Turnover of phospholipids in rat aortic smooth muscle cells in culture

Smooth muscle cells derived from rat aortic media were explanted and grown in culture for 14 to 60 days. During that time they formed a confluent multilayer and depostied extracellular material resembling newly formed elastin. The lipid composition of the cells in culture differed slightly from the parent cells in the intact aorta with respect to a higher phospholipid/DNA ratio and a higher lecithin content. The cholesterol content resembled that of parent cells. After incubation with labeled precursor the cultured cells show an active lipid synthesis; choline is incorporated mainly into lecithin, whereas glycerol and palmitate appear in phospholipids and to a lesser extent in neutral lipids. After a 2 hour pulse and up to 96 hour chase there is a linear fall in the specific acitivty of lecithin with a half-time of 28 to 30 hours. The rate of fall in specific activity of glycerol- or choline-labeled lecithin was found to be similar, indicating that choline does not turn over by an exchange reaction and is a suitable marker for studying phospholipid turnover in cultured cells. The results provide a basis for investigation of the effect of increasing cellular cholesterol content on phospholipid turnover.