Arsenical compounds, known to be human carcinogens, were shown to dist
urb cell cycle progression and induce cytogenetic alterations in a var
iety of cell systems. We report here that a 24 h treatment of arsenite
induced mitotic accumulation in human cell lines. HeLa S3 and KB cell
s were most susceptible: 35% of the total cell population was arrested
at the mitotic stage after treatment with 5 mu M sodium arsenite in H
eLa S3 cells and after 10 mu M in KB cells. Under a microscope, we obs
erved abnormal mitotic figures in arsenite-arrested mitotic cells, inc
luding deranged chromosome congression, elongated polar distance of mi
totic spindle, and enhanced microtubule immunofluorescence. The spindl
e microtubules of arsenite-arrested mitotic cells were more resistant
to nocodazole-induced dissolution than those of control mitotic cells.
According to turbidity assay, arsenite at concentrations below 100 mu
M significantly enhanced polymerization of tubulins, Since spindle dy
namics play a crucial role in mitotic progression, our results suggest
that arsenite-induced mitotic arrest may be due to arsenite's effects
on attenuation of spindle dynamics.