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  1. Article ; Online: Correspondence regarding "Effect of active smoking on the human bronchial epithelium transcriptome".

    Zuyderduyn, Scott D

    BMC genomics

    2009  Volume 10, Page(s) 82

    Abstract: ... used to show the consequences of these shortcomings.: Conclusion: Most of Chari et al.'s findings ...

    Abstract Background: In the work of Chari et al. entitled "Effect of active smoking on the human bronchial epithelium transcriptome" the authors use SAGE to identify candidate gene expression changes in bronchial brushings from never, former, and current smokers. These gene expression changes are categorized into those that are reversible or irreversible upon smoking cessation. A subset of these identified genes is validated on an independent cohort using RT-PCR. The authors conclude that their results support the notion of gene expression changes in the lungs of smokers which persist even after an individual has quit.
    Results: This correspondence raises questions about the validity of the approach used by the authors to analyze their data. The majority of the reported results suffer deficiencies due to the methods used. The most fundamental of these are explained in detail: biases introduced during data processing, lack of correction for multiple testing, and an incorrect use of clustering for gene discovery. A randomly generated "null" dataset is used to show the consequences of these shortcomings.
    Conclusion: Most of Chari et al.'s findings are consistent with what would be expected by chance alone. Although there is clear evidence of reversible changes in gene expression, the majority of those identified appear to be false positives. However, contrary to the authors' claims, no irreversible changes were identified. There is a broad consensus that genetic change due to smoking persists once an individual has quit smoking; unfortunately, this study lacks sufficient scientific rigour to support or refute this hypothesis or identify any specific candidate genes. The pitfalls of large-scale analysis, as exemplified here, may not be unique to Chari et al.
    MeSH term(s) Bronchi/metabolism ; Epithelium/metabolism ; False Positive Reactions ; Gene Expression ; Gene Expression Profiling ; Humans ; RNA, Messenger/genetics ; Smoking/genetics ; Smoking/metabolism ; Smoking Cessation
    Chemical Substances RNA, Messenger
    Language English
    Publishing date 2009-02-18
    Publishing country England
    Document type Comment ; Letter
    ISSN 1471-2164
    ISSN (online) 1471-2164
    DOI 10.1186/1471-2164-10-82
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Playing a dirty trick on airway smooth muscle: house dust mite does it again.

    Zuyderduyn, S / Hiemstra, P S

    The European respiratory journal

    2011  Volume 38, Issue 1, Page(s) 4–6

    MeSH term(s) Animals ; Asthma/metabolism ; Bronchi/metabolism ; CCAAT-Enhancer-Binding Protein-alpha/metabolism ; Gene Expression Regulation ; Humans ; Myocytes, Smooth Muscle/metabolism
    Chemical Substances CCAAT-Enhancer-Binding Protein-alpha
    Language English
    Publishing date 2011-07
    Publishing country England
    Document type Comment ; Editorial
    ZDB-ID 639359-7
    ISSN 1399-3003 ; 0903-1936
    ISSN (online) 1399-3003
    ISSN 0903-1936
    DOI 10.1183/09031936.00013111
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Correspondence regarding "Effect of active smoking on the human bronchial epithelium transcriptome"

    Zuyderduyn Scott D

    BMC Genomics, Vol 10, Iss 1, p

    2009  Volume 82

    Abstract: ... used to show the consequences of these shortcomings. Conclusion Most of Chari et al. 's findings are ...

    Abstract Abstract Background In the work of Chari et al. entitled "Effect of active smoking on the human bronchial epithelium transcriptome" the authors use SAGE to identify candidate gene expression changes in bronchial brushings from never, former, and current smokers. These gene expression changes are categorized into those that are reversible or irreversible upon smoking cessation. A subset of these identified genes is validated on an independent cohort using RT-PCR. The authors conclude that their results support the notion of gene expression changes in the lungs of smokers which persist even after an individual has quit. Results This correspondence raises questions about the validity of the approach used by the authors to analyze their data. The majority of the reported results suffer deficiencies due to the methods used. The most fundamental of these are explained in detail: biases introduced during data processing, lack of correction for multiple testing, and an incorrect use of clustering for gene discovery. A randomly generated "null" dataset is used to show the consequences of these shortcomings. Conclusion Most of Chari et al. 's findings are consistent with what would be expected by chance alone. Although there is clear evidence of reversible changes in gene expression, the majority of those identified appear to be false positives. However, contrary to the authors' claims, no irreversible changes were identified. There is a broad consensus that genetic change due to smoking persists once an individual has quit smoking; unfortunately, this study lacks sufficient scientific rigour to support or refute this hypothesis or identify any specific candidate genes. The pitfalls of large-scale analysis, as exemplified here, may not be unique to Chari et al .
    Keywords Genetics ; QH426-470 ; Biology (General) ; QH301-705.5 ; Science ; Q ; DOAJ:Genetics ; DOAJ:Biology ; DOAJ:Biology and Life Sciences
    Subject code 612
    Language English
    Publishing date 2009-02-01T00:00:00Z
    Publisher BioMed Central
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Whole transcriptome analysis reveals differential gene expression profile reflecting macrophage polarization in response to influenza A H5N1 virus infection.

