TY - JOUR
T1 - Inhomogeneous Encoding of the Visual Field in the Mouse Retina
AU - Warwick, Rebekah A
AU - Kaushansky, Nathali
AU - Sarid, Nimrod
AU - Golan, Amir
AU - Rivlin-Etzion, Michal
N1 - We thank Prof. Tali Kimchi (Weizmann Institute of Science) for the supply of wild house mice and Dr. Roy Harpaz and Dr. Ariel Goldstein for statistical advice. We thank Prof. Michal Schwartz, Prof. Ilan Lampl, Prof. Tali Kimchi, and the Rivlin lab for reading and commenting on the manuscript. This project has received funding from the I-CORE (51/11), the Minerva Foundation, the ISF Foundation (1396/15), the European Research Council under the European Union’s Horizon 2020 research and innovation program (grant agreement no. 757732), Dr. and Mrs. Alan Leshner, the Lubin-Schupf Fund for Women in Science, the Charles and David Wolfson Charitable Trust, and Ms. Lois Pope. R.A.W. was supported by the Dean of Faculty fellowship at Weizmann Institute of Science. M.R.-E. is incumbent of the Sara Lee Schupf Family Chair. Author Contributions R.A.W. designed and conducted experiments, analyzed and interpreted the results, and wrote the paper. N.S. assisted with cell fill experiments. A.G. designed the UV stimulus path. N.K. maintained the mouse colonies and performed genotyping. M.R.-E. designed the experiments, interpreted the results, and wrote the paper.
PY - 2018/3/5
Y1 - 2018/3/5
N2 - Stimulus characteristics of the mouse's visual field differ above and below the skyline. Here, we show for the first time that retinal ganglion cells (RGCs), the output neurons of the retina, gradually change their functional properties along the ventral-dorsal axis to allow better representation of the different stimulus characteristics. We conducted two-photon targeted recordings of transient-Offα-RGCs and found that they gradually became more sustained along the ventral-dorsal axis, revealing >5-fold-longer duration responses in the dorsal retina. Using voltage-clamp recordings, pharmacology, and genetic manipulation, we demonstrated that the primary rod pathway underlies this variance. Our findings challenge the current belief that RGCs of the same subtype exhibit the same light responses, regardless of retinal location, and suggest that networks underlying RGC responses may change with retinal location to enable optimized sampling of the visual image. Warwick et al. show that retinal ganglion cells of the same subtype display different light responses depending on retinal location, resulting from variations in their underlying circuits. They suggest that these variations enable optimized sampling of the visual image.
AB - Stimulus characteristics of the mouse's visual field differ above and below the skyline. Here, we show for the first time that retinal ganglion cells (RGCs), the output neurons of the retina, gradually change their functional properties along the ventral-dorsal axis to allow better representation of the different stimulus characteristics. We conducted two-photon targeted recordings of transient-Offα-RGCs and found that they gradually became more sustained along the ventral-dorsal axis, revealing >5-fold-longer duration responses in the dorsal retina. Using voltage-clamp recordings, pharmacology, and genetic manipulation, we demonstrated that the primary rod pathway underlies this variance. Our findings challenge the current belief that RGCs of the same subtype exhibit the same light responses, regardless of retinal location, and suggest that networks underlying RGC responses may change with retinal location to enable optimized sampling of the visual image. Warwick et al. show that retinal ganglion cells of the same subtype display different light responses depending on retinal location, resulting from variations in their underlying circuits. They suggest that these variations enable optimized sampling of the visual image.
UR - http://www.scopus.com/inward/record.url?scp=85042042108&partnerID=8YFLogxK
U2 - 10.1016/j.cub.2018.01.016
DO - 10.1016/j.cub.2018.01.016
M3 - مقالة
C2 - 29456141
SN - 0960-9822
VL - 28
SP - 655
EP - 665
JO - Current biology : CB
JF - Current biology : CB
IS - 5
ER -