Cunnane S C, Keeling P W, Thompson R P, Crawford M A
Br J Nutr. 1984 Mar;51(2):209-17. doi: 10.1079/bjn19840025.
Peripheral blood leucocytes from human male volunteers and from male rats were incubated in vitro in the presence of 14C-labelled linoleic acid [( 14C]LA) or 3H-labelled arachidonic acid [( 3H]AA). The time-course of [14C]LA and [3H]AA incorporation into human leucocyte total lipids was maximal at 80-90% of the initial dose within 20-30 min of dosing the cells. Compared with mixed leucocytes, isolated polymorphonuclear leucocytes were only marginally different in the differential incorporation of [14C]LA and [3H]AA into total lipids. In human leucocytes, [14C]LA was incorporated initially into triglycerides but predominantly into phosphatidylcholine thereafter. In the rat, [14C]LA remained as the free acid (63%), with lesser amounts entering the phospholipids (9%), monoglycerides-diglycerides (12%) and triglycerides (less than 1%). Utilization of [14C]LA by the delta 6-desaturase was only a minor route of its metabolism in both human and rat leucocytes. 3H-labelled prostaglandins E2 and F2 alpha accounted for up to 30% of the radioactivity released into the incubation medium from human leucocytes incubated with [3H]AA for 60 min. Stimulation of phagocytosis in the human leucocytes with latex beads or with unopsonized zymosan did not alter the differential incorporation of [14C]LA or [3H]AA into the leucocyte lipid fractions.