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dc.contributor.authorLatz, Eicke
dc.contributor.authorVisintin, Alberto
dc.contributor.authorLien, Egil
dc.contributor.authorFitzgerald, Katherine A.
dc.contributor.authorEspevik, Terje
dc.contributor.authorGolenbock, Douglas T.
dc.date2022-08-11T08:09:08.000
dc.date.accessioned2022-08-23T16:18:40Z
dc.date.available2022-08-23T16:18:40Z
dc.date.issued2003-12-22
dc.date.submitted2011-03-25
dc.identifier.citationJ Endotoxin Res. 2003;9(6):375-80. <a href="http://dx.doi.org/10.1177/09680519030090061101">Link to article on publisher's site</a>
dc.identifier.issn0968-0519 (Linking)
dc.identifier.doi10.1177/09680519030090061101
dc.identifier.pmid14733724
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34871
dc.description.abstractBacterial lipopolysaccharides (LPSs) are recognized in mammals by a receptor complex composed of CD14, Toll-like receptor 4 (TLR4), and MD-2. The mechanism of TLR4 function remains to be elucidated. We constructed chimeric TLR molecules C-terminally fused to fluorescent proteins and stably expressed these chimeric constructs in cells. Confocal microscopy revealed TLR4 to be expressed on the plasma membrane and the Golgi apparatus. Time-lapse confocal imaging showed rapid recycling of TLR4/CD14/MD-2 complexes between the Golgi and the plasma membrane. Membrane TLR4 engagement by antibody was sufficient to induce signaling and pharmacological disruption of the Golgi did not affect cellular responses to LPS. Thus, LPS signaling commences after LPS recognition by surface-expressed TLR4 independent of LPS trafficking to the Golgi.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=14733724&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1177/09680519030090061101
dc.subjectAntigens, CD14
dc.subjectCell Line
dc.subjectCell Membrane
dc.subjectCulture Media
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectGolgi Apparatus
dc.subjectGreen Fluorescent Proteins
dc.subjectHumans
dc.subject*Inflammation
dc.subjectInterleukin-8
dc.subjectKidney
dc.subjectLipopolysaccharides
dc.subjectLuminescent Proteins
dc.subjectMicroscopy, Confocal
dc.subjectRecombinant Fusion Proteins
dc.subject*Signal Transduction
dc.subjectImmunology and Infectious Disease
dc.titleThe LPS receptor generates inflammatory signals from the cell surface
dc.typeJournal Article
dc.source.journaltitleJournal of endotoxin research
dc.source.volume9
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/infdis_pp/100
dc.identifier.contextkey1901424
html.description.abstract<p>Bacterial lipopolysaccharides (LPSs) are recognized in mammals by a receptor complex composed of CD14, Toll-like receptor 4 (TLR4), and MD-2. The mechanism of TLR4 function remains to be elucidated. We constructed chimeric TLR molecules C-terminally fused to fluorescent proteins and stably expressed these chimeric constructs in cells. Confocal microscopy revealed TLR4 to be expressed on the plasma membrane and the Golgi apparatus. Time-lapse confocal imaging showed rapid recycling of TLR4/CD14/MD-2 complexes between the Golgi and the plasma membrane. Membrane TLR4 engagement by antibody was sufficient to induce signaling and pharmacological disruption of the Golgi did not affect cellular responses to LPS. Thus, LPS signaling commences after LPS recognition by surface-expressed TLR4 independent of LPS trafficking to the Golgi.</p>
dc.identifier.submissionpathinfdis_pp/100
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages375-80


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