Evidence for lipid synthesis by the dihydroxyacetone phosphate pathway in rabbit lung subcellular fractions.

Abstract

Lipid synthesis by the lung requires a 3-carbon skeleton that can be provided by sn-glycerol-3-phosphate derived from glycolysis. This study investigated whether acylation of dihydroxyacetone-phosphate can serve as an alternate pathway for lung lipid synthesis. Rabbit lung microsomal and mitochondrial fractions were incubated with radiolabelled sn-glycerol-3-P and/or dihydroxyacetone-P. Palmitoyl CoA was used as acyl donor. The lipid fraction was subsequently isolated and radioactive incorporation was determined. Glycerol-3-P and dihydroxyacetone-P were both incorporated into the lipid fraction when each substrate was present alone. During incubation in the presence of equimolar concentrations of both substrates dihydroxyacetone-P accounted for 41 per cent of the total incorporation. These results show that acylation of dihydroxyacetone phosphate is a potential alternate to the glycerol-3-phosphate pathway for lung lipid synthesis.