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A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks
Cell type-specific Cre driver lines have revolutionized the analysis of retinal cell types and circuits. We show that the transgenic mouse Rbp4-Cre selectively labels several retinal neuronal types relevant to the encoding of absolute light intensity (irradiance) and visual motion. In the ganglion c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411164/ https://www.ncbi.nlm.nih.gov/pubmed/28466070 http://dx.doi.org/10.1523/ENEURO.0065-17.2017 |
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author | Sabbah, Shai Berg, Daniel Papendorp, Carin Briggman, Kevin L. Berson, David M. |
author_facet | Sabbah, Shai Berg, Daniel Papendorp, Carin Briggman, Kevin L. Berson, David M. |
author_sort | Sabbah, Shai |
collection | PubMed |
description | Cell type-specific Cre driver lines have revolutionized the analysis of retinal cell types and circuits. We show that the transgenic mouse Rbp4-Cre selectively labels several retinal neuronal types relevant to the encoding of absolute light intensity (irradiance) and visual motion. In the ganglion cell layer (GCL), most marked cells are wide-field spiking polyaxonal amacrine cells (ACs) with sustained irradiance-encoding ON responses that persist during chemical synaptic blockade. Their arbors spread about 1 mm across the retina and are restricted to the inner half of the ON sublamina of the inner plexiform layer (IPL). There, they costratify with dendrites of M2 intrinsically photosensitive retinal ganglion cells (ipRGCs), to which they are tracer coupled. We propose that synaptically driven and intrinsic photocurrents of M2 cells pass through gap junctions to drive AC light responses. Also marked in this mouse are two types of RGCs. R-cells have a bistratified dendritic arbor, weak directional tuning, and irradiance-encoding ON responses. However, they also receive excitatory OFF input, revealed during ON-channel blockade. Serial blockface electron microscopic (SBEM) reconstruction confirms OFF bipolar input, and reveals that some OFF input derives from a novel type of OFF bipolar cell (BC). R-cells innervate specific layers of the dorsal lateral geniculate nucleus (dLGN) and superior colliculus (SC). The other marked RGC type (RDS) is bistratified, transient, and ON-OFF direction selective (DS). It apparently innervates the nucleus of the optic tract (NOT). The Rbp4-Cre mouse will be valuable for targeting these cell types for further study and for selectively manipulating them for circuit analysis. |
format | Online Article Text |
id | pubmed-5411164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-54111642017-05-02 A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks Sabbah, Shai Berg, Daniel Papendorp, Carin Briggman, Kevin L. Berson, David M. eNeuro New Research Cell type-specific Cre driver lines have revolutionized the analysis of retinal cell types and circuits. We show that the transgenic mouse Rbp4-Cre selectively labels several retinal neuronal types relevant to the encoding of absolute light intensity (irradiance) and visual motion. In the ganglion cell layer (GCL), most marked cells are wide-field spiking polyaxonal amacrine cells (ACs) with sustained irradiance-encoding ON responses that persist during chemical synaptic blockade. Their arbors spread about 1 mm across the retina and are restricted to the inner half of the ON sublamina of the inner plexiform layer (IPL). There, they costratify with dendrites of M2 intrinsically photosensitive retinal ganglion cells (ipRGCs), to which they are tracer coupled. We propose that synaptically driven and intrinsic photocurrents of M2 cells pass through gap junctions to drive AC light responses. Also marked in this mouse are two types of RGCs. R-cells have a bistratified dendritic arbor, weak directional tuning, and irradiance-encoding ON responses. However, they also receive excitatory OFF input, revealed during ON-channel blockade. Serial blockface electron microscopic (SBEM) reconstruction confirms OFF bipolar input, and reveals that some OFF input derives from a novel type of OFF bipolar cell (BC). R-cells innervate specific layers of the dorsal lateral geniculate nucleus (dLGN) and superior colliculus (SC). The other marked RGC type (RDS) is bistratified, transient, and ON-OFF direction selective (DS). It apparently innervates the nucleus of the optic tract (NOT). The Rbp4-Cre mouse will be valuable for targeting these cell types for further study and for selectively manipulating them for circuit analysis. Society for Neuroscience 2017-05-01 /pmc/articles/PMC5411164/ /pubmed/28466070 http://dx.doi.org/10.1523/ENEURO.0065-17.2017 Text en Copyright © 2017 Sabbah et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research Sabbah, Shai Berg, Daniel Papendorp, Carin Briggman, Kevin L. Berson, David M. A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks |
title | A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks |
title_full | A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks |
title_fullStr | A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks |
title_full_unstemmed | A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks |
title_short | A Cre Mouse Line for Probing Irradiance- and Direction-Encoding Retinal Networks |
title_sort | cre mouse line for probing irradiance- and direction-encoding retinal networks |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411164/ https://www.ncbi.nlm.nih.gov/pubmed/28466070 http://dx.doi.org/10.1523/ENEURO.0065-17.2017 |
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