    Zhang, Na / Bao, Yun-Juan / Tong, Amy Hin-Yan / Zuyderduyn, Scott / Bader, Gary D / Malik Peiris, J S / Lok, Si / Lee, Suki Man-Yan

    BMC medical genomics

    2018  Volume 11, Issue 1, Page(s) 20

    Abstract: Background: Avian influenza A H5N1 virus can cause lethal disease in humans. The virus can trigger severe pneumonia and lead to acute respiratory distress syndrome. Data from clinical, in vitro and in vivo suggest that virus-induced cytokine ... ...

    Abstract Background: Avian influenza A H5N1 virus can cause lethal disease in humans. The virus can trigger severe pneumonia and lead to acute respiratory distress syndrome. Data from clinical, in vitro and in vivo suggest that virus-induced cytokine dysregulation could be a contributory factor to the pathogenesis of human H5N1 disease. However, the precise mechanism of H5N1 infection eliciting the unique host response are still not well understood.
    Methods: To obtain a better understanding of the molecular events at the earliest time points, we used RNA-Seq to quantify and compare the host mRNA and miRNA transcriptomes induced by the highly pathogenic influenza A H5N1 (A/Vietnam/3212/04) or low virulent H1N1 (A/Hong Kong/54/98) viruses in human monocyte-derived macrophages at 1-, 3-, and 6-h post infection.
    Results: Our data reveals that two macrophage populations corresponding to M1 (classically activated) and M2 (alternatively activated) macrophage subtypes respond distinctly to H5N1 virus infection when compared to H1N1 virus or mock infection, a distinction that could not be made from previous microarray studies. When this confounding variable is considered in our statistical model, a clear set of dysregulated genes and pathways emerges specifically in H5N1 virus-infected macrophages at 6-h post infection, whilst was not found with H1N1 virus infection. Furthermore, altered expression of genes in these pathways, which have been previously implicated in viral host response, occurs specifically in the M1 subtype. We observe a significant up-regulation of genes in the RIG-I-like receptor signaling pathway. In particular, interferons, and interferon-stimulated genes are broadly affected. The negative regulators of interferon signaling, the suppressors of cytokine signaling, SOCS-1 and SOCS-3, were found to be markedly up-regulated in the initial round of H5N1 virus replication. Elevated levels of these suppressors could lead to the eventual suppression of cellular antiviral genes, contributing to pathophysiology of H5N1 virus infection.
    Conclusions: Our study provides important mechanistic insights into the understanding of H5N1 viral pathogenesis and the multi-faceted host immune responses. The dysregulated genes could be potential candidates as therapeutic targets for treating H5N1 disease.
    MeSH term(s) Gene Expression Profiling ; Humans ; Immunity, Innate/genetics ; Influenza A Virus, H1N1 Subtype/physiology ; Influenza A Virus, H5N1 Subtype/physiology ; Macrophages/cytology ; Macrophages/immunology ; Macrophages/metabolism ; Macrophages/virology ; MicroRNAs/genetics
    Chemical Substances MicroRNAs
    Language English
    Publishing date 2018-02-23
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 1755-8794
    ISSN (online) 1755-8794
    DOI 10.1186/s12920-018-0335-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Interleukin 13 exposure enhances vitamin D-mediated expression of the human cathelicidin antimicrobial peptide 18/LL-37 in bronchial epithelial cells.

    Schrumpf, J A / van Sterkenburg, M A J A / Verhoosel, R M / Zuyderduyn, S / Hiemstra, P S

    Infection and immunity

    2012  Volume 80, Issue 12, Page(s) 4485–4494

    Abstract: Vitamin D is an important regulator of the expression of antimicrobial peptides, and vitamin D deficiency is associated with respiratory infections. Regulating expression of antimicrobial peptides, such as the human cathelicidin antimicrobial peptide 18 ( ...

