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Journal of Neuroscience, Vol 8, 4707-4717, Copyright © 1988 by Society for Neuroscience
Colony-stimulating factors as promoters of ameboid microglia
D Giulian and JE Ingeman
Department of Neurology, Baylor College of Medicine, Houston, Texas 77030.
Immunomodulators were tested for their ability to stimulate proliferation
and biologic activity of ameboid microglia. Only the colony-stimulating
factors (CSFs), multipotential-CSF (multi-CSF) and
granulocyte/macrophage-CSF (GM-CSF), were potent mitogens for microglia.
Other immunomodulators, including interleukin-1, interleukin- 2, interferon
gamma, tumor necrosis factor, or granulocyte-CSF (G-CSF), had no effect
upon microglial growth in vitro. Multi-CSF or GM-CSF were also observed to
induce more rapid phagocytosis of polystyrene microspheres by cultured
ameboid cells. In order to determine which immunomodulators alter brain
inflammatory responses in vivo, we infused recombinant forms of GM-CSF,
multi-CSF, macrophage-CSF, or G-CSF into the cerebral cortex of rats.
Within 48 hr after infusion multi-CSF or GM-CSF stimulated the appearance
of large numbers of mononuclear phagocytes at the site of injection. These
same factors also accelerated the clearance of polystyrene microspheres
from the brain. Our observations indicate that certain classes of
immunomodulators which are mitogens and activators of ameboid microglia in
vitro amplify the inflammatory response of the CNS in vivo by action upon
intrinsic brain mononuclear phagocytes.
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