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Synthesis of the dipalmitoyl species of diacyl glycerophosphocholine by rabbit alveolar macrophages

Journal Article · · Lipids; (United States)
DOI:https://doi.org/10.1007/BF02534438· OSTI ID:5811200
The distribution of radioactivity among the molecular species of diacyl glycerophosphocholine of rabbit alveolar macrophages was determined after incubation with (/sup 3/H)glycerol and 1-(/sup 14/C)palmitoyl-sn-glycero-3-phosphocholine. The highest percentage of radioactivity of (/sup 3/H)glycerol was found in the dipalmitoyl species (35% of the total) followed by the 1-palmitoyl-2-linoleoyl (23.6%) and 1-stearoyl-2-linoleoyl plus 1-palmitoyl-2-oleoyl species (19.7%) during the first 30 min incubation. The radioactivity of the dipalmitoyl species reached a maximum at 120 min incubation and decreased thereafter, although the radioactivities of other molecular species still increased. In contrast to the (/sup 3/H)glycerol labeling, only 4% of the total radioactivity in diacyl glycerophosphocholine derived from 1-(/sup 14/C)palmitoyl glycerophosphocholine was found in the dipalmitoyl species; 80% of the radioactivity was located in the 1-palmitoyl-2-arachidonoyl species at 10 min incubation. The present results indicate that the dipalmitoyl species of diacyl glycerophosphocholine are synthesized predominantly via a de novo pathway and not the deacylation-reacylation pathway in rabbit alveolar macrophages.
Research Organization:
Teikyo Univ., Kanagawa, Japan
OSTI ID:
5811200
Journal Information:
Lipids; (United States), Journal Name: Lipids; (United States) Vol. 2; ISSN LPDSA
Country of Publication:
United States
Language:
English