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. 2020 Aug 3;147(21):dev189019. doi: 10.1242/dev.189019

Fig. 3.

Fig. 3.

Increased number of microglial precursors and differentiating microglia in Npc1nmf164 mice at P10. (A) Images of P10 whole cerebellum sections immunostained with IBA1 showing the distribution and abundance of IBA1+ cells in WT and Npc1nmf164 mice. Boxes indicate some regions of WM. (B) High magnification images of the WMR immunostained with IBA1 and KI67 showing higher number of IBA1+ cells in the Npc1nmf164 mouse. AT, axonal tract. (C) High magnified images in a region of the cerebellar cortex immunostained with IBA1 and KI67 showing higher number of IBA1+ cells in the Npc1nmf164 mouse. (D) Quantification of the volume of IBA1+ microglia clusters in the cerebellar WMR. (E) No differences were found in the percentage of WM IBA1+/KI67+ cells between WT and Npc1nmf164 mice. (F) Quantification of the number of IBA1+ cells in the PCL/ML and PS. (G) Quantification of the number of IBA1+/KI67+ cells in the PCL/ML and PS. Data are presented as mean±s.e.m. (D,E) n=2 images per mouse, n=4 mice; (F,G) n=4 mice. *P<0.05. n.s., not significant; u.a., unit area. Scale bars: 250 µm (A); 30 µm (B,C).