TRAIL is a cell-associated tumor necrosis factor-related apoptosis-inducing
ligand originally identified in immune cells. The ligand has the capacity
to induce apoptosis after binding to cell surface receptors. To examine TRA
IL expression in murine vascular tissue, we employed in situ hybridization
and immunohistochemistry. In these studies, we found that TRAIL mRNA and pr
otein were specifically localized throughout the medial smooth muscle cell
layer of the pulmonary artery. Notably, a similar pattern of expression was
observed in the mouse aorta. Consistent with these findings, we found that
cultures of primary human aorta and pulmonary artery smooth muscle cells e
xpress abundant TRAIL mRNA and protein. We also found that these cells and
endothelial cells undergo cell lysis in response to exogenous addition of T
RAIL. Last, we confirmed that TRAIL specifically activated a death program
by confirming poly(ADP ribose) polymerase cleavage. Overall, we believe tha
t these findings are relevant to understanding the factors that regulate ce
ll turnover in the vessel wall.