Preservation of outer retina and its synaptic connectivity following subretinal injections of human RPE cells in the Royal College of Surgeons rat

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Título: Preservation of outer retina and its synaptic connectivity following subretinal injections of human RPE cells in the Royal College of Surgeons rat
Autor/es: Pinilla Lozano, Isabel | Cuenca, Nicolás | Sauvé, Yves | Wang, Shaomei | Lund, Raymond D.
Grupo/s de investigación o GITE: Neurobiología del Sistema Visual y Terapia Génica de Enfermedades Neurodegenerativas
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Biotecnología
Palabras clave: Transplant | Photoreceptors | Immunocytochemistry | Cell therapy | Retinitis pigmentosa
Área/s de conocimiento: Oftalmología
Fecha de publicación: 14-jun-2007
Editor: Elsevier
Cita bibliográfica: PINILLA LOZANO, Isabel, et al. "Preservation of outer retina and its synaptic connectivity following subretinal injections of human RPE cells in the Royal College of Surgeons rat". Experimental Eye Research. Vol. 85, Issue 3 (Sept. 2007). ISSN 0014-4835, pp. 381-392
Resumen: We have examined how transplantation of an RPE cell line to the subretinal space of RCS rats affects the distribution of synaptic connectivity markers in the outer plexiform layer of the retina. Using markers of pre- and post-synaptic profiles (bassoon and synaptophysin as presynaptic markers and mGluR6 for postsynaptic profiles) we found that the normal orderly patterns seen between photoreceptors and rod and ON-cone bipolar cells were severely disrupted in dystrophic rats. In areas in which injected cells preserved photoreceptors, more normally appearing pairing of pre- and post-synaptic markers was seen for both rods and cones. The degree of normality correlated with the amount of photoreceptor rescue. The secondary changes that are normally seen in bipolar and horizontal cells were prevented by the photoreceptor preservation. ERG recordings in the animals subsequently studied morphologically showed that both a- and b-waves could be rescued by grafting, albeit with lower amplitudes than normal. Together these anatomical and physiological studies indicate that besides the integrity of outer nuclear layer cells and phototransduction processes, relay circuitry through the outer retina was rescued by cell grafts.
Patrocinador/es: This work was supported by NIH (EY14038), Wynn Foundation, Lincy Foundation and FFB. Dr. Pinilla and Dr. Cuenca were supported by grants from the Spanish Government (FIS BA03/0016, PI042399 and BFU2006-00957/BFI), ONCE and FUNDALUCE. Dr. Lund is a recipient of a Research to Prevent Blindness Senior Scientific Investigator Award.
URI: http://hdl.handle.net/10045/13045
ISSN: 0014-4835 (Print) | 1096-0007 (Online)
DOI: 10.1016/j.exer.2007.06.002
Idioma: eng
Tipo: info:eu-repo/semantics/article
Revisión científica: si
Versión del editor: http://dx.doi.org/10.1016/j.exer.2007.06.002
Aparece en las colecciones:INV - NEUROVIS - Artículos de Revistas

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