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dc.contributor.authorChigusa, Yoshitsuguen
dc.contributor.authorTatsumi, Keijien
dc.contributor.authorKondoh, Eijien
dc.contributor.authorFujita, Koheien
dc.contributor.authorNishimura, Fumitomoen
dc.contributor.authorMogami, Harutaen
dc.contributor.authorKonishi, Ikuoen
dc.contributor.alternative巽, 啓司ja
dc.date.accessioned2014-03-10T02:33:15Z-
dc.date.available2014-03-10T02:33:15Z-
dc.date.issued2012-10-
dc.identifier.issn0021-972X-
dc.identifier.urihttp://hdl.handle.net/2433/182957-
dc.description.abstractobjective: The objective of the study was to assess LOX-1 expression and Nrf2 activation in preeclamptic placentas and to manifest their physiological roles in preeclampsia. Methods: Expression and regulation of LOX-1, HO-1, and Nrf2 were evaluated by real-time quantitative RT-PCR and Western blotting. The functions of LOX-1 and Nrf2 were examined using an anti-LOX-1 antibody and Nrf2 activator in JAR, a choriocarcinoma cell line, and placental explants. Results: Both LOX-1 expression and Nrf2 activation were significantly decreased in preeclamptic placentas compared with normal controls. A significant decrease in LOX-1 mRNA was found in placental explant cultures under hypoxic conditions. Activation of Nrf2 up-regulated HO-1 in both the JAR cells and placental explants. Furthermore, oxLDL increased HO-1 mRNA, whereas the blockade of LOX-1 inhibited the increase of HO-1 mRNA in JAR cells. Conclusion: Decreasing LOX-1 expression in preeclamptic placenta may contribute to high oxLDL concentration, low Nrf2 activation, and low HO-1 expression. These findings provide novel insights into the crucial role of LOX-1 and Nrf2 in the pathogenesis of preeclampsia.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherEndocrine Societyen
dc.rights© 2012 by The Endocrine Societyen
dc.subject.meshAdulten
dc.subject.meshAnoxia/metabolismen
dc.subject.meshAnoxia/pathologyen
dc.subject.meshAntioxidants/metabolismen
dc.subject.meshCell Line, Tumoren
dc.subject.meshChoriocarcinomaen
dc.subject.meshChorionic Villi/metabolismen
dc.subject.meshChorionic Villi/pathologyen
dc.subject.meshFemaleen
dc.subject.meshHeme Oxygenase-1/geneticsen
dc.subject.meshHeme Oxygenase-1/metabolismen
dc.subject.meshHumansen
dc.subject.meshLipoproteins, LDL/metabolismen
dc.subject.meshNF-E2-Related Factor 2/geneticsen
dc.subject.meshNF-E2-Related Factor 2/metabolismen
dc.subject.meshPlacenta/metabolismen
dc.subject.meshPlacenta/pathologyen
dc.subject.meshPre-Eclampsia/metabolismen
dc.subject.meshPre-Eclampsia/pathologyen
dc.subject.meshPregnancyen
dc.subject.meshRNA, Messenger/metabolismen
dc.subject.meshScavenger Receptors, Class E/geneticsen
dc.subject.meshScavenger Receptors, Class E/metabolismen
dc.subject.meshUterine Neoplasmsen
dc.titleDecreased lectin-like oxidized LDL receptor 1 (LOX-1) and low Nrf2 activation in placenta are involved in preeclampsia.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA00695484-
dc.identifier.jtitleThe Journal of clinical endocrinology and metabolismen
dc.identifier.volume97-
dc.identifier.issue10-
dc.identifier.spageE1862-
dc.identifier.epageE1870-
dc.relation.doi10.1210/jc.2012-1268-
dc.textversionpublisher-
dc.identifier.pmid22791762-
dcterms.accessRightsopen access-
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