Introduction

The retina of the eye in vertebrates is an extension of the brain, formed embryonically from neural tissue and connected to the brain through the optic nerve. The retina contains five types of neurons, including rod and cone photoreceptors, horizontal cells, bipolar cells, amacrine cells, and retinal ganglion cells. Rods and cones convert light into electrical signal that is transmitted from bipolar cells to retinal ganglion cells and then to the brain, forming the conventional excitatory neural pathway. This signaling pathway, shaped by lateral inhibition provided by horizontal cells and amacrine cells, generates image-forming vision. In addition, a subset of retinal ganglion cells expresses the melanopsin photopigment that directly responds to visible light. The intrinsically photosensitive retinal ganglion cells (ipRGCs) project to the midbrain that control pupil reflex and circadian rhythms (non-image-forming visual responses). ipRGCs also project back to the outer retina, forming a retrograde intra-retinal signaling pathway. Moreover, retinal neurodegeneration and cell death are associated with retinitis pigmentosa, diabetic retinopathy, retinopathy of prematurity, glaucoma, myopia, and Parkinson's disease, which causes low vision and even blindness. Currently, there are no cures for those diseases.

Research goal

To understand how retinal neurons develop and function under normal conditions and how they degenerate and become dysfunctional under diseased conditions. 

Research projects 

Impact

The broader impact of the work will advance the understanding of the development and function of retinal neurons and enable the rational discovery of new preventive, therapeutic interventions to combat eye disorders.  

Research support

National Institute of Health (National Eye Institute)

Mid-West Eyebanks

Research Excellence Fund (Oakland University)