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. 2024 Feb 1;134(3):e163145. doi: 10.1172/JCI163145

Figure 1. Ezh2 is developmentally downregulated in the nervous system and upregulated in DRG neurons following peripheral nerve injury.

Figure 1

(A and B) Representative immunoblotting showing that Ezh2 is developmentally downregulated in the DRG (A) and cerebral cortex (B). (C) Immunoblotting showing that Ezh2 is significantly increased in L4/5 DRGs 3 days after sciatic nerve transection. (D) Quantification of relative protein levels of Ezh2 in A (n = 2 independent experiments). (E) Quantification of relative protein levels of Ezh2 in B (1-way ANOVA followed by Tukey’s multiple comparisons; P 0.0001; n = 3 independent experiments). (F) Quantification of relative protein levels of Ezh2 in C (unpaired, 2-tailed t test; P = 0.0092; n = 3 for sham, n = 5 for sciatic nerve transection). (G) Representative immunofluorescence of DRG sections showing increased H3K27me3 levels in nuclei of DRG neurons 1 or 3 days after sciatic nerve transection. DRG sections were stained with anti-H3K27me3 (green) and anti-β-tubulin III (red). The rightmost column displays enlarged images of the areas outlined in white, dashed boxes. Yellow arrows indicate H3K27me3 in nuclei of DRG neurons. Scale bars: 100 μm, 30 μm for enlarged images. (H) Quantification of fluorescence intensity of H3K27me3 immunoreactivity in DRG neurons in G (1-way ANOVA followed by Tukey’s multiple comparisons; P 0.0001; n = 3 mice for all). SNT, sciatic nerve transection. **P 0.01, ***P 0.001, ****P 0.0001.