Publication: Brn3a as a marker of retinal ganglion cells: qualitative and quantitative time course studies in naïve and optic nerve–injured retinas
Authors
Jiménez López, Manuel ; Sobrado Calvo, Paloma ; Nieto López, Leticia ; Cánovas Martínez, Isabel ; Vidal Sanz, Manuel ; Agudo, Marta ; Salinas Navarro, Manuel Ángel ; Nadal-Nicolás, Francisco Manuel
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Publisher
Association for Research in Vision and Ophthalmology
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DOI
https://doi.org/10.1167/iovs.08-3267
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info:eu-repo/semantics/article
Description
© 2009 The Association for Research in Vision and Ophthalmology, Inc. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
This document is the Published Manuscript version of a Published Work that appeared in final form in Investigative Ophthalmology & Visual Science. To access the final edited and published work see https://doi.org/10.1167/iovs.08-3267
Abstract
Purpose. To characterize Brn3a expression in adult albino rat retinal ganglion cells (RGCs) in naïve animals and in animals subjected to complete intraorbital optic nerve transection (IONT) or crush (IONC).
methods. Rats were divided into three groups, naïve, IONT, and IONC. Two-, 5-, 9-, or 14-day postlesion (dpl) retinas were examined for immunoreactivity for Brn3a. Before the injury, the RGCs were labeled with Fluorogold (FG; Fluorochrome, Corp. Denver, CO). Brn3a retinal expression was also determined by Western blot analysis. The proportion of RGCs double labeled with Brn3a and FG was determined in radial sections. The temporal course of reduction in Brn3a+ RGCs and FG+ RGCs induced by IONC or IONT was assessed by quantifying, in the same wholemounts, the number of surviving FG-labeled RGCs and Brn3a+RGCs at the mentioned time points. The total number of FG+RGCs was automatically counted in naïve and injured retinas (2 and 5 dpl) or estimated by manual quantification in retinas processed at 9 and 14 dpl. All Brn3a immunopositive RGCs were counted using an automatic routine specifically developed for this purpose. This protocol allowed, as well, the investigation of the spatial distribution of these neurons.
results. Brn3a+ cells were only present in the ganglion cell layer and showed a spatial distribution comparable to that of FG+ cells. In the naïve retinal wholemounts the mean (mean ± SEM; n = 14) total number of FG+RGCs and Brn3a+RGCs was 80,251 ± 2,210 and 83,449 ± 4,541, respectively. Whereas in the radial sections, 92.2% of the FG+RGCs were also Brn3a+, 4.4% of the RGCs were Brn3a+FG− and 3.4% were FG+Brn3a−. Brn3a expression pattern was maintained in injured RGCs. The temporal course of Brn3a+RGC and FG+RGC loss induced by IONC or IONT followed a similar trend, but Brn3a+RGCs loss was detected earlier than that of FG+RGCs. Independent of the marker used to detect the RGCs, it was observed that their loss was quicker and more severe after IONT than after IONC.
conclusions. Brn3a can be used as a reliable, efficient ex vivo marker to identify and quantify RGCs in control and optic nerve–injured retinas.
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Citation
Investigative Ophthalmology & Visual Science, 2009, Vol.50, Issue 8, pp. 3860-3868
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