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dc.contributor.authorBrohus, Men_US
dc.contributor.authorGorbunova, Ven_US
dc.contributor.authorFaulkes, CGen_US
dc.contributor.authorOvergaard, MTen_US
dc.contributor.authorConover, CAen_US
dc.date.accessioned2016-09-15T13:29:16Z
dc.date.available2015-12-04en_US
dc.date.issued2015en_US
dc.date.submitted2016-09-13T20:32:57.159Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/15384
dc.description.abstractNaked mole-rats (Heterocephalus glaber) (NMRs) are the longest living rodents known. They show negligible senescence, and are resistant to cancers and certain damaging effects associated with aging. The insulin-like growth factors (IGFs) have pluripotent actions, influencing growth processes in virtually every system of the body. They are established contributors to the aging process, confirmed by the demonstration that decreased IGF signaling results in life-extending effects in a variety of species. The IGFs are likewise involved in progression of cancers by mediating survival signals in malignant cells. This report presents a full characterization of the IGF system in the NMR: ligands, receptors, IGF binding proteins (IGFBPs), and IGFBP proteases. A particular emphasis was placed on the IGFBP protease, pregnancy-associated plasma protein-A (PAPP-A), shown to be an important lifespan modulator in mice. Comparisons of IGF-related genes in the NMR with human and murine sequences indicated no major differences in essential parts of the IGF system, including PAPP-A. The protease was shown to possess an intact active site despite the report of a contradictory genome sequence. Furthermore, PAPP-A was expressed and translated in NMRs cells and retained IGF-dependent proteolytic activity towards IGFBP-4 and IGF-independent activity towards IGFBP-5. However, experimental data suggest differential regulatory mechanisms for PAPP-A expression in NMRs than those described in humans and mice. This overall description of the IGF system in the NMR represents an initial step towards elucidating the complex molecular mechanisms underlying longevity, and how these animals have evolved to ensure a delayed and healthy aging process.en_US
dc.format.extente0145587 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofPLoS Oneen_US
dc.rightsCC-BY
dc.subjectAgingen_US
dc.subjectAnimalsen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectInsulin-Like Growth Factor Binding Protein 4en_US
dc.subjectInsulin-Like Growth Factor Binding Protein 5en_US
dc.subjectMaleen_US
dc.subjectMiceen_US
dc.subjectMole Ratsen_US
dc.subjectPregnancy-Associated Plasma Protein-Aen_US
dc.subjectRatsen_US
dc.subjectSomatomedinsen_US
dc.subjectSpecies Specificityen_US
dc.titleThe Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat.en_US
dc.typeArticle
dc.rights.holder© 2015 Brohus et al.
dc.identifier.doi10.1371/journal.pone.0145587en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/26694858en_US
pubs.issue12en_US
pubs.notesNo embargoen_US
pubs.publication-statusPublished onlineen_US
pubs.volume10en_US
dcterms.dateAccepted2015-12-04en_US


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