Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.ppat.0030060
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dc.titleA novel TLR4-mediated signaling pathway leading to IL-6 responses in human bladder epithelial cells
dc.contributor.authorSong J.
dc.contributor.authorDuncan M.J.
dc.contributor.authorLi G.
dc.contributor.authorChan C.
dc.contributor.authorGrady R.
dc.contributor.authorStapleton A.
dc.contributor.authorAbraham S.N.
dc.date.accessioned2019-11-08T00:59:14Z
dc.date.available2019-11-08T00:59:14Z
dc.date.issued2007
dc.identifier.citationSong J., Duncan M.J., Li G., Chan C., Grady R., Stapleton A., Abraham S.N. (2007). A novel TLR4-mediated signaling pathway leading to IL-6 responses in human bladder epithelial cells. PLoS Pathogens 3 (4) : 541-552. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.ppat.0030060
dc.identifier.issn15537366
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161867
dc.description.abstractThe vigorous cytokine response of immune cells to Gram-negative bacteria is primarily mediated by a recognition molecule, Toll-like receptor 4 (TLR4), which recognizes lipopolysaccharide (LPS) and initiates a series of intracellular NF-?B-associated signaling events. Recently, bladder epithelial cells (BECs) were reported to express TLR4 and to evoke a vigorous cytokine response upon exposure to LPS. We examined intracellular signaling events in human BECs leading to the production of IL-6, a major urinary cytokine, following activation by Escherichia coli and isolated LPS. We observed that in addition to the classical NF-?B-associated pathway, TLR4 triggers a distinct and more rapid signaling response involving, sequentially, Ca 2+, adenylyl cyclase 3-generated cAMP, and a transcriptional factor, cAMP response element-binding protein. This capacity of BECs to mobilize secondary messengers and evoke a more rapid IL-6 response might be critical in their role as first responders to microbial challenge in the urinary tract. � 2007 Song et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectadenylate cyclase
dc.subjectcyclic AMP
dc.subjectcyclic AMP responsive element binding protein binding protein
dc.subjectcytokine
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectinterleukin 6
dc.subjectlipopolysaccharide
dc.subjecttoll like receptor 4
dc.subjecttranscription factor
dc.subjectadenylate cyclase
dc.subjectbacterial RNA
dc.subjectcalcium
dc.subjectCREBBP protein, human
dc.subjectcyclic AMP
dc.subjectcyclic AMP responsive element binding protein binding protein
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectlipopolysaccharide
dc.subjectTLR4 protein, human
dc.subjectunclassified drug
dc.subjectarticle
dc.subjectbladder epithelium
dc.subjectcalcium cell level
dc.subjectcell motility
dc.subjectcontrolled study
dc.subjectepithelium cell
dc.subjectEscherichia coli
dc.subjecthuman
dc.subjecthuman cell
dc.subjectnonhuman
dc.subjectprotein analysis
dc.subjectprotein expression
dc.subjectprotein phosphorylation
dc.subjectprotein secretion
dc.subjectsignal transduction
dc.subjectbladder
dc.subjectcytology
dc.subjectEnterobacter infection
dc.subjectEscherichia coli
dc.subjectfimbria
dc.subjectgenetics
dc.subjectimmunology
dc.subjectmetabolism
dc.subjectmicrobiology
dc.subjectphosphorylation
dc.subjectsignal transduction
dc.subjectEscherichia coli
dc.subjectNegibacteria
dc.subjectAdenylate Cyclase
dc.subjectCalcium
dc.subjectCREB-Binding Protein
dc.subjectCyclic AMP
dc.subjectEpithelial Cells
dc.subjectEscherichia coli
dc.subjectEscherichia coli Infections
dc.subjectFimbriae, Bacterial
dc.subjectHumans
dc.subjectInterleukin-6
dc.subjectLipopolysaccharides
dc.subjectNF-kappa B
dc.subjectPhosphorylation
dc.subjectRNA, Bacterial
dc.subjectSignal Transduction
dc.subjectToll-Like Receptor 4
dc.subjectUrinary Bladder
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1371/journal.ppat.0030060
dc.description.sourcetitlePLoS Pathogens
dc.description.volume3
dc.description.issue4
dc.description.page541-552
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