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The structure-activity relationship of various YO compounds, novel plasmin inhibitors, in the apoptosis induction
Riyo Enomoto1, Chiyoko Sugahara, Tomoe Komai
1Department of Pharmacology, Kobe Gakuin University, Ikawadani-cho, Nishi, Kobe 651-2180, Japan.
Abstract:
We have previously reported that YO-2, a selective plasmin inhibitor, induces thymocyte apoptosis. To elucidate the mechanism of YO-2-induced apoptosis, other YO compounds with different plasmin inhibitory action were tested for the pro-apoptotic activity in this study. The treatment of rat thymocytes with the YO compounds which had the hydrophobic but not the hydrophilic moiety at the C-terminal increased DNA fragmentation, the number of condensed nuclei and caspase-3-like activity. All pro-apoptotic YO compounds not only were potent plasmin inhibitors but also had the hydrophobic C-terminal as the common structure. Therefore, the target molecule of the YO compounds may be located not on the cell surface but rather inside the cells.
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