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dc.contributor.authorLópez-Ríos, J.-
dc.contributor.authorEsteve, Pilar-
dc.contributor.authorRuiz, José María-
dc.contributor.authorBovolenta, Paola-
dc.date.accessioned2008-11-06T12:38:59Z-
dc.date.available2008-11-06T12:38:59Z-
dc.date.issued2008-08-20-
dc.identifier.citationNeural Development 2008, 3:19en_US
dc.identifier.issn1749-8104-
dc.identifier.urihttp://hdl.handle.net/10261/8273-
dc.descriptionAdditional files: Additional File 1:SFRPCRD peptides cannot rescue the Wnt8- or Wnt5-induced over-expression phenotype. Additional File 2: Wnt8 binds to Sfrp1 and Sfrp1NTR while Sfrp1CRD binds to Frizzled 2. Additional File 3:Wnt8/Fz5 mediated activation of β-catenin transcriptional activity in dissociated embryonic retinal cells is inhibited by soluble Sfrp1 and Sfrp1NTR as well as by the Sfrp1CRD.en_US
dc.description.abstractSecreted frizzled related proteins (SFRPs) are multifunctional modulators of Wnt and BMP (Bone Morphogenetic Protein) signalling necessary for the development of most organs and the homeostasis of different adult tissues. SFRPs fold in two independent domains: the cysteine rich domain (SfrpCRD) related to the extracellular portion of Frizzled (Fz, Wnt receptors) and the Netrin module (SfrpNTR) defined by homologies with molecules such as Netrin-1, inhibitors of metalloproteinases and complement proteins. Due to its structural relationship with Fz, it is believed that SfrpCRD interferes with Wnt signalling by binding and sequestering the ligand. In contrast, the functional relevance of the SfrpNTR has been barely addressed. Results Here, we combine biochemical studies, mutational analysis and functional assays in cell culture and medaka-fish embryos to show that the Sfrp1NTR mimics the function of the entire molecule, binds to Wnt8 and antagonizes Wnt canonical signalling. This activity requires intact tertiary structure and is shared by the distantly related Netrin-1NTR. In contrast, the Sfrp1CRD cannot mirror the function of the entire molecule in vivo but interacts with Fz receptors and antagonizes Wnt8-mediated β-catenin transcriptional activity. Conclusion On the basis of these results, we propose that SFRP modulation of Wnt signalling may involve multiple and differential interactions among Wnt, Fz and SFRPs.en_US
dc.description.sponsorshipThis work was supported by grants from the Spanish MEC (BFU2004-01585 and BFU2007-61774), the Fundación la Caixa (BM04-77-0), the Fundación Mutual Madrileña (2006-0916), and Comunidad Autonoma de Madrid (CAM, P-SAL-0190-2006) to PB.en_US
dc.format.extent2435387 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isospaen_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofPublisher’s version-
dc.rightsopenAccessen_US
dc.subjectSecreted frizzled related proteinsen_US
dc.subjectSFRPsen_US
dc.subjectWnt ligandsen_US
dc.titleThe Netrin-related domain of Sfrp1 interacts with Wnt ligands and antagonizes their activity in the anterior neural plateen_US
dc.typeArtículoen_US
dc.identifier.doi10.1186/1749-8104-3-19-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1186/1749-8104-3-19en_US
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