Retinal Ganglion Cells Can Rapidly Change Polarity from Off to On
Abstract
Retinal ganglion cells are commonly classified as On-center or Off-center depending on whether they are excited predominantly by brightening or dimming within the receptive field. Here we report that many ganglion cells in the salamander retina can switch from one response type to the other, depending on stimulus events far from the receptive field. Specifically, a shift of the peripheral image—as produced by a rapid eye movement—causes a brief transition in visual sensitivity from Off-type to On-type for approximately 100 ms. We show that these ganglion cells receive inputs from both On and Off bipolar cells, and the Off inputs are normally dominant. The peripheral shift strongly modulates the strength of these two inputs in opposite directions, facilitating the On pathway and suppressing the Off pathway. Furthermore, we identify certain wide-field amacrine cells that contribute to this modulation. Depolarizing such an amacrine cell affects nearby ganglion cells in the same way as the peripheral image shift, facilitating the On inputs and suppressing the Off inputs. This study illustrates how inhibitory interneurons can rapidly gate the flow of information within a circuit, dramatically altering the behavior of the principal neurons in the course of a computation.
Additional Information
© 2007 Geffen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Received June 20, 2006; Accepted December 28, 2006; Published March 6, 2007. We are grateful for many discussions with Haim Sompolinsky, Daniel Fisher, Stephen Baccus, Bence Ölveczky, and members of the Meister laboratory. Author Contributions: MNG, SEJdV, and MM conceived and designed the experiments. MNG and SEJdV performed the experiments. MNG, SEJdV, and MM analyzed the data. MNG and MM wrote the paper. The work was supported by predoctoral fellowships from the Howard Hughes Medical Institute (MNG) and the National Science Foundation (SEJDV), and grants EY10020 and EY14737 from the National Eye Institute (MM). The authors have declared that no competing interests exist.Attached Files
Published - journal.pbio.0050065.PDF
Erratum - journal.pbio.0050136.pdf
Erratum - journal.pbio.0050188.pdf
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Additional details
- PMCID
- PMC1808116
- Eprint ID
- 75724
- Resolver ID
- CaltechAUTHORS:20170405-082620129
- Howard Hughes Medical Institute (HHMI)
- NSF
- NIH
- EY10020
- NIH
- EY14737
- National Eye Institute
- Created
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2017-04-05Created from EPrint's datestamp field
- Updated
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2023-06-01Created from EPrint's last_modified field