Microglia are immunocompetent cells in the brain that have many simila
rities with macrophages of peripheral tissues. In normal adult brain,
microglial cells are in a resting state, but they become activated dur
ing inflammation of the central nervous system, after neuronal injury,
and in several neurological diseases. Patch-clamp studies of microgli
al cells in cell culture and in tissue slices demonstrate that microgl
ia express a wide variety of ion channels. Six different types of K+ c
hannels have been identified in microglia, namely, inward rectifier, d
elayed rectifier, HERG-like, G protein-activated, as well as voltage-d
ependent and voltage-independent Ca2+-activated K+ channels. Moreover,
microglia express H+ channels, Na+ channels, voltage-gated Ca2+ chann
els, Ca2+-release activated Ca2+ channels, and voltage-dependent and v
oltage-independent Cl- channels. With respect to their kinetic and pha
rmacological properties, most microglial ion channels closely resemble
ion channels characterized in other macrophage preparations. Expressi
on patterns of ion channels in microglia depend on the functional stat
e of the cells. Microglial ion channels can be modulated by exposure t
o lipopolysaccharide or various cytokines, by activation of protein ki
nase C or G proteins, by factors released from astrocytes, by changes
in the concentration of internal free Ca2+, and by variations of the i
nternal or external pH. There is evidence suggesting that ion channels
in microglia are involved in maintaining the membrane potential and a
re also involved in proliferation, ramification, and the respiratory b
urst. Further possible functional roles of microglial ion channels are
discussed.