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. 2020 Apr 25;17:132. doi: 10.1186/s12974-020-01801-9

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 7 — GFP-positive microglia cells and monocytes infiltration of laser CNV spot ex vivo in CX3CR1^gfp/+ mice with L-VGCC blockade. Retinal pigment epithelia choroid-scleral complexes (RCSC) flat mounts indicate infiltration with GPF-positive cells of the laser CNV spot in vehicle-treated control CX3CR1^gfp/+ animals (a) or Zinc20267861 (10 μg) (b) subconjunctivally treated eyes 5 days after model induction. Naive control CX3CR1^gfp/+ mice RCSC flat mounts shows minimal presence of GFP-positive cells (c). Quantitative analysis of GFP-positive cell infiltration area (d). Student t-test was used to determine statistical significance. ***p < 0.001, (n = 3)