Fig. 3From: M2 microglia-derived exosome-loaded electroconductive hydrogel for enhancing neurological recovery after spinal cord injuryAxon outgrowth of NSCs and DRGs in vitro on various materials. (A) Confocal microscopy images showing the expression of neurofilament (NF, red) and β3-tubulin (Tuj-1, Green) in NSCs after 7 days of culture on different samples. Nuclei were stained with Hoechst (blue). Scale bar = 100 μm. (B) Quantification of axon density and axon length in NSCs grown on various materials (n = 3). (C) Gene expression profiles of NSCs cultured on different samples for 7 days (n = 3). (D) Immunofluorescence (IF) images of NF-positive axons in DRGs grown on different samples for 7 days. Scale bar = 200 μm. (E) Quantitative analysis of axon density and length in DRGs (n = 3). (F) Expression of GAP43 and NF proteins in NSCs cultured on different samples for 7 days. (G) Quantification of Western blot data (n = 3). Statistical analysis was performed using ANOVA followed by Tukey’s test (*p < 0.05, **p < 0.01, and ***p < 0.001)Back to article page