    Abstract Vitamin D is an important regulator of the expression of antimicrobial peptides, and vitamin D deficiency is associated with respiratory infections. Regulating expression of antimicrobial peptides, such as the human cathelicidin antimicrobial peptide 18 (hCAP18)/LL-37, by vitamin D in bronchial epithelial cells requires local conversion of 25(OH)-vitamin D(3) (25D(3)) into its bioactive metabolite, 1,25(OH)(2)-vitamin D(3) (1,25D(3)), by CYP27B1. Low circulating vitamin D levels in childhood asthma are associated with more-severe exacerbations, which are often associated with infections. Atopic asthma is accompanied by Th2-driven inflammation mediated by cytokines such as interleukin 4 (IL-4) and IL-13, and the effect of these cytokines on vitamin D metabolism and hCAP18/LL-37 expression is unknown. Therefore, we investigated this with well-differentiated bronchial epithelial cells. To this end, cells were treated with IL-13 with and without 25D(3), and expression of hCAP18/LL-37, CYP27B1, the 1,25D(3)-inactivating enzyme CYP24A1, and vitamin D receptor was assessed by quantitative PCR. We show that IL-13 enhances the ability of 25D(3) to increase expression of hCAP18/LL-37 and CYP24A1. In addition, exposure to IL-13 resulted in increased CYP27B1 expression, whereas vitamin D receptor (VDR) expression was not significantly affected. The enhancing effect of IL-13 on 25D(3)-mediated expression of hCAP18/LL-37 was further confirmed using SDS-PAGE Western blotting and immunofluorescence staining. In conclusion, we demonstrate that IL-13 induces vitamin D-dependent hCAP18/LL-37 expression, most likely by increasing CYP27B1. These data suggest that Th2 cytokines regulate the vitamin D metabolic pathway in bronchial epithelial cells.
    MeSH term(s) Adjuvants, Immunologic/genetics ; Adjuvants, Immunologic/metabolism ; Antimicrobial Cationic Peptides ; Bronchi/cytology ; Bronchi/drug effects ; Bronchi/metabolism ; Cathelicidins/genetics ; Cathelicidins/metabolism ; Cells, Cultured ; Cholecalciferol/genetics ; Cholecalciferol/metabolism ; Cholecalciferol/pharmacology ; Epithelial Cells/drug effects ; Epithelial Cells/metabolism ; Humans ; Interleukin-13/genetics ; Interleukin-13/metabolism ; Interleukin-13/pharmacology ; Receptors, Calcitriol/genetics ; Receptors, Calcitriol/metabolism ; Up-Regulation/drug effects ; Vitamin D/analogs & derivatives ; Vitamin D/genetics ; Vitamin D/metabolism
    Chemical Substances Adjuvants, Immunologic ; Antimicrobial Cationic Peptides ; Cathelicidins ; Interleukin-13 ; Receptors, Calcitriol ; Vitamin D (1406-16-2) ; Cholecalciferol (1C6V77QF41) ; ropocamptide (3DD771JO2H)
    Language English
    Publishing date 2012-10-08
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 218698-6
    ISSN 1098-5522 ; 0019-9567
    ISSN (online) 1098-5522
    ISSN 0019-9567
    DOI 10.1128/IAI.06224-11
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: TGF-beta differentially regulates TH2 cytokine-induced eotaxin and eotaxin-3 release by human airway smooth muscle cells.

    Zuyderduyn, Suzanne / Hiemstra, Pieter S / Rabe, Klaus F

    The Journal of allergy and clinical immunology

    2004  Volume 114, Issue 4, Page(s) 791–798

    Abstract: Background: Human airway smooth muscle cells (HASMs) are involved in the pathogenesis of asthma. By producing chemokines, HASMs play a role in the inflammatory processes observed in this disease. Eotaxin, eotaxin-2, and eotaxin-3 are important ... ...

