Recent observations have shown that both Chlamydia pneumoniae antigens
and DNA may be found within atherosclerotic lesions. In this study, w
e evaluated the ability of C. pneumoniae to infect cells that make up
atherosclerotic lesions, including endothelial cells, smooth muscle ce
lls, and cholesterol loaded smooth muscle cells. The organism readily
infected rabbit, bovine, and human aortic smooth muscle cells, Cholest
erol-loaded smooth muscle cells were even more susceptible to C. pneum
oniae infection, Chlamydia trachomatis inefficiently infected smooth m
uscle cells, demonstrating that this is not a characteristic of all me
mbers of the genus Chlamydia, C. pneumoniae infected bovine endothelia
l cells poorly. This study demonstrates that C. pneumoniae readily inf
ects one of the important types of cells found within atherosclerotic
lesions, i.e., smooth muscle cells with and without cholesterol loadin
g.