Show simple item record

dc.creatorWang, Mingjun
dc.creatorHarhaji Trajković, Ljubica
dc.creatorLamberth, K
dc.creatorHarndahl, M
dc.creatorBuus, S
dc.creatorHeegaard, NHH
dc.creatorClaesson, MH
dc.creatorNissen, Mogens H
dc.date.accessioned2017-11-23T11:12:37Z
dc.date.available2015-11-17T10:26:51Z
dc.date.issued2009sr
dc.identifier.issn0300-9475sr
dc.identifier.otherRad_konverzija_3458sr
dc.identifier.urihttps://ibiss-r.rcub.bg.ac.rs/handle/123456789/1463
dc.description.abstractBeta2-microglobulin (beta 2m) is the light chain of major histocompatibility complex class I (MHC-I) molecules, and is a prerequisite for the binding of peptides to the heavy chain and their presentation to CD8(+) T cells. beta 2m can be modified in vivo and in vitro by proteolytic cleavage by complement C1 and subsequent carboxypeptidase B-like activity - processes that lead to the generation of desLys(58)beta 2m (d beta 2m). This work aims to study the effect of d beta 2m on peptide binding to MHC-I, the influence of d beta 2m on the binding of beta 2m to the MHC-I heavy chain and the biological activity of d beta 2m. Both beta 2m and d beta 2m are able to support the generation of MHC-I/peptide complexes at 18 degrees C, but complexes formed in the presence of d beta 2m destabilize at 37 degrees C. Moreover, a 250 times higher concentration of d beta 2m than of beta 2m is needed to displace MHC-I associated beta 2m from the cell surface. In addition, only beta 2m is able to restore MHC-I/peptide complex formation on acid-treated cells whereas d beta 2m appears to bind preferentially to denatured MHC-I heavy chains. In cell cultures, exogenously added d beta 2m, but not beta 2m, induces apoptotic cell death in monocytic leukaemic cell lines but spares other kinds of leukaemic cells. Additionally, the presence of d beta 2m, and to a lesser extent beta 2m, enhances IFN-gamma-induced NO production by monocytic leukaemic cells. In conclusion, these data show that d beta 2m is not able to support the formation of a stable tri-molecular MHC-I complex at physiological temperature and that d beta 2m exerts other biological functions compared to beta 2m when bound to cells.en
dc.description.sponsorshipDanish Medical Research Council; Novo Nordisk Foundation.; Serbian Ministry of Science [143029.]sr
dc.language.isoEnglishsr
dc.rightsrestrictedAccess
dc.sourceScandinavian Journal of Immunologysr
dc.titleModified Human Beta 2-Microglobulin (desLys(58)) Displays Decreased Affinity for the Heavy Chain of MHC Class I and Induces Nitric Oxide Production and Apoptosisen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractЦлаессон, МХ; Wанг, Мингјун; Буус, С; Ниссен, Могенс Х; Хеегаард, НХХ; Хархаји, Љубица М.; Ламбертх, К; Харндахл, М;
dc.citation.issue3sr
dc.citation.volume69sr
dc.citation.epage212sr
dc.type.versionpublishedVersionen
dc.citation.rankM23


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record