Publication:
Long-term effect of optic nerve axotomy on the retinal ganglion cell layer

dc.contributor.authorNadal-Nicolás, Francisco Manuel
dc.contributor.authorSobrado Calvo, Paloma
dc.contributor.authorJiménez López, Manuel
dc.contributor.authorVidal Sanz, Manuel
dc.contributor.authorAgudo Barriuso, Marta
dc.contributor.departmentOftalmología, Optometría, Otorrinolaringología y Anatomía Patológica
dc.contributor.otherFacultades de la UMU::Facultad de Medicina
dc.date.accessioned2026-01-27T08:41:05Z
dc.date.available2026-01-27T08:41:05Z
dc.date.copyright© 2015 The Association for Research in Vision and Ophthalmology, Inc.
dc.date.issued2015-09-01
dc.description.abstractPurpose: To analyze the long-term effect of optic nerve injury on retinal ganglion cells (RGCs) and melanopsin+RGCs orthotopic and displaced, and on the rest of the ganglion cell layer (GCL) cells. Methods: In adult albino rats, the left optic nerve was crushed (ONC) or transected (ONT). Injured and contralateral retinas were analyzed at increasing survival intervals (up to 15 months). To study all GCL cells and RGCs, retinas were immunodetected with Brn3a and melanopsin to identify the general RGC population (Brn3a+) and m+RGCs, and counter-stained with 4′,6-diamidino-2-phenylindole (DAPI). Brn3a+RGCs and m+RGCs displaced to the inner nuclear layer were analyzed as well. In additional retinas, glial cells in the GCL were identified with glial fibrillary acidic protein (GFAP) or Iba1, and in some retinas, Brn3a, calretinin, and γ-synuclein were immunodetected. Results: Orthotopic and displaced RGCs behave similarly within the RGC and m+RGC populations. Both lesions cause an exponential loss of RGCs (4%–1% survival at 6 months after ONC or ONT), but not of m+RGCs, whose number remains stable from 1 to 15 months (34%–44% of the initial population). γ-synuclein is expressed by RGCs and displaced amacrine cells (dACs), allowing us to confirm that axotomy does not affect the latter, and to determine that out of the approximately 217,406 cells that compose the GCL (excluding endothelia), 10% are glial cells, 50% dACs, and the remaining 40% are RGCs. Conclusions: In the GCL, only RGCs are lost after axotomy, and there are important differences in the course of loss and rate of survival between melanopsin+RGCs and the rest of RGCs.
dc.formatapplication/pdf
dc.identifier.citationInvest Ophthalmol Vis Sci. 2015 Sep;56(10):6095-112.
dc.identifier.doihttps://doi.org/10.1167/iovs.15-17195
dc.identifier.eissn1552-5783
dc.identifier.issn0146-0404
dc.identifier.urihttp://hdl.handle.net/10201/194209
dc.languageeng
dc.publisherAssociation for Research in Vision and Ophthalmology.
dc.relationSupported by grants from the Spanish Ministry of Economy and Competitiveness: ISCIII-FEDER ‘‘Una manera de hacer Europa’’ PI13/00643; SAF-2012-38328 (Madrid, Spain)
dc.relation.publisherversionhttps://iovs.arvojournals.org/article.aspx?articleid=2443691
dc.rightsAttribution 4.0 International*
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectIntrinsically photosensitive retinal ganglion cells
dc.subjectTopography
dc.subjectBrn3a
dc.subjectMelanopsin
dc.subjectDisplaced amacrine cells
dc.subjectGamma synuclein
dc.subjectDisplaced retinal ganglion cells
dc.subject.odsObjetivo 3: Salud
dc.titleLong-term effect of optic nerve axotomy on the retinal ganglion cell layer
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion
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