Publication: Brain derived neurotrophic factor maintains Brn3a expression in axotomized rat retinal ganglion cells
| dc.contributor.author | Sánchez Migallón, María del Cielo | |
| dc.contributor.author | Nadal-Nicolás, Francisco Manuel | |
| dc.contributor.author | Jiménez López, Manuel | |
| dc.contributor.author | Sobrado Calvo, Paloma | |
| dc.contributor.author | Vidal Sanz, Manuel | |
| dc.contributor.author | Agudo Barriuso, Marta | |
| dc.contributor.department | Oftalmología, Optometría, Otorrinolaringología y Anatomía Patológica | |
| dc.contributor.other | Facultades de la UMU::Facultad de Medicina | |
| dc.date.accessioned | 2026-01-27T08:38:21Z | |
| dc.date.available | 2026-01-27T08:38:21Z | |
| dc.date.copyright | © 2011 Elsevier Ltd. | |
| dc.date.issued | 2009-08-16 | |
| dc.description.abstract | The transcription factor Brn3a has been reported to be a good marker for adult rat retinal ganglion cells in control and injured retinas. However, it is still unclear if Brn3a expression declines progressively by the injury itself or otherwise its expression is maintained in retinal ganglion cells that, though being injured, are still alive, as might occur when assessing neuroprotective therapies. Therefore, we have automatically quantified the whole population of surviving Brn3a positive retinal ganglion cells in retinas subjected to intraorbital optic nerve transection and treated with either brain derived neurotrophic factor or vehicle. Brain derived neurotrophic factor is known to delay retinal ganglion cell death after axotomy. Thus, comparison of both groups would inform of the suitability of Brn3a as a retinal ganglion cell marker when testing neuroprotective molecules. As internal control, retinal ganglion cells were, as well, identified in all retinas by retrogradely tracing them with fluorogold. Our data show that at all the analyzed times post-lesion, the numbers of Brn3a positive retinal ganglion cells and of fluorogold positive retinal ganglion cells are significantly higher in the brain derived neurotrophic factor-treated retinas compared to the vehicle-treated ones. Moreover, detailed isodensity maps of the surviving Brn3a positive retinal ganglion cells show that a single injection of brain derived neurotrophic factor protects retinal ganglion cells throughout the entire retina. In conclusion, Brn3a is a reliable retinal ganglion cell marker that can be used to accurately measure the potential effect of a given neuroprotective therapy. | |
| dc.format | application/pdf | |
| dc.format.extent | 8 | |
| dc.identifier.citation | Vision Res. 2009 Nov;49(23):2808-25 | |
| dc.identifier.doi | https://doi.org/10.1016/j.exer.2011.02.001 | |
| dc.identifier.issn | 0014-4835 | |
| dc.identifier.uri | http://hdl.handle.net/10201/194170 | |
| dc.language | eng | |
| dc.publisher | Elsevier | |
| dc.relation | This work was supported by research grants from Fundación Séneca 04446/GERM/07; Spanish Ministry of Education and Science SAF-22010-10385; Spanish Ministry of Science and Innovation and ISCIII-FEDER: PI07/0225; PI10/00187, PI10/01496 and Red Temática de Investigación Cooperativa en Oftalmología RD07/0062/0001. | |
| dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0014483511000352 | |
| dc.rights.accessRights | info:eu-repo/semantics/restrictedAccess | |
| dc.subject | RGC | |
| dc.subject | Axotomy | |
| dc.subject | Survival | |
| dc.subject | Brn3a | |
| dc.subject | BDNF | |
| dc.subject | Spatial distribution | |
| dc.subject.ods | Objetivo 3: Salud | |
| dc.title | Brain derived neurotrophic factor maintains Brn3a expression in axotomized rat retinal ganglion cells | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dspace.entity.type | Publication | es |
| relation.isAuthorOfPublication | ba9bf053-48ec-4e39-93ac-ffcbaf10fc0f | |
| relation.isAuthorOfPublication | ce26a072-5090-4cfb-b469-5b9a0b5dc462 | |
| relation.isAuthorOfPublication | 8cc42adf-31e9-49c4-a5e2-476346abe217 | |
| relation.isAuthorOfPublication | 5bf27bab-9d43-4b02-a752-5513261676f6 | |
| relation.isAuthorOfPublication.latestForDiscovery | ba9bf053-48ec-4e39-93ac-ffcbaf10fc0f |
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