Lysophosphatidylcholine induces apoptotic and non-apoptotic death in vascular smooth muscle cells: in comparison with oxidized LDL

Oxidized low-density lipoprotein (oxLDL) plays a key role in the developmen t of atherogenesis, partly by causing injury to vascular cells. However, di fferent preparations of LDL, methods of oxidation, and/or active components often produce cellular effects of various degrees. To explore the quantita tive relationship between dose and level of oxidation of the oxLDL utilized , we employed combinations of different levels of oxidation and concentrati ons of oxLDL to induce cell death in cultured vascular smooth muscle cells (VSMC). We also examined the effect of lysophosphatidylcholine (lysoPC), a putative active component of oxLDL, on VSMCs by determining, in parallel wi th a cytotoxicity test (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliu m bromide (MTT) assay), DNA fragmentation ([H-3]thymidine release), and flo w cytometric analyses. We found that oxLDL caused cytotoxicity in an oxidat ive level- and dose-dependent manner, lysoPC also caused dose-dependent cyt otoxicity with or without serum. Fragmentation of DNA was observed in both oxLDL- and lysoPC-treated VSMCs. Furthermore, lysoPC-induced DNA ladder was also demonstrated by gel electrophoresis at a concentration of 25 mu mol/l or higher. Flow cytometric analysis yielded similar results for oxLDL- and lysoPC-treated VSMC; namely, an accumulation in the fraction of cells in G (0)/G(1) phase with a reciprocal change in S-phase fraction. Membrane phosp hatidylserine exposure, detected by annexin V staining, provided additional evidence that lysoPC induced significant apoptosis in VSMC. Taken together : the degree of oxLDL-induced cytotoxicity/apoptosis of VSMC depended on co mbined effects of oxLDL concentration and oxidative level. Moreover, lysoPC also elicited a dose-dependent apoptosis in addition to cytotoxicity. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.