Microglial cells isolated from newborn rat brain displayed a baseline
immunoreactivity for intercellular adhesion molecule-1 (ICAM-1) after
10-20 days in culture. ICAM-1 immunoreactivity was enhanced in a time-
dependent fashion by exposing the microglial cells to recombinant rat
gamma-interferon (gamma-IFN; 100 U/ml) or tumor necrosis factor-alpha
(TNF-alpha; 1000 U/ml). We conclude that rat brain macrophages/microgl
iaI cells can be induced by gamma-IFN and TNF-alpha to express ICAM-1.
This may be relevant in the interaction of microglial cells with othe
r brain cells during inflammation of the central nervous system.