    Abstract Background: Human airway smooth muscle cells (HASMs) are involved in the pathogenesis of asthma. By producing chemokines, HASMs play a role in the inflammatory processes observed in this disease. Eotaxin, eotaxin-2, and eotaxin-3 are important chemoattractants for eosinophils, and these chemokines are expressed during different phases of the allergic reaction. TH2 cytokines and TGF-beta can be found in increased levels in patients with asthma, and these cytokines may be involved in the regulation of chemokine expression.
    Objective: The aim of this study was to determine the effect of TH2 cytokines and TGF-beta on the regulation of expression of eotaxin, eotaxin-2, and eotaxin-3 by HASMs.
    Methods: HASMs were incubated for 24 hours with IL-4, IL-13, TGF-beta1, or combinations of these cytokines. Protein and mRNA levels of eotaxin and eotaxin-3 were evaluated by sandwich ELISA and reverse transcriptase-PCR.
    Results: IL-4 and IL-13 induced mRNA and protein for both eotaxin and eotaxin-3. Eotaxin-2 mRNA and protein were not detected in HASMs. TGF-beta alone did not induce expression of the eotaxins. However, in combination with IL-4 or IL-13, TGF-beta enhanced eotaxin production and inhibited TH2 cytokine-induced eotaxin-3 production.
    Conclusion: TGF-beta differentially regulates TH2 cytokine-induced eotaxin and eotaxin-3 release.
    MeSH term(s) Bronchi/immunology ; Chemokine CCL11 ; Chemokine CCL26 ; Chemokines, CC/immunology ; Humans ; Interleukin-13/immunology ; Interleukin-4/immunology ; Myocytes, Smooth Muscle/immunology ; Pneumonia/immunology ; Th2 Cells/immunology ; Transforming Growth Factor beta/immunology
    Chemical Substances CCL11 protein, human ; CCL26 protein, human ; Chemokine CCL11 ; Chemokine CCL26 ; Chemokines, CC ; Interleukin-13 ; Transforming Growth Factor beta ; Interleukin-4 (207137-56-2)
    Language English
    Publishing date 2004-10
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 121011-7
    ISSN 1085-8725 ; 1097-6825 ; 0091-6749
    ISSN (online) 1085-8725 ; 1097-6825
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2004.06.037
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The antimicrobial peptide LL-37 enhances IL-8 release by human airway smooth muscle cells.

    Zuyderduyn, Suzanne / Ninaber, Dennis K / Hiemstra, Pieter S / Rabe, Klaus F

    The Journal of allergy and clinical immunology

    2006  Volume 117, Issue 6, Page(s) 1328–1335

    Abstract: Background: Human airway smooth muscle (HASM) cells release various chemokines that are involved in recruitment of inflammatory cells, which can be found within or in the vicinity of the airway smooth muscle layer in patients with inflammatory lung ... ...

    Abstract Background: Human airway smooth muscle (HASM) cells release various chemokines that are involved in recruitment of inflammatory cells, which can be found within or in the vicinity of the airway smooth muscle layer in patients with inflammatory lung diseases. Inflammatory cells contain antimicrobial peptides including the cathelicidin LL-37 and neutrophil defensins (HNP1-3).
    Objective: The aim of the study was to determine the effects of antimicrobial peptides on IL-8 (CXC chemokine ligand 8) release by HASM cells, and to study the underlying mechanisms.
    Methods: Human airway smooth muscle cells were stimulated with LL-37 and HNP1-3, and IL-8 protein and mRNA levels were determined by sandwich ELISA and PCR. Phosphorylation of extracellular signal-regulated kinase (ERK) 1/2 was detected by using Western blot.
    Results: LL-37 enhanced IL-8 release by HASM cells, which was dependent on ERK1/2 activation. Receptors known to be involved in LL-37-induced signaling, including the epidermal growth factor receptor and formyl peptide receptors, were not involved in LL-37 signaling in HASM cells. The purinergic receptor antagonist suramin did block LL-37-induced ERK1/2 phosphorylation and IL-8 release, and expression of mRNA for the purinergic receptor P2X(7) was detected in HASM cells. HNP1-3 did increase ERK1/2 phosphorylation, but did not enhance IL-8 release by HASM cells.
    Conclusion: These data show that HASM cells respond to the antimicrobial peptide LL-37 by releasing IL-8, suggesting that LL-37 is a regulator of the inflammatory process in various inflammatory lung diseases by enhancing IL-8 production.
    Clinical implications: LL-37 released by inflammatory cells may amplify inflammation through induction of IL-8 release by airway smooth muscle.
    MeSH term(s) Antimicrobial Cationic Peptides/genetics ; Antimicrobial Cationic Peptides/physiology ; Cells, Cultured ; Humans ; Inflammation/enzymology ; Inflammation/immunology ; Inflammation/metabolism ; Interleukin-8/metabolism ; Lung/enzymology ; Lung/immunology ; Lung/metabolism ; Lung/pathology ; Myocytes, Smooth Muscle/immunology ; Myocytes, Smooth Muscle/metabolism ; Up-Regulation/immunology ; alpha-Defensins/physiology
    Chemical Substances Antimicrobial Cationic Peptides ; Interleukin-8 ; alpha-Defensins ; human neutrophil peptide 1 ; human neutrophil peptide 2 ; human neutrophil peptide 3 ; ropocamptide (3DD771JO2H)
    Language English
    Publishing date 2006-06-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 121011-7
    ISSN 1085-8725 ; 1097-6825 ; 0091-6749
    ISSN (online) 1085-8725 ; 1097-6825
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2006.03.022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Treating asthma means treating airway smooth muscle cells.

