J Biol Chem, Vol. 273, Issue 33, 20852-20859, August 14, 1998

Selective Activation of an Apoptotic Retinoid Precursor in Macrophage Cell Lines

Serge V. Yarovoi, Xian-Ping Lu^¶, Nathalie Picard^¶, Deepa Rungta^¶, Darryl Rideout^¶, and Magnus Pfahl^¶

From the  Sidney Kimmel Cancer Center, ^¶ Galderma Research, Inc., and  Maxia Pharmaceuticals, Inc., San Diego, California 92121

Advances in the understanding of the retinoid signaling mechanism has allowed the discovery of highly selective retinoids that activate only one specific receptor class, subtype, or signaling pathway. These novel compounds lack certain of the common retinoid toxicities and therefore suggest promising new approaches for therapeutic applications. We describe here a new compound, 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid methyl ester (MX84), that is selectively activated in macrophages, leading to killing of only macrophage monocyte type cells in vitro. We provide evidence that MX84 is an inactive precursor that is converted into an active apoptosis-inducing retinoid in macrophages. The macrophage activity is also secreted, and our data suggest that the secreted activity is a phospholipase D type activity. Our observation may lead to the development of molecules that are highly macrophage-selective apoptosis inducers in vivo and that could represent important novel therapeutics against diseases caused by excessive macrophage activity.