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dc.contributor.supervisorGOUNNI, Abdelilah SOUSSI (Immunology)en
dc.contributor.authorDRAGON, Stephane
dc.date.accessioned2010-04-09T13:51:07Z
dc.date.available2010-04-09T13:51:07Z
dc.date.issued2010-04-09T13:51:07Z
dc.identifier.citationDragon S, Saffar AS, Shan L, Gounni AS. (2008) Mol Immunol. Jan;45(1):160-8en
dc.identifier.citationDragon S, Rahman MS, Yang J, Unruh H, Halayko AJ, Gounni AS. (2007) Am J Physiol Lung Cell Mol Physiol. Apr;292(4):L1023-9en
dc.identifier.urihttp://hdl.handle.net/1993/3945
dc.description.abstractImmunopathological disorders are no longer defined by dysregulated T-helper (Th) type 1/ Th2 responses but account for modulatory cell types such as regulatory and Th17 cells. The newly defined Th17 subset is an effector memory subtype which regulates mucosal host defense responses. A distinctive feature of interleukin (IL)-17 is its ability to invoke neutrophilic responses and to synergize cytokine responses in proximal structural cells. This effect is most evident for proinflammatory cytokines and neutrophil-mobilizing chemokines which are under the regulatory control of the canonical, nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway. The uniqueness of the IL-17A receptor (IL-17RA) signal transduction pathway however has been a limiting factor in uncovering IL-17-mediated effector functions since the receptor bears little homology to other known receptors and contains a unique cytoplasmic consensus binding motif. Hence, the composition, dynamics and subunit interactions of the IL-17R complex have become an emerging area of research where novel recruitment motifs and adaptor proteins are actively being explored. Our study sought to uncover the signal transduction and molecular mechanisms mediating the initiation and amplification responses induced by IL-17. We hypothesize that (i) IL-17 represents a key cytokine which initiates inflammatory responses by acting on proximal structural cells to rapidly release neutrophil-mobilizing chemokines and myeloid growth factors and that (ii) IL-17 directly promotes survival responses of immune effector cells. Genomic analysis of stimulated human airway smooth muscle cells support the proinflammatory nature of IL-17 as NF-κB associated genes and chemokines were most significantly upregulated within 2 hours. However, IL-17 induced a modest fold increase in gene expression levels whereby only 4 genes achieved greater than 2 fold increases. This, along with the observation that IL-17 enhanced IL-1β-mediated CXCL8 expression via transcriptional promoter activation levels and post-transcriptional mRNA stabilization mechanisms suggests that IL-17 cooperatively functions with secondary cytokines to mediate inflammatory responses. Despite activating the p38-mitogen-activated protein kinase (MAPK) signaling pathway in peripheral blood neutrophils, IL-17 did not directly affect the apoptotic capacity of these cells but unexpectedly antagonized the survival response mediated by the granulocyte-macrophage colony stimulating factor (GM-CSF). Collectively, our results suggest that IL-17 is a potent synergistic cytokine which signals via the MAPK-NF-κB pathway to indirectly recruit neutrophils via CXC-chemokines produced by non-hematopoietic cells and that IL-17 may potentially dampen inflammatory responses by directly antagonizing inflammatory effector cells.en
dc.format.extent4693022 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectHumanen
dc.subjectInflammationen
dc.subjectCytokinesen
dc.subjectIL-17en
dc.subjectIL-1betaen
dc.subjectIL-22en
dc.subjectCXCL-8en
dc.subjectairway smooth muscle cellsen
dc.subjectneutrophilsen
dc.subjectIL-17Ren
dc.subjectsignal transductionen
dc.subjectgene expressionen
dc.subjectapoptosisen
dc.titleMolecular Signaling Mechanisms and Effector Functions of the Interleukin-17 Receptor in Human Airway Smooth Muscle Cells and Polymorphonuclear Neutrophilsen
dc.typeinfo:eu-repo/semantics/doctoralThesis
dc.typedoctoral thesisen_US
dc.degree.disciplineImmunologyen_US
dc.contributor.examiningcommitteeMARSHALL, Aaron (Immunology) GIBSON, Spencer (Biochemistry and Medical Genetics) HALAYKO, Andrew (Physiology) KUMAR, Ashok (Pathology and Laboratory Medicine University of Ottawa)en
dc.degree.levelDoctor of Philosophy (Ph.D.)en_US
dc.description.noteMay 2010en


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