    Zuyderduyn, S / Sukkar, M B / Fust, A / Dhaliwal, S / Burgess, J K

    The European respiratory journal

    2008  Volume 32, Issue 2, Page(s) 265–274

    Abstract: Asthma is characterised by airway hyperresponsiveness, airway inflammation and airway remodelling. Airway smooth muscle cells are known to be the main effector cells of airway narrowing. In the present paper, studies will be discussed that have led to a ... ...

    Abstract Asthma is characterised by airway hyperresponsiveness, airway inflammation and airway remodelling. Airway smooth muscle cells are known to be the main effector cells of airway narrowing. In the present paper, studies will be discussed that have led to a novel view of the role of airway smooth muscle in the pathogenesis of asthma in which airway hyperresponsiveness, remodelling and inflammation are, at least in part, attributable to airway smooth muscle. Furthermore, how this new view may lead to a change in the phenotyping and treatment of patients with asthma will be discussed.
    MeSH term(s) Adolescent ; Adult ; Animals ; Asthma/diagnosis ; Asthma/therapy ; Cell Membrane/metabolism ; Humans ; Hypertrophy ; Inflammation ; Models, Biological ; Myocytes, Smooth Muscle/metabolism ; Nematode Infections/metabolism ; Phenotype ; Pulmonary Alveoli/pathology ; Respiratory System/pathology
    Language English
    Publishing date 2008-08
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 639359-7
    ISSN 1399-3003 ; 0903-1936
    ISSN (online) 1399-3003
    ISSN 0903-1936
    DOI 10.1183/09031936.00051407
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Whole transcriptome analysis reveals differential gene expression profile reflecting macrophage polarization in response to influenza A H5N1 virus infection

    Na Zhang / Yun-Juan Bao / Amy Hin-Yan Tong / Scott Zuyderduyn / Gary D. Bader / J. S. Malik Peiris / Si Lok / Suki Man-Yan Lee

    BMC Medical Genomics, Vol 11, Iss 1, Pp 1-

    2018  Volume 14

    Abstract: Abstract Background Avian influenza A H5N1 virus can cause lethal disease in humans. The virus can trigger severe pneumonia and lead to acute respiratory distress syndrome. Data from clinical, in vitro and in vivo suggest that virus-induced cytokine ... ...

    Abstract Abstract Background Avian influenza A H5N1 virus can cause lethal disease in humans. The virus can trigger severe pneumonia and lead to acute respiratory distress syndrome. Data from clinical, in vitro and in vivo suggest that virus-induced cytokine dysregulation could be a contributory factor to the pathogenesis of human H5N1 disease. However, the precise mechanism of H5N1 infection eliciting the unique host response are still not well understood. Methods To obtain a better understanding of the molecular events at the earliest time points, we used RNA-Seq to quantify and compare the host mRNA and miRNA transcriptomes induced by the highly pathogenic influenza A H5N1 (A/Vietnam/3212/04) or low virulent H1N1 (A/Hong Kong/54/98) viruses in human monocyte-derived macrophages at 1-, 3-, and 6-h post infection. Results Our data reveals that two macrophage populations corresponding to M1 (classically activated) and M2 (alternatively activated) macrophage subtypes respond distinctly to H5N1 virus infection when compared to H1N1 virus or mock infection, a distinction that could not be made from previous microarray studies. When this confounding variable is considered in our statistical model, a clear set of dysregulated genes and pathways emerges specifically in H5N1 virus-infected macrophages at 6-h post infection, whilst was not found with H1N1 virus infection. Furthermore, altered expression of genes in these pathways, which have been previously implicated in viral host response, occurs specifically in the M1 subtype. We observe a significant up-regulation of genes in the RIG-I-like receptor signaling pathway. In particular, interferons, and interferon-stimulated genes are broadly affected. The negative regulators of interferon signaling, the suppressors of cytokine signaling, SOCS-1 and SOCS-3, were found to be markedly up-regulated in the initial round of H5N1 virus replication. Elevated levels of these suppressors could lead to the eventual suppression of cellular antiviral genes, contributing to pathophysiology ...
    Keywords Influenza A virus ; H5N1 ; Macrophage polarization ; Transcriptomics ; RNA-Seq ; Internal medicine ; RC31-1245 ; Genetics ; QH426-470
    Subject code 570
    Language English
    Publishing date 2018-02-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Pro-inflammatory mechanisms of muscarinic receptor stimulation in airway smooth muscle.

