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dc.contributor.authorPuelles, Luis
dc.contributor.authorMorales Delgado, N.
dc.contributor.authorMerchán, P.
dc.contributor.authorCastro Robles, Beatriz
dc.contributor.authorMartínez de la Torre, M.
dc.contributor.authorDíaz, C.
dc.contributor.authorFerran, J. L.
dc.date.accessioned2017-01-18T11:16:57Z
dc.date.available2017-01-18T11:16:57Z
dc.date.issued2016
dc.identifier.issn1863-2653
dc.identifier.urihttp://hdl.handle.net/10459.1/59022
dc.description.abstractThe telencephalic subpallium is the source of various GABAergic interneuron cohorts that invade the pallium via tangential migration. Based on genoarchitectonic studies, the subpallium has been subdivided into four major domains: striatum, pallidum, diagonal area and preoptic area (Puelles et al. 2013; Allen Developing Mouse Brain Atlas), and a larger set of molecularly distinct progenitor areas (Flames et al. 2007). Fate mapping, genetic lineage-tracing studies, and other approaches have suggested that each subpallial subdivision produces specific sorts of inhibitory interneurons, distinguished by differential peptidic content, which are distributed tangentially to pallial and subpallial target territories (e.g., olfactory bulb, isocortex, hippocampus, pallial and subpallial amygdala, striatum, pallidum, septum). In this report, we map descriptively the early differentiation and apparent migratory dispersion of mouse subpallial somatostatin-expressing (Sst) cells from E10.5 onward, comparing their topography with the expression patterns of the genes Dlx5, Gbx2, Lhx7-8, Nkx2.1, Nkx5.1 (Hmx3), and Shh, which variously label parts of the subpallium. Whereas some experimental results suggest that Sst cells are pallidal, our data reveal that many, if not most, telencephalic Sst cells derive from de diagonal area (Dg). Sst-positive cells initially only present at the embryonic Dg selectively populate radially the medial part of the bed nucleus striae terminalis (from paraseptal to amygdaloid regions) and part of the central amygdala; they also invade tangentially the striatum, while eschewing the globus pallidum and the preoptic area, and integrate within most cortical and nuclear pallial areas between E10.5 and E16.5.ca_ES
dc.description.sponsorshipThis work was funded by the Spanish Ministry of Science and Innovation grant BFU2008-04156, and SENECA Foundation contract 0458/GERM/06-10891 to L.P.; and the Local Government of Castilla-La Mancha grant PII1I09-0065-8194 to C.D. Infrastructure support provided by the University of Murcia and Castilla-La Mancha is also acknowledged.ca_ES
dc.language.isoengca_ES
dc.publisherSpringer Berlin Heidelbergca_ES
dc.relationMICINN/PN2008-2011/BFU2008-04156
dc.relation.isformatofReproducció del document publicat a https://doi.org/10.1007/s00429-015-1086-8ca_ES
dc.relation.ispartofBrain Structure and Function, 2016, vol. 221, núm. 6, p. 3027-3065ca_ES
dc.rightscc-by (c) Puelles, Luis et al., 2015ca_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectForebrain interneuronsca_ES
dc.subjectSecondary prosencephalonca_ES
dc.subjectSubpalliumca_ES
dc.subjectPallidumca_ES
dc.titleRadial and tangential migration of telencephalic somatostatin neurons originated from the mouse diagonal areaca_ES
dc.typearticleca_ES
dc.type.versionpublishedVersionca_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_ES
dc.identifier.doihttps://doi.org/10.1007/s00429-015-1086-8


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cc-by (c) Puelles, Luis et al., 2015
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