Retinal defects in mice lacking the autism-associated gene Engrailed-2

摘要

Defective cortical processing of visual stimuli and altered retinal function have been described in autism spectrum disorder (ASD) patients. In keeping with these findings, anatomical and functional defects have been found in the visual cortex and retina of mice bearing mutations for ASD-associated genes. Here we sought to investigate the anatomy and function of the adult retina of Engrailed 2 knockout (En2(-/-)) mice, a model for ASD. Our results showed that En2 is expressed in all three nuclear layers of the adult retina. When compared to age-matched En2(+/+) controls, En2(-/-) adult retinas showed a significant decrease in the number of calbindin(+) horizontal cells, and a significant increase in calbindin(+ )amacrine/ganglion cells. The total number of ganglion cells was not altered in the adult En2(-/-) retina, as shown by Brn3a(+) cell counts. In addition, En2(-/-) adult mice showed a significant reduction of photoreceptor (rhodopsin) and bipolar cell (Pcp2, PKC alpha) markers. Functional defects were also present in the retina of En2 mutants, as indicated by electroretinogram recordings showing a significant reduction in both a-wave and b-wave amplitude in En2(-/-) mice as compared to controls. These data show for the first time that anatomical and functional defects are present in the retina of the En2 ASD mouse model. (C) 2019 IBRO. Published by Elsevier Ltd. All rights reserved.