Active labeling of phosphatidylcholines by [1- 14C]docosahexaenoate in isolated photoreceptor membranes

Abstract

Isolated bovine rod outer segments and photoreceptor disks actively incorporated [1- 14C]docosahexaenoate (22:6) into phospholipids when incubated in the presence of CoA, ATP, and Mg 2+. About 80% of the esterified fatty acid was in phosphatidylcholine (PC). Microsomal and mitochondrial fractions incorporated as much 22:6 as rod outer segments, but it was distributed among various phospholipids and neutral glycerides. The isolated photoreceptor membrane thus contains an acyl-CoA synthetase which activates the fatty acid and a docosahexaenoyl-CoA-lysophosphatidylcholine acyltransferase activity. The specific radioactivity of PC was higher in rod outer segments than in the other subcellular fractions. About 2 3 of the label in photoreceptor membrane PC was in its dipolyunsaturated molecular species and 1 3 in hexaenes. Dipolyunsaturated PCs showed high turnover rates of 22:6 in all three subcellular membranes, especially in mitochondria. Retinal membranes in vitro seem to take up free [ 14C]22:6 from the medium by simple diffusion or partition into the membrane lipid. The ability of these membranes to activate and esterify [1- 14C]22:6 indicates that docosahexaenoate-containing molecular species of retina lipids, including those of photoreceptor membranes, are subject to acylation-deacylation reactions in situ.