Histology of NDI1-treated retinas following rotenone insult. Adult wild-type mice were intravitreally injected into contralateral eyes with 3 × 109 vp AAV-NDI1 (a, c) and 1 × 108 vp AAV-EGFP (EGFP signals not shown), to facilitate localisation of transduced regions of the retinas, or 3 × 109 vp AAV-EGFP (b, d) alone (n=4). Three weeks post-injection, 1.5 nmol of rotenone was administered intravitreally to both eyes. Three weeks post-rotenone treatment eyes were enucleated, fixed, cryosectioned (12 μm) and processed for immunocytochemistry using NeuN primary and Cy3-conjugated secondary antibodies (red). Nuclei were counterstained with DAPI (blue). (a, b) Overview of retinal histology with or without NDI1 treatment, respectively (light microscopy). (c, d) Detailed view of the ganglion cell (GCL) and inner plexiform (IPL) layers (laser confocal microscopy). Rectangles in a and b demark the areas shown in greater detail in c and d, respectively. ONL, outer nuclear layer; OS, photoreceptor outer segments. Scale bar: 20 μm. (e) Bar chart representing mean ganglion cell counts per 100 μm. Blue and white columns represent values corresponding to AAV-NDI1+rotenone (NDI1) and AAV-EGFP+rotenone (EGFP), respectively. Error bars represent SD values and ***P<0.001.