Microglia, the resident macrophages of the brain, are monocytic cells
whose phenotype is determined during development by the unique environ
ment of the central nervous system (CNS). They are quiescent cells whe
n compared with other tissue macrophages, and this downregulation may
have important consequences for inflammatory and immune responses in t
he brain. In the search for features of the brain environment which mi
ght exert an influence on microglial behaviour, we have concentrated o
n the possible role of adhesion molecules. We have developed a robust
and reproducible in vitro adhesion assay to look at the interaction be
tween macrophages and brain tissue. We describe here the characterisat
ion of this assay. By injecting agents into the brain in vivo, we were
able to study the effect of perturbations in the resident cell popula
tion on the adhesion of macrophages to brain tissue in vitro. This pro
vided strong evidence that RAW 264 cells adhere to neurones in prefere
nce to other CNS cell types in this assay, and this was confirmed by a
dhesion assays performed on monolayers of individual cell types. We hy
pothesise from these results that macrophages interact with CNS neuron
es in vivo via adhesion molecules, enabling them to sense and respond
rapidly to pathology in the brain. (C) 1998 Wiley-Liss, Inc.