A new role for excitation in the retinal direction-selective circuit

Lea Ankri*, Serena Riccitelli, Michal Rivlin-Etzion*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Abstract: A key feature of the receptive field of neurons in the visual system is their centre–surround antagonism, whereby the centre and the surround exhibit responses of opposite polarity. This organization is thought to enhance visual acuity, but whether and how such antagonism plays a role in more complex processing remains poorly understood. Here, we investigate the role of centre and surround receptive fields in retinal direction selectivity by exposing posterior-preferring On–Off direction-selective ganglion cells (pDSGCs) to adaptive light and recording their response to globally moving objects. We reveal that light adaptation leads to surround expansion in pDSGCs. The pDSGCs maintain their original directional tuning in the centre receptive field, but present the oppositely tuned response in their surround. Notably, although inhibition is the main substrate for retinal direction selectivity, we found that following light adaptation, both the centre- and surround-mediated responses originate from directionally tuned excitatory inputs. Multi-electrode array recordings show similar oppositely tuned responses in other DSGC subtypes. Together, these data attribute a new role for excitation in the direction-selective circuit. This excitation carries an antagonistic centre–surround property, possibly designed to sharpen the detection of motion direction in the retina. (Figure presented.). Key points: Receptive fields of direction-selective retinal ganglion cells expand asymmetrically following light adaptation. The increase in the surround receptive field generates a delayed spiking phase that is tuned to the null direction and is mediated by excitation. Following light adaptation, excitation rules the computation in the centre receptive field and is tuned to the preferred direction. GABAergic and glycinergic inputs modulate the null-tuned delayed response differentially. Null-tuned delayed spiking phases can be detected in all types of direction-selective retinal ganglion cells. Light adaptation exposes a hidden directional excitation in the circuit, which is tuned to opposite directions in the centre and surround receptive fields.

Original languageEnglish
Pages (from-to)6301-6328
Number of pages28
JournalJournal of Physiology
Volume602
Issue number22
DOIs
Publication statusPublished Online - 27 Oct 2024

Funding

This work was supported by research grants from the European Research Council (ERC starter no. 757732), the Israeli Centers of Research Excellence (I-CORE; grant no. 51/11), Israel Science Foundation (2449/20) and the Minerva Stiftung with funding from the federal German ministry for education and research. We also acknowledge support from Dr and Mrs Alan Leshner, the Lubin-Schupf Fund for Women in Science, the Charles and David Wolfson Charitable Trust, Rolf Wiklund and Alice Wiklund Parkinson's disease research fund, Consolidated Anti-Aging Foundation, Dr Daniel C. Andreae and Ms Lois Pope. L.A. was supported by the Israel Scholarship Education Foundation (ISEF). S.R. was supported by the Dean of Faculty fellowship. We thank Dr Hillary Voet for her help with the statistics in the manuscript. This work was supported by research grants from the European Research Council (ERC starter no. 757732), the Israeli Centers of Research Excellence (I‐CORE; grant no. 51/11), Israel Science Foundation (2449/20) and the Minerva Stiftung with funding from the federal German ministry for education and research. We also acknowledge support from Dr and Mrs Alan Leshner, the Lubin‐Schupf Fund for Women in Science, the Charles and David Wolfson Charitable Trust, Rolf Wiklund and Alice Wiklund Parkinson's disease research fund, Consolidated Anti‐Aging Foundation, Dr Daniel C. Andreae and Ms Lois Pope. L.A. was supported by the Israel Scholarship Education Foundation (ISEF). S.R. was supported by the Dean of Faculty fellowship.

All Science Journal Classification (ASJC) codes

  • Physiology

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