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Spatially asymmetric reorganization of inhibition establishes a motion-sensitive circuit

Author

Listed:
  • Keisuke Yonehara

    (Neural Circuit Laboratories, Friedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland)

  • Kamill Balint

    (Neural Circuit Laboratories, Friedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland)

  • Masaharu Noda

    (National Institute for Basic Biology, 444-8787 Okazaki, Japan
    School of Life Science, The Graduate University for Advanced Studies, 444-8787 Okazaki, Japan)

  • Georg Nagel

    (Universität Würzburg, Botanik I, Julius-von-Sachs-Platz 2, 97082 Würzburg, Germany)

  • Ernst Bamberg

    (Max-Planck-Institut für Biophysik, Max-von-Laue Strasse 3, 60438 Frankfurt, Germany
    Johann Wolfgang Goethe-Universität, Institut für Biophysikalische Chemie, Max-von-Laue-Strasse 9, 60438 Frankfurt, Germany)

  • Botond Roska

    (Neural Circuit Laboratories, Friedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland)

Abstract

How the retina gains a sense of direction The ability to detect motion in the visual scene is a fundamental computation in the visual system that is first performed in the retina. The cells responsible for encoding motion direction are the direction-sensitive ganglion cells (DSGCs), which fire a maximum number of action potentials during movement in one direction and fire minimally during movement in the opposite direction. Highly selective wiring from inhibitory cells contributes to determining the direction-selection characteristics of these ganglion cells, yet how the asymmetric wiring inherent to these connections is established was unknown. Two groups using complementary techniques, including pharmacology, electrophysiology and optogenetics, report that although inhibitory inputs to both sides of the direction-selective cell are uniform early in development, by the second postnatal week, inhibitory synapses on the null side strengthen while those on the preferred side remain constant. These plasticity changes occur independent of neural activity, suggesting a specific developmental program is executed to produce the direction-selective circuitry in the retina.

Suggested Citation

  • Keisuke Yonehara & Kamill Balint & Masaharu Noda & Georg Nagel & Ernst Bamberg & Botond Roska, 2011. "Spatially asymmetric reorganization of inhibition establishes a motion-sensitive circuit," Nature, Nature, vol. 469(7330), pages 407-410, January.
  • Handle: RePEc:nat:nature:v:469:y:2011:i:7330:d:10.1038_nature09711
    DOI: 10.1038/nature09711
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    Cited by:

    1. Elishai Ezra-Tsur & Oren Amsalem & Lea Ankri & Pritish Patil & Idan Segev & Michal Rivlin-Etzion, 2021. "Realistic retinal modeling unravels the differential role of excitation and inhibition to starburst amacrine cells in direction selectivity," PLOS Computational Biology, Public Library of Science, vol. 17(12), pages 1-31, December.
    2. Adam Mani & Xinzhu Yang & Tiffany A. Zhao & Megan L. Leyrer & Daniel Schreck & David M. Berson, 2023. "A circuit suppressing retinal drive to the optokinetic system during fast image motion," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    3. Héctor Acarón Ledesma & Jennifer Ding & Swen Oosterboer & Xiaolin Huang & Qiang Chen & Sui Wang & Michael Z. Lin & Wei Wei, 2024. "Dendritic mGluR2 and perisomatic Kv3 signaling regulate dendritic computation of mouse starburst amacrine cells," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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