1M and O). Double immunofluorescence showed that cell aggregates in the aged brain are microglia as CD11b positive aggregates were not associated with blood vessels and mainly found in the parenchyma, and are therefore not components of the perivascular macrophage population (Fig. 2A and B). Some aggregates extended processes that made contact with vasculature, but most did not. We also show that these aggregates were not groups of proliferating cells by double staining for CD11c and Ki67 (Fig. 2C). Expression

of CD11c, FcγRI and F4/80 was very weak or not detectable in the 4 month old brain (Fig. 2G–I), but all three markers were robustly expressed in aged cerebellar white matter (Fig. 2D–F). In summary, age dependent changes in morphology and phenotype appear to arise

in a region dependent learn more selleckchem manner, with a specific white matter phenotype present in the aged brain, in particular in the cerebellum. We quantified the expression levels of functional markers in the different regions studied. In the ageing brain an increased expression of CD11b, CD68 and F4/80 (Fig. 3, n = 5 per group): for all three markers there was a strong effect of age on expression level (CD11b: F(1,111) = 38.35, p < 0.001; CD68: F(1,108) = 271.36, p < 0.001; F4/80: F(1,109) = 75.86, p < 0.001). None of these markers were significantly affected by systemic LPS 24 h after injection. Region had a strong effect on expression of all three markers, (CD11b: F(7,111) = 2.45, p = 0.022; CD68: F(7,108) = 7.90, p < 0.001; F4/80: F(7,109) = 4.64, p < 0.001). We detected an interaction between age and region for expression of all three markers (CD11b: F(7,111) = 2.12, p = 0.047; CD68: F(7,108) = 7.789, p < 0.001; F4/80: F(7,109) = 4.64, p < 0.001), suggesting that microglial activation is differentially affected by age in different brain regions. The increases in expression of CD11b, CD68 and F4/80 were greatest in the cerebellum and in particular in the cerebellar inferior peduncles. Microglial expression of all

three markers in the fimbria and for CD11b and CD68 the corpus callosum was also strongly Florfenicol increased in aged animals ( Fig. 3A and B). Changes in the expression of these molecules in the white matter were greater than those in the grey matter. The dentate gyrus did not exhibit any changes in expression with ageing for any of these three markers. The expression levels of CD11c (Fig. 4A) and FcγRI (Fig. 4B) were also quantified and expression of both was significantly increased by age (CD11c: F(1,128) = 63.08, p < 0.001; FcγRI: F(1,92) = 61.37, p < 0.001), region (CD11c: F(7,128) = 15.76, p < 0.001; FcγRI: F(6,92) = 4.84, p < 0.001) and, for FcγRI, LPS injection (F(1,92) = 5.97, p < 0.05). An interaction between age and region was detected for CD11c expression (F(7,128) = 11.72, p < 0.001), but not FcγRI.