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Impaired Hepatocyte Regeneration in Toll-Like Receptor 4 Mutant Mice

dc.contributor.authorSu, Grace L.en_US
dc.contributor.authorWang, Stewart C.en_US
dc.contributor.authorAminlari, Alirezaen_US
dc.contributor.authorTipoe, George L.en_US
dc.contributor.authorSteinstraesser, Larsen_US
dc.contributor.authorNanji, Amin A.en_US
dc.date.accessioned2006-09-11T14:47:31Z
dc.date.available2006-09-11T14:47:31Z
dc.date.issued2004-05en_US
dc.identifier.citationSu, Grace L.; Wang, Stewart C.; Aminlari, Alireza; Tipoe, George L.; Steinstraesser, Lars; Nanji, Amin; (2004). "Impaired Hepatocyte Regeneration in Toll-Like Receptor 4 Mutant Mice." Digestive Diseases and Sciences 49(5): 843-849. <http://hdl.handle.net/2027.42/44432>en_US
dc.identifier.issn0163-2116en_US
dc.identifier.issn1573-2568en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44432
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15259507&dopt=citationen_US
dc.description.abstractMultiple lines of evidence suggest a role for endogenous lipopolysaccharides in toxin-induced liver injury. Toll-like receptor 4 has recently been implicated as a cell surface receptor important for lipopolysaccharide responsiveness. In these experiments, we sought to determine the role of toll-like receptor 4 in acute liver injury by carbon tetrachloride by utilizing the naturally occurring toll-like receptor 4 mutant and wild-type mice strains. Mice were injected with either carbon tetrachloride or the carrier. Serum transaminase levels peaked at 24 hr after carbon tetrachloride administration for both wild-type and mutant mice, with no significant histological difference in initial liver injury between the two groups. However, an overall decrease in hepatocyte proliferation was found in the mutant mice. Examination of the liver tissue revealed significant decreases in intrahepatic expressions of proinflammatory mediators. In conclusion, our results suggest that toll-like receptor 4 is important in the hepatic regenerative response to CCl 4 liver injury via its role in modulating the inflammatory response to hepatic injury.en_US
dc.format.extent1045433 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherHepatotoxicityen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherGastroenterologyen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherHepatologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherTransplant Surgeryen_US
dc.subject.otherLiveren_US
dc.subject.otherEndotoxinsen_US
dc.subject.otherCytokinesen_US
dc.titleImpaired Hepatocyte Regeneration in Toll-Like Receptor 4 Mutant Miceen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan School of Medicine, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan School of Medicine, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumMedical Service, Veterans Affairs Ann Arbor Health Care Systems, and Department of Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan School of Medicine, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Anatomy, University of Hong Kong, Hong Kongen_US
dc.contributor.affiliationotherDepartment of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid15259507en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44432/1/10620_2004_Article_490703.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/B:DDAS.0000030097.52476.aaen_US
dc.identifier.sourceDigestive Diseases and Sciencesen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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