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. 2017 Oct 31;8:1220. doi: 10.1038/s41467-017-01332-7

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 8 — Spatiotemporal receptive fields of ONα-RGCs and OFFα-RGCs in wild-type and Pcp2-DTA mice. a Representative spatiotemporal receptive field maps from ONα-RGCs (top row) and OFFα-RGCs (bottom row) in wild-type and Pcp2-DTA mice. Because the area of each ring in our circular white noise stimuli was kept constant, rows in the receptive field maps decrease in height with increasing distance from the center. b, c Summary data (mean ± SEM) of the spatial and temporal response profiles at the temporal and spatial absolute response maxima, respectively (WT ONα-RGC n = 12 cells, WT OFFα-RGCs n = 9, n = 4 mice; Pcp2-DTA ONα-RGC n = 6, Pcp2-DTA OFFα-RGC n = 7, n = 3 mice)