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A unique and evolutionarily conserved retinal interneuron relays rod and cone input to the inner plexiform layer

View ORCID ProfileBrent K. Young, Charu Ramakrishnan, Tushar Ganjawala, Yumei Li, Sangbae Kim, Ping Wang, Rui Chen, Karl Deisseroth, Ning Tian
doi: https://doi.org/10.1101/2020.05.16.100008
Brent K. Young
1Ophthalmology and Visual Sciences, University of Utah, UT, 84132, USA.
2Interdepartmental Neuroscience Program, University of Utah, UT, 84114, USA.
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  • ORCID record for Brent K. Young
Charu Ramakrishnan
3Department of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA.
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Tushar Ganjawala
4Department of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, MI 48202, USA.
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Yumei Li
5HGSC, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
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Sangbae Kim
5HGSC, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
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Ping Wang
1Ophthalmology and Visual Sciences, University of Utah, UT, 84132, USA.
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Rui Chen
5HGSC, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
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Karl Deisseroth
3Department of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA.
6Howard Hughes Medical Institute, Stanford, CA 94305, USA.
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Ning Tian
1Ophthalmology and Visual Sciences, University of Utah, UT, 84132, USA.
2Interdepartmental Neuroscience Program, University of Utah, UT, 84114, USA.
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  • For correspondence: ning.tian@hsc.utah.edu
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Abstract

Neurons in the CNS are distinguished from each other by their morphology, the types of the neurotransmitter they release, their synaptic connections, and their genetic profiles. While attempting to characterize the retinal bipolar cell (BC) input to retinal ganglion cells (RGCs), we discovered a previously undescribed type of interneuron in mice and primates. This interneuron shares some morphological, physiological, and molecular features with traditional BCs, such as having dendrites that ramify in the outer plexiform layer (OPL) and axons that ramify in the inner plexiform layer (IPL) to relay visual signals from photoreceptors to inner retinal neurons. It also shares some features with amacrine cells, particularly Aii amacrine cells, such as their axonal morphology and possibly the release of the inhibitory neurotransmitter glycine, along with the expression of some amacrine cell specific markers. Thus, we unveil an unrecognized type of interneuron, which may play unique roles in vision.

Significance Statement Cell types are the building blocks upon which neural circuitry is based. In the retina, it is widely believed that all neuronal types have been identified. We describe a cell type, which we call the Campana cell, that does not fit into the conventional neuronal retina categories but is evolutionarily conserved. Unlike retinal bipolar cells, the Campana cell receives synaptic input from both rods and cones, has broad axonal ramifications, and may release an inhibitory neurotransmitter. Unlike retinal amacrine cells, the Campana cell receives direct photoreceptor input has bipolar-like ribbon synapses. With this discovery, we open the possibility for new forms of visual processing in the retina.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted May 17, 2020.
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A unique and evolutionarily conserved retinal interneuron relays rod and cone input to the inner plexiform layer
Brent K. Young, Charu Ramakrishnan, Tushar Ganjawala, Yumei Li, Sangbae Kim, Ping Wang, Rui Chen, Karl Deisseroth, Ning Tian
bioRxiv 2020.05.16.100008; doi: https://doi.org/10.1101/2020.05.16.100008
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A unique and evolutionarily conserved retinal interneuron relays rod and cone input to the inner plexiform layer
Brent K. Young, Charu Ramakrishnan, Tushar Ganjawala, Yumei Li, Sangbae Kim, Ping Wang, Rui Chen, Karl Deisseroth, Ning Tian
bioRxiv 2020.05.16.100008; doi: https://doi.org/10.1101/2020.05.16.100008

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