    Oenema, Tjitske A / Kolahian, Saeed / Nanninga, Janke E / Rieks, Daniëlle / Hiemstra, Pieter S / Zuyderduyn, Suzanne / Halayko, Andrew J / Meurs, Herman / Gosens, Reinoud

    Respiratory research

    2010  Volume 11, Page(s) 130

    Abstract: ... by acting on muscarinic receptors, is also involved in airway inflammation and remodelling. The mechanism(s ...

    Abstract Background: Acetylcholine, the primary parasympathetic neurotransmitter in the airways, plays an important role in bronchoconstriction and mucus production. Recently, it has been shown that acetylcholine, by acting on muscarinic receptors, is also involved in airway inflammation and remodelling. The mechanism(s) by which muscarinic receptors regulate inflammatory responses are, however, still unknown.
    Methods: The present study was aimed at characterizing the effect of muscarinic receptor stimulation on cytokine secretion by human airway smooth muscle cells (hASMc) and to dissect the intracellular signalling mechanisms involved. hASMc expressing functional muscarinic M2 and M3 receptors were stimulated with the muscarinic receptor agonist methacholine, alone, and in combination with cigarette smoke extract (CSE), TNF-α, PDGF-AB or IL-1β.
    Results: Muscarinic receptor stimulation induced modest IL-8 secretion by itself, yet augmented IL-8 secretion in combination with CSE, TNF-α or PDGF-AB, but not with IL-1β. Pretreatment with GF109203X, a protein kinase C (PKC) inhibitor, completely normalized the effect of methacholine on CSE-induced IL-8 secretion, whereas PMA, a PKC activator, mimicked the effects of methacholine, inducing IL-8 secretion and augmenting the effects of CSE. Similar inhibition was observed using inhibitors of IκB-kinase-2 (SC514) and MEK1/2 (U0126), both downstream effectors of PKC. Accordingly, western blot analysis revealed that methacholine augmented the degradation of IκBα and the phosphorylation of ERK1/2 in combination with CSE, but not with IL-1β in hASMc.
    Conclusions: We conclude that muscarinic receptors facilitate CSE-induced IL-8 secretion by hASMc via PKC dependent activation of IκBα and ERK1/2. This mechanism could be of importance for COPD patients using anticholinergics.
    MeSH term(s) Acetylcholine/pharmacology ; Bronchi/metabolism ; Cells, Cultured ; Humans ; Inflammation Mediators/metabolism ; Inflammation Mediators/physiology ; Interleukin-6/metabolism ; Interleukin-8/metabolism ; Muscle, Smooth/metabolism ; Myocytes, Smooth Muscle/metabolism ; Receptor, Muscarinic M2/metabolism ; Receptor, Muscarinic M2/physiology ; Receptor, Muscarinic M3/metabolism ; Receptor, Muscarinic M3/physiology ; Receptors, Muscarinic/metabolism ; Receptors, Muscarinic/physiology ; Signal Transduction/immunology ; Smoking/metabolism
    Chemical Substances Inflammation Mediators ; Interleukin-6 ; Interleukin-8 ; Receptor, Muscarinic M2 ; Receptor, Muscarinic M3 ; Receptors, Muscarinic ; Acetylcholine (N9YNS0M02X)
    Language English
    Publishing date 2010-09-28
    Publishing country England
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2041675-1
    ISSN 1465-993X ; 1465-993X
    ISSN (online) 1465-993X
    ISSN 1465-993X
    DOI 10.1186/1465-9921-11-130
    Database MEDical Literature Analysis and Retrieval System OnLINE

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