Proteinase inhibitor–9 expression is induced by maturation in dendritic cells via p38 MAP kinase

SummaryDendritic cells (DC) are crucial for the induction of CD8+ T cell responses. However, as DC present antigen, they may also be at risk for being killed by recent activated CD8+ T cells. Previously we have shown that lipopolysaccharide (LPS)- or CD40L-stimulated monocyte-derived DC express high levels of the granzyme B–inhibitory serpin proteinase inhibitor–9 (PI-9). Furthermore we found that its murine homolog serine protease inhibitor–6 (SPI-6) protected murine DC against cytotoxic T lymphocyte–induced apoptosis. These data suggest that PI-9/SPI-6 may regulate survival of DC when they are under attack by effector cells. We therefore analyzed how PI-9 is regulated upon stimulation with several Toll-like receptor ligands. We found that the expression of PI-9 correlated with maturation, as measured with CD86 levels, but not with the production of interleukin-12–p70. Using LPS as stimulus, we also showed that the induction of PI-9 is dependent on the p38 mitogen-activated protein kinase signaling pathway. The data suggest that PI-9 is tightly linked to maturation and may allow DC to exert their function in a potentially hostile environment.