The movements of cultured microglia obtained from newborn rat brain we
re examined by video enhanced-differential interference contrast (VEC-
DIC) microscopy. Active microglia measured 9.03 +/- 1.06 mu m in diame
ter (mean +/- SD, n = 33; range, 7.03-10.36 mu m). The microglia appea
red to become smaller with spread of lamellipodia. The short axis of a
ctively moving microglia measured 7.03 +/- 0.49 mu m (n = 7). The lame
llipodia were thin, transparent and developed rapidly around the cell
body (maximal speed of extension, 4 or 5 mu m/s). When shear stress fr
om the medium was applied to the surface of cultured cells, the microg
lia swam with flat lamellipodia serving as sails in the stream. Sponta
neous non-amoeboid movements of microglia were observed: they pivoted,
circled and marched in various directions using their lamellipodia. T
he angular speed of rotation was maximally 3 degrees/s. In 5 marching
cells, the average speed (distance/s) was calculated at 1.01 +/- 0.54
mu m/s (ca. 60 mu m/min or 3.6 mu m/h).