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Gene delivery into mouse retinal ganglion cells by in utero electroporation

AutorGarcía-Frigola, Cristina; Carreres, María Isabel; Vegar, Celia; Herrera, Eloisa
Fecha de publicación17-sep-2007
EditorBioMed Central
CitaciónBMC Developmental Biology 7(103):(2007)
Resumen[Background] The neural retina is a highly structured tissue of the central nervous system that is formed by seven different cell types that are arranged in layers. Despite much effort, the genetic mechanisms that underlie retinal development are still poorly understood. In recent years, largescale genomic analyses have identified candidate genes that may play a role in retinal neurogenesis, axon guidance and other key processes during the development of the visual system. Thus, new and rapid techniques are now required to carry out high-throughput analyses of all these candidate genes in mammals. Gene delivery techniques have been described to express exogenous proteins in the retina of newborn mice but these approaches do not efficiently introduce genes into the only retinal cell type that transmits visual information to the brain, the retinal ganglion cells (RGCs).
[Results] Here we show that RGCs can be targeted for gene expression by in utero electroporation of the eye of mouse embryos. Accordingly, using this technique we have monitored the morphology of electroporated RGCs expressing reporter genes at different developmental stages, as well as their projection to higher visual targets.
[Conclusion] Our method to deliver ectopic genes into mouse embryonic retinas enables us to follow the course of the entire retinofugal pathway by visualizing RGC bodies and axons. Thus, this technique will permit to perform functional studies in vivo focusing on neurogenesis, axon guidance, axon projection patterning or neural connectivity in mammals.
Descripción10 páginas, 5 figuras.
Versión del editorhttp://dx.doi.org/10.1186/1471-213X-7-103
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