Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells

Shane P. D'Souza, David I. Swygart, Sophia R. Wienbar, Brian A. Upton, Kevin X. Zhang, Robert D. Mackin, Anna K. Casasent, Melanie A. Samuel, Gregory W. Schwartz, Richard A. Lang*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Obtaining a parts list of the sensory components of the retina is vital to understand the effects of light in behavior, health, and disease. Rods, cones, and intrinsically photosensitive retinal ganglion cells (ipRGCs) are the best described photoreceptors in the mammalian retina, but recent functional roles have been proposed for retinal neuropsin (Opn5)—an atypical opsin. However, little is known about the pattern of Opn5 expression in the retina. Using cre (Opn5cre) and cre-dependent reporters, we uncover patterns of Opn5 expression and find that Opn5 is restricted to retinal ganglion cells (RGCs). Opn5-RGCs are nonhomogenously distributed through the retina, with greater densities of cells located in the dorsotemporal quadrant. In addition to the local topology of these cells, using cre-dependent AAV viral tracing, we surveyed their central targets and found that they are biased towards image-forming and image-stabilizing regions. Finally, molecular and electrophysiological profiling reveal that Opn5-RGCs comprise previously defined RGC types that respond optimally to edges and object-motion (F-mini-ONs, HD2, HD1, LEDs, ooDSRGCs, etc.). Together, these data describe the second collection of RGCs that express atypical opsins in the mouse, and expand the roles of image-forming cells in retinal physiology and function.

Original languageEnglish (US)
Pages (from-to)1247-1262
Number of pages16
JournalJournal of Comparative Neurology
Volume530
Issue number8
DOIs
StatePublished - Jun 2022

Funding

We thank Paul Speeg for excellent mouse colony management, Dr. Tudor Badea for gifting us anti‐Tusc5 antibody (SCB) aliquots. We thank Allie Pendery for reviewing this manuscript. This work was supported by NIH grants NEI R01 EY027711 and EY027077 to R.A.L., NIH DP2 EY026770 to G.W.S., F31 EY030737 to S.R.W., F31 EY030344 to D.I.S., and the Albert J. Ryan Predoctoral Fellowship to S.D. This work was also supported by funds from the Goldman Chair of the Abrahamson Pediatric Eye Institute at CCHMC.

ASJC Scopus subject areas

  • General Neuroscience

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