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dc.contributor.authorCao, Qi
dc.date.accessioned2013-05-01T12:54:39Z
dc.date.available2013-05-01T12:54:39Z
dc.date.issued2013-05-01
dc.identifier.urihttp://hdl.handle.net/10222/21905
dc.description.abstractHuman colonic epithelial cell lines (T84, Caco2 and HT-29) were used to address the question of whether intestinal epithelial cells can detect and respond to activated complement via the anaphylatoxin receptors, considering the gut is host to large numbers of bacteria. All cell lines possess C3aR, C5aR and C5L2. Confocal microscopy confirmed that cells express apical C5aR and C5L2. C3a and C5a up-regulated CXCL8 and CXCL10 mRNA but not secreted protein levels within 48 hours. Protein levels were not increased using simultaneous treatment with subthreshold concentrations of LPS or TNF plus anaphylatoxin. C3a and C5a also increased the permeability of polarized monolayers. Anaphylatoxins also promoted the proliferation of T84 and HT-29. Inhibition of ERK signaling abolished these effects of anaphylatoxins. Our findings that multiple human cell lines possess functional anaphylatoxin receptors indicates that the colonic epithelium likely responds to the activation of complement in the lumen with an inflammatory outcome.en_US
dc.language.isoenen_US
dc.subjectAnaphylatoxinen_US
dc.subjectAnaphylatoxin receptoren_US
dc.subjectChemokineen_US
dc.subjectHuman colonic epithelial cellen_US
dc.titleExpression and Role of Anaphylatoxin Receptors on Human Colonic Epithelial Cellsen_US
dc.date.defence2012-02-20
dc.contributor.departmentDepartment of Microbiology & Immunologyen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.external-examinerDr. Thomas Issekutzen_US
dc.contributor.graduate-coordinatorDr. Brent Johnsonen_US
dc.contributor.thesis-readerDr. David Hoskinen_US
dc.contributor.thesis-readerDr. Elizabeth Cowleyen_US
dc.contributor.thesis-supervisorDr. Andrew Stadnyken_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseNot Applicableen_US
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