Fig. 2From: Lack of a protective effect of the Tmem106b “protective SNP” in the Grn knockout mouse model for frontotemporal lobar degenerationA Representative images of immunofluorescence stainings of the cerebral cortex, thalamus, and the hippocampus (CA3 subfield) of a wildtype, Grn−/−, and Grn−/− × Tmem106bT186S/T186S with an antibody against CD68 (green). B The quantification of the CD68-positive area/section is indicated (n = 5; Age: 6 months). C Representative images of immunofluorescence stainings of the thalamus of a wildtype, Grn−/−, and Grn−/− × Tmem106bT186S/T186S with an antibody against Iba1 (red). Age: 6 month. D Three-dimensional reconstructions from representative microglia cells of a wildtype, Grn−/−, and Grn−/− × T186S/T186S mouse stained for Iba1 (red) and CD68 (green) from 50 images in the Z-direction of the thalamus (age: 6 months). E Volumetric quantification of the microglia cell volume of individual cells depicted from 3D reconstructed images. F Volumetric quantification of the CD68-positive phagosome compartment in individual Iba1-positive microglia cells depicted from 3D reconstructed images. B, E, F *p < 0.05; **p < 0.01; ****p < 0.001; ns Not significantBack to article page