The cardiac renin-angiotensin system has been suggested to be involved
in various pathological conditions, including hypertrophy and remodel
ing. However, direct evidence that the renin synthesized in situ is re
ally involved in the putative angiotensin II generation is still lacki
ng because of the relatively low abundance of renin mRNA in cardiac ti
ssues. We evaluated renin mRNA expression levels in the ventricles und
er various pathological conditions and found that renin gene expressio
n was markedly increased in the ventricles of isoproterenol-treated ra
ts. Renin mRNA expression levels in the ventricles of rats that had be
en injected with isoproterenol (150 mg/kg SC) were transiently and mar
kedly increased to 6-, 90-, and 4-fold compared with control expressio
n levels at 24, 72, and 120 hours, respectively, after isoproterenol a
dministration. Immunohistochemical analysis revealed that some of the
OX-42-positive macrophage/monocyte cells had a reninlike immunoreactiv
ity. An in vitro experiment indicated that rat peritoneal macrophage/m
onocyte cells expressed renin mRNA in abundance. The present study con
firmed that a subpopulation of macrophage/monocyte cells could express
renin. Macrophage/monocyte cells may be a source of tissue renin in s
ome pathological conditions.