This study evaluates using a polymerase chain reaction (PCR)-based mol
ecular biological approach to study the gene expression of the constit
utive endothelial isoform of nitric oxide synthase (ecNOS) in human mo
nocytes. When PCR was carried out with specific primers for ecNOS, 302
bp product was amplified, which sequence analysis determined as havin
g 100% identity to the reported human ecNOS isoform gene sequence. The
data presented here demonstrate a reliable technique for assessing ec
NOS mRNA levels in circulating human monocytes. This then permits use
of this easily available cell to monitor ecNOS levels and provides a m
eans to investigate mechanisms involved in controlling NO synthase lev
els as well as NO synthesis.