Loss of Outer Retinal Neurons and Circuitry Alterations in the DBA/2J Mouse


Autoria(s): Fernández Sánchez, Laura; Pérez de Sevilla Müller, Luis; Brecha, Nicholas C.; Cuenca, Nicolás
Contribuinte(s)

Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología

Neurobiología del Sistema Visual y Terapia de Enfermedades Neurodegenerativas (NEUROVIS)

Data(s)

01/10/2014

01/10/2014

24/09/2014

Resumo

Purpose. The DBA/2J mouse line develops essential iris atrophy, pigment dispersion, and glaucomatous age-related changes, including an increase of IOP, optic nerve atrophy, and retinal ganglion cell (RGC) death. The aim of this study was to evaluate possible morphological changes in the outer retina of the DBA/2J mouse concomitant with disease progression and aging, based on the reduction of both the a- and b-waves and photopic flicker ERGs in this mouse line. Methods. Vertically sectioned DBA/2J mice retinas were evaluated at 3, 8, and 16 months of age using photoreceptor, horizontal, and bipolar cell markers. Sixteen-month-old C57BL/6 mice retinas were used as controls. Results. The DBA/2J mice had outer retinal degeneration at all ages, with the most severe degeneration in the oldest retinas. At 3 months of age, the number of photoreceptor cells and the thickness of the OPL were reduced. In addition, there was a loss of horizontal and ON-bipolar cell processes. At 8 months of age, RGC degeneration occurred in patches, and in the outer retina overlying these patches, cone morphology was impaired with a reduction in size as well as loss of outer segments and growth of horizontal and bipolar cell processes into the outer nuclear layer. At 16 months of age, connectivity between photoreceptors and horizontal and bipolar cell processes overlying these patches was lost. Conclusions. Retinal degeneration in DBA/2J mice includes photoreceptor death, loss of bipolar and horizontal cell processes, and loss of synaptic contacts in an aging-dependent manner.

Supported by grants from the Spanish Ministry of Economy and Competitivity-FEDER (BFU2012-36845), Instituto de Salud Carlos III (RETICS RD12/0034/0010), National Organization of Spanish Blind (ONCE1-13I), FUNDALUCE (Foundation for Fighting Blindness, Spain), National Institutes of Health EY04067 (NCB), National Institute of Diabetes and Digestive and Kidney Diseases P30 DK41301 (University of California Los Angeles Cure Center Core), and a Department of Veterans Affairs (VA) Merit Review (NCB). NCB is a VA Career Research Scientist.

Identificador

Investigative Ophthalmology & Visual Science. 2014, 55(9): 6059-6072. doi:10.1167/iovs.14-14421

0146-0404 (Print)

1552-5783 (Online)

http://hdl.handle.net/10045/40805

10.1167/iovs.14-14421

Idioma(s)

eng

Publicador

Association for Research in Vision and Ophthalmology (ARVO)

Relação

http://dx.doi.org/10.1167/iovs.14-14421

Direitos

© 2014 by Association for Research in Vision and Ophthalmology

info:eu-repo/semantics/openAccess

Palavras-Chave #Photoreceptor #Horizontal cell #Bipolar cell #Synaptic triad #Retinal degeneration #Glaucoma #Biología Celular
Tipo

info:eu-repo/semantics/article