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. 2016 Sep 26;22:1137–1155.

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Copyright © 2016 Molecular Vision.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited, used for non-commercial purposes, and is not altered or transformed.

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Citrullination of GFAP filaments after injury. Cryosections from uninjured and injured eyes were stained with GFAP (red) and F95 (green) and nuclei stained with DAPI (blue). Sections were examined under confocal microscope at 20X magnification in an uninjured state (A-C) and at 1 h (D-F), 3 h (G-I), 1 day (J-L) and 3 days (M-O) postinjury. Extensions of GFAP staining beyond nuclei of the GCL are marked by an arrow (F). Co-localization of GFAP and F95 antibodies are marked by asterisks (F, I, L, O). Interspersed regions of GFAP and F95 reactivity is outlined in brackets (I, O). GFAP-negative, F95-positive filaments are marked by arrowhead (I). GCL, ganglion cell layer; IPL, inner plexiform layer; INL, inner nuclear layer; OPL, outer plexiform layer; ONL, outer nuclear layer. (Scale bar = 100 μm).