation - drug effects
Proteolysis - drug effects
Proto-Oncogene Proteins c-akt - metabolism
Reactive oxygen species
Reactive Oxygen Species - metabolism
Remission
Signal transduction
Signal Transduction - drug effects
Signal Transduction - immunology
Signaling
Stat3 protein
STAT3 Transcription Factor - metabolism
Studies
Tumor necrosis factor-TNF
Young Adult
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Title Peripheral Neutrophil Functions and Cell Signalling in Crohn`s Disease
URI https://www.ncbi.nlm.nih.gov/pubmed/24367671
https://www.proquest.com/docview/1469701576
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https://doaj.org/article/8b07e07528a34ca5bc894ae13167c671
http://dx.doi.org/10.1371/journal.pone.0084521
Volume 8
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