AI Article Synopsis

  • The study investigates retinal neural circuitry in vertebrates, focusing on the outer plexiform layer where photoreceptors connect with bipolar and horizontal cells for visual perception.
  • It identifies Necl-1/CADM3 as a crucial factor for synapse formation between S- and S/M-opsin cones and type 4 OFF cone bipolar cells (CBCs) in the mouse retina.
  • Mice lacking Necl-1 displayed abnormal synapse positioning and impaired visual responses, indicating that Necl-1 plays a key role in facilitating OFF pathways for short-wavelength light processing.

Article Abstract

In vertebrates, retinal neural circuitry for visual perception is organized in specific layers. The outer plexiform layer is the first synaptic region in the visual pathway, where photoreceptor synaptic terminals connect with bipolar and horizontal cell processes. However, molecular mechanisms underlying cone synapse formation to mediate OFF pathways remain unknown. This study reveals that Necl-1/CADM3 is localized at S- and S/M-opsin-containing cones and dendrites of type 4 OFF cone bipolar cells (CBCs). In mouse retina, synapses between cones and type 4 OFF CBCs were dislocated, horizontal cell distribution became abnormal, and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors were dislocated. mice exhibited aberrant short-wavelength-light-elicited signal transmission from cones to OFF CBCs, which was rescued by AMPA receptor potentiator. Additionally, mice showed impaired optokinetic responses. These findings suggest that Necl-1 regulates cone synapse formation to mediate OFF cone pathways elicited by short-wavelength light in mouse retina.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11016759PMC
http://dx.doi.org/10.1016/j.isci.2024.109577DOI Listing

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