Regulation of advanced glycation end product (AGE) receptors and apoptosis by AGEs in osteoblast-like cells

cic.isFulltexttruees
cic.isPeerReviewedtruees
cic.lugarDesarrolloUniversidad Nacional de La Plata es
cic.versioninfo:eu-repo/semantics/submittedVersiones
dc.date.accessioned2016-12-12T16:51:46Z
dc.date.available2016-12-12T16:51:46Z
dc.identifier.urihttps://digital.cic.gba.gob.ar/handle/11746/4960
dc.titleRegulation of advanced glycation end product (AGE) receptors and apoptosis by AGEs in osteoblast-like cellsen
dc.typeDocumento de conferenciaes
dcterms.abstractAdvanced glycation end products (AGEs) have been proposed as the pathological mechanisms underlying diabetic chronic complications. They may also play a role in the pathogenesis of diabetic osteopenia, although their mechanisms of action remain unclear. We investigated the protein (immunofluorescence) and gene expression (realtime RT-PCR) of two receptors for AGEs, RAGE and galectin-3, as well as their regulation by AGEs, and the apoptotic effect on osteoblast-like cells (UMR106 and MC3T3E1) in culture. AGEs up-regulated the expression of RAGE and galectin-3 in both cells lines. These effects were accompanied by an increase in the corresponding mRNA in the non-tumoral MC3T3E1 but not in the osteosarcoma UMR106 cells. Finally, we demonstrated that a 24 h exposure to AGEs induced apoptosis in both cell lines. Thus, AGEs-receptors may play important roles in the bone alterations described in aging and diabetic patients.en
dcterms.creator.authorMercer, Nataliaes
dcterms.creator.authorAhmed, Hafizes
dcterms.creator.authorEtcheverry, Susana B.es
dcterms.creator.authorVasta, Gerardo R.es
dcterms.creator.authorCortizo, Ana Maríaes
dcterms.extent8 p.es
dcterms.isPartOf.issuevol. 306es
dcterms.isPartOf.seriesMolecular and Cellular Biochemistryes
dcterms.issued2007
dcterms.languageIngléses
dcterms.licenseAttribution 4.0 International (BY 4.0)es
dcterms.subjectAdvanced glycation end productsen
dcterms.subjectRAGEen
dcterms.subjectGalectin-3en
dcterms.subjectOsteoblastsen
dcterms.subjectApoptosisen
dcterms.subjectAGE-receptorsen
dcterms.subjectRegulationen
dcterms.subject.materiaCiencias Químicases
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