Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/45513
Campo DC Valoridioma
dc.contributor.authorAlfayate, M. C.
dc.contributor.authorSantos, E.
dc.contributor.authorYanes, C.
dc.contributor.authorCasañas, N.
dc.contributor.authorViñoly, R.
dc.contributor.authordel Mar Romero-Aleman, Maria
dc.contributor.authorMonzón-Mayor, Maximina
dc.contributor.otherROMERO-ALEMAN, MARIA DEL MAR
dc.contributor.otherAlfayate Casanas, Maria del Carmen
dc.contributor.otherMonzon-Mayor, Maximina
dc.date.accessioned2018-11-22T10:26:06Z-
dc.date.available2018-11-22T10:26:06Z-
dc.date.issued2011
dc.identifier.issn0302-766X
dc.identifier.urihttp://hdl.handle.net/10553/45513-
dc.description.abstractSpontaneous regrowth of the axons of retinal ganglion cells (RGC) occurs after unilateral optic nerve transection (ONT) in the lizard Gallotia galloti. We have performed an immunohistochemical and ultrastructural study of the conus papillaris (CP) of this lizard during ontogeny and after ONT in order to characterize its cell subpopulations, innervation and putative blood-brain barrier (BBB) and to evaluate changes occurring throughout regeneration. Proliferating PCNA(+) cells were abundant between embryonic stage 33 (E33) and hatching. From E33, we observed Pax2(+)/GS(+) glial cells in the primitive CP, which became increasingly pigmented and vascularised from E35. Conal astrocytes coexpressing Pax2 with vimentin and/or GFAP were identified from E37-E38. GluT-1(+)/LEA(+)/Pax2(-) endothelial cells (ECs) formed a continuous endothelium with tight junctions and luminal and abluminal microfolds. In adults, the peripheral blood vessels showed a thinner calibre, stronger GluT-1 staining and more abundant microfolds than those of the central CP indicating the higher specialization involved during transport within the former. Occasional pericytes, abundant Pax2(+) pigment cells, LEA(+) microglia/macrophages, unmyelinated Tuj1(+) nerve fibres and SV2(+) synaptic vesicles were also observed in the perivascular zone. After ONT, the expression of GluT-1 and p75(NTR) persisted in ECs, suggesting the preservation/early recovery of the BBB. Relevant ultrastructural alterations were observed at 0.5 months postlesion, although, by 3 months, the CP had recovered the ultrastructure of controls indicating tissue recovery. Abnormal newly formed blood vessels had developed in the CP-optic nerve junction. Thus, the CP is a central nervous system structure whose regenerating capacity might be key for the nutritional support of regenerating RGCs in G. galloti.
dc.publisher0302-766X
dc.relation.ispartofCell and Tissue Research
dc.sourceCell And Tissue Research[ISSN 0302-766X],v. 344 (1), p. 63-83
dc.subject.otherBlood-Brain-Barrier
dc.subject.otherAstrocyte Precursor Cells
dc.subject.otherElectron-Microscopic Observations
dc.subject.otherNeurotrophin Receptor P75Ntr
dc.subject.otherCapillary Endothelial-Cells
dc.subject.otherGrowth-Factor Receptors
dc.subject.otherFine-Structure
dc.subject.otherPecten Oculi
dc.subject.otherGlial-Cells
dc.subject.otherQuail Retina
dc.titleOntogeny of the conus papillaris of the lizard Gallotia galloti and cellular response following transection of the optic nerve: An immunohistochemical and ultrastructural study
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1007/s00441-011-1128-3
dc.identifier.scopus79953810282-
dc.identifier.isi000288754300007
dcterms.isPartOfCell And Tissue Research
dcterms.sourceCell And Tissue Research[ISSN 0302-766X],v. 344 (1), p. 63-83
dc.contributor.authorscopusid6506345277
dc.contributor.authorscopusid35084324600
dc.contributor.authorscopusid7004187530
dc.contributor.authorscopusid46760925000
dc.contributor.authorscopusid37115097800
dc.contributor.authorscopusid6506533545
dc.contributor.authorscopusid36793900900
dc.description.lastpage83
dc.description.firstpage63
dc.relation.volume344
dc.type2Artículoes
dc.identifier.wosWOS:000288754300007
dc.contributor.daisngid3490643
dc.contributor.daisngid2816094
dc.contributor.daisngid675718
dc.contributor.daisngid4120745
dc.contributor.daisngid2476119
dc.contributor.daisngid1157526
dc.contributor.daisngid901526
dc.identifier.investigatorRIDK-8038-2014
dc.identifier.investigatorRIDNo ID
dc.identifier.investigatorRIDNo ID
dc.contributor.wosstandardWOS:Alfayate, MC
dc.contributor.wosstandardWOS:Santos, E
dc.contributor.wosstandardWOS:Yanes, C
dc.contributor.wosstandardWOS:Casanas, N
dc.contributor.wosstandardWOS:Vinoly, R
dc.contributor.wosstandardWOS:Romero-Aleman, MD
dc.contributor.wosstandardWOS:Monzon-Mayor, M
dc.date.coverdateAbril 2011
dc.identifier.ulpgces
dc.description.sjr1,501
dc.description.jcr3,114
dc.description.sjrqQ1
dc.description.jcrqQ3
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.deptGIR IUIBS: Tecnología Médica y Audiovisual-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0002-7987-5509-
crisitem.author.orcid0000-0002-5046-508X-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameYanes Mendez, Carmen M-
crisitem.author.fullNameRomero Alemán, María Del Mar-
crisitem.author.fullNameMonzón Mayor,Maximina-
Colección:Artículos
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