Role of acidic Ca2+-independent phospholipase A2 in synthesis of lung dipalmitoyl phosphatidylcholine

Am J Physiol. 1997 Feb;272(2 Pt 1):L238-43. doi: 10.1152/ajplung.1997.272.2.L238.

Abstract

Dipalmitoyl phosphatidylcholine (deltaPC) synthesis by lung epithelium occurs in part by a deacylation/reacylation pathway utilizing phospholipase A2 (PLA2) and an acyl transferase. The role of acidic Ca2+-independent PLA2 (aiPLA2) in this pathway was investigated using a transition-state analog enzyme inhibitor [1-hexadecyl-3-trifluoroethylglycero-sn-2-phosphomethanol (MJ33)]. Granular pneumocytes were isolated from rat lung with elastase and were maintained in primary culture for 24 h on microporous membranes in the presence of radiolabeled choline or free fatty acids (palmitate plus oleate). Disaturated phosphatidylcholine (DSPC) was determined by osmication chromatography. Incorporation (nmol/mg protein) into DSPC at 24 h incubation was 11.9 +/- 0.2 for [3H]choline and 12.1 +/- 0.04 for [3H]palmitate. In the presence of 3 mol% MJ33, incorporation of [3H] choline and [3H]palmitate was decreased by 37 and 69%, respectively, and DSPC pool size (microg/mg cell protein) decreased by 9% (P < 0.05). A similar decrease in radiolabel incorporation was observed with 2 h of incubation. The presence of p-bromophenacyl bromide (20 microm) had a significantly smaller effect that was additive with that of MJ33. After 24 h of labeling and 4 h of chase with unlabeled substrate, there was a significant decrease of radiolabel in DSPC that was inhibited by MJ33. Under all experimental conditions, MJ33 resulted in either no change or a modest increase of radiolabel in the cellular unsaturated PC fraction. These results indicate that aiPLA2 has a major role in DSPC synthesis by granular pneumocytes.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 1,2-Dipalmitoylphosphatidylcholine / biosynthesis*
  • Acids / metabolism*
  • Animals
  • Calcium / physiology*
  • Enzyme Inhibitors / pharmacology
  • Fatty Acids / pharmacology
  • Glycerophosphates / pharmacology
  • Lung / cytology
  • Lung / drug effects
  • Lung / metabolism*
  • Male
  • Methylamines / pharmacology
  • Phospholipases A / antagonists & inhibitors
  • Phospholipases A / physiology*
  • Phospholipases A2
  • Rats
  • Rats, Sprague-Dawley
  • Substrate Specificity

Substances

  • Acids
  • Enzyme Inhibitors
  • Fatty Acids
  • Glycerophosphates
  • Methylamines
  • 1-hexadecyl-3-trifluoroethylglycero-sn-2-phosphomethanol
  • 1,2-Dipalmitoylphosphatidylcholine
  • methylamine
  • Phospholipases A
  • Phospholipases A2
  • Calcium