Rod bipolar cells receive cone photoreceptor inputs through both invaginating synapses and flat contacts in the mouse and guinea pig retinas

Author:

Xiao Jiayi1,Wang Fenglan1,Yang Qingwen1,Zhong Wenhui1,Zang Keduo1,Tan Hang1,Lin Xin12,Rao Bilin12,Gao Meiling12,Zhang Jun123ORCID

Affiliation:

1. Laboratory of Retinal Physiology and Disease, School of Ophthalmology and Optometry and Eye Hospital Wenzhou Medical University Wenzhou China

2. State Key Laboratory of Ophthalmology, Optometry and Vision Science, Eye Hospital Wenzhou Medical University Wenzhou China

3. National Clinical Research Center for Ocular Diseases, Eye Hospital Wenzhou Medical University Wenzhou China

Abstract

AbstractThe light pathways are segregated into rod and cone pathways in which rods synapse with rod bipolar cells (RBCs), while cones contact cone bipolar cells (CBCs). However, previous studies found that cones can make synapse with RBCs (cone–RBC synapses) and rods can contact OFF CBC in primate and rabbit retinas. Recently, such cone–RBC synapses have been reported physiologically and morphologically in the mouse retina. Nevertheless, the precise subcellular evidence to determine whether it is the invaginating synapse or the flat contact remains absent. This is due to a lack of immunochemically verified ultrastructural data. Here, we investigated the precise expression of protein kinase C alpha (PKCα) using pre‐embedding immunoelectron microscopy (immuno‐EM) with a monoclonal antibody against PKCα, a biomarker for the RBCs. We determined the nanoscale localization of PKCα in the outer plexiform layer of the mouse and guinea pig retinas. Our results demonstrate the existence of both the direct invaginating synapse and the basal/flat contact of the cone–RBCs, providing for the first time immunochemically verified ultrastructural evidence for the cone–RBC synapse in the mouse and guinea pig retinas. These results suggest that the cross talk between cone and rod pathways is much more extensive than previously assumed.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Neuroscience

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