Interleukin-8 (IL-8) is a chemokine produced by a variety of cell type
s involved in atherogenesis and is chemotactic for neutrophils and lym
phocytes. A recent study has shown that IL-8 is angiogenic and induces
proliferation and chemotaxis of endothelial cells. The present study
was undertaken to find out whether IL-8 is also mitogenic and chemotac
tic for vascular smooth muscle cells. IL-8 induced a concentration-dep
endent (0.1 to 10 nmol/L) stimulation of DNA synthesis and cell prolif
eration in both human and rat aortic smooth muscle cells. In addition,
IL-8 stimulated smooth muscle cells to produce prostaglandin E(2), wh
ich can inhibit IL-8-induced smooth muscle cell proliferation. In the
presence of indomethacin (5 mu mol/L), IL-8 (1 nmol/L) stimulated an i
ncrease in human and rat aortic smooth muscle cell number during a 3-d
ay period of incubation by 61+/-16% and 59+/-7% (n=4), respectively. I
L-8 also increased DNA synthesis in human and rat aortic smooth muscle
cells by 98+/-10% and 151+/-27% (n=5), respectively. Moreover, IL-8 s
timulated rat aortic smooth muscle cell migration by 20-fold over the
control value, with an EC(50) value of 0.83 nmol/L; this chemotactic a
ctivity of IL-8 was also potentiated by indomethacin. Exposure of smoo
th muscle cells to IL-8 caused rapid and transient expression of the i
mmediate-early genes c-fos and zif268 mRNA. The maximal levels of c-fo
s and zif268 mRNA in human and rat aortic smooth muscle cells were obs
erved 30 minutes and 1 hour after stimulation with IL-8, respectively,
followed by rapid decline. Moreover, IL-8 stimulated mitogen activate
d protein (MAP) kinase in smooth muscle eels with a peak at 5 to 10 mi
nutes after stimulation. At 1 and 10 nmol/L IL-8, MAP kinase activity
increased by 1.5- and 7-fold above the basal level, respectively. Sinc
e vascular smooth muscle cell proliferation and migration are crucial
steps in neointimal formation in restenosis and atherosclerosis, these
results suggest that IL-8 may be an important naturally occurring mit
ogen and chemoattractant for vascular smooth muscle cells and may play
a role in the pathogenesis of arterial intimal thickening and atheros
clerosis.