Smooth muscle cultures can calcify under certain circumstances. As a model
system these cultures therefore provide information on why calcification oc
curs in atherosclerotic plaques. Whether all smooth muscle cells (under cer
tain conditions), or only specific populations, can produce this mineraliza
tion has not been resolved. Demer's group has cloned calcifying vascular ce
lls from subcultured bovine aorta and studied them in detail. They have spe
culated on whether the cells are smooth muscle which have altered in phenot
ype, or whether they are derived from a stem cell population within the art
ery wall.
The article argues that while the normal process of smooth muscle phenotypi
c modulation seen in arterial repair could account for the observations, th
is view may be two simplistic considering the complex nature of the artery
wall. Certainly there is evidence for heterogeneity of smooth muscle cells
in the artery wall and recent evidence suggests that stem cells can circula
te in the blood and repopulate tissues. Further studies are required to res
olve the important question as to the origin of cells which produce mineral
ization in atheroma.