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Griffonia simplicifolia I lectin mediates macrophage-induced cytotoxicity against Ehrlich ascites tumor

dc.contributor.authorMaddox, Daniel E.en_US
dc.contributor.authorGoldstein, Irwin J.en_US
dc.contributor.authorLoBuglio, Albert F.en_US
dc.date.accessioned2006-04-07T17:50:12Z
dc.date.available2006-04-07T17:50:12Z
dc.date.issued1982-07-15en_US
dc.identifier.citationMaddox, Daniel E., Goldstein, Irwin J., Lobuglio, Albert F. (1982/07/15)."Griffonia simplicifolia I lectin mediates macrophage-induced cytotoxicity against Ehrlich ascites tumor." Cellular Immunology 71(1): 202-207. <http://hdl.handle.net/2027.42/23924>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WCF-4DKVBF7-7W/2/fc11fd8eae9a68ad667a3cfba6c0c63aen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23924
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7139719&dopt=citationen_US
dc.description.abstractThe concurrent administration of Griffonia simplicifolia lectin into the peritoneal cavity of mice has been reported to protect them from challenge with Ehrlich ascites tumor cells. This study demonstrates that the GS I lectin is capable of binding to the surface of both inflammatory macrophages and Ehrlich ascites tumor cells and can mediate macrophage lectin-dependent cytotoxicity to this tumor cell line. The lectin was not found to be toxic to Ehrlich ascites tumor cells directly or to nonspecifically initiate complement-mediated lysis of these target cells. The macrophage lectin-dependent cytotoxicity could be specifically inhibited by the haptenic sugar methyl [alpha]--galactopyranoside. Thus, this lectin appears to be able to provide a linkage between effector macrophages and Ehrlich ascites tumor cells resulting in the triggering of a cytolytic event.en_US
dc.format.extent701111 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleGriffonia simplicifolia I lectin mediates macrophage-induced cytotoxicity against Ehrlich ascites tumoren_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, Section of Allergy and Clinical Immunology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumSection of Hematology/Oncology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.identifier.pmid7139719en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23924/1/0000169.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0008-8749(82)90509-3en_US
dc.identifier.sourceCellular Immunologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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