Abstract
Macrophages are critical cells in mediating the pathology of neurodegenerative disorders and enhancement of neuronal outward potassium (K^+^) current has implicated in neuronal apoptosis. To understand how activated macrophages induce neuronal dysfunction and injury, we studied the effects of lipopolysaccharide (LPS)‐stimulated human monocytes‐derived macrophage (MDM) on neuronal outward delayed rectifier K^+^ current (I~K~) and resultant change on neuronal viability in primary rat hippocampal neuronal culture. Bath application of LPS‐stimulated MDM‐conditioned media (MCM) enhanced neuronal I~K~ in a concentration‐dependentmanner, whereas non‐stimulated MCM failed to alter neuronal I~K~. The enhancement of neuronal I~K~ was repeated in a macrophage‐neuronal co‐culture system. The link of stimulated MCM (MCM(+))‐associated enhancement of I~K~ to MCM(+)‐induced neuronal injury, as detected by PI/DAPI (propidium iodide/4′,6‐diamidino‐2‐phenylindol) staining and MTT assay, was demonstrated by experimental results showing that addition of I~K~ blocker tetraethylammonium to the culture protected hippocampal neurons from MCM(+)‐associated challenge. Further investigation revealed elevated levels of K~v~ 1.3 and K~v~ 1.5 channel expression in hippocampal neurons after addition of MCM(+) to the culture. These results suggest that during brain inflammation macrophages, through their capacity of releasing bioactive molecules, induce neuronal injury by enhancing neuronal I~K~ and that modulation of K~v~ channels is a new approach to neuroprotection. © 2009 Wiley‐Liss, Inc.