Pc. Choy et al., ACYL-GPC AND ALKENYL ALKYL-GPC-ACYL-COA ACYLTRANSFERASES/, Biochimica et biophysica acta, L. Lipids and lipid metabolism, 1348(1-2), 1997, pp. 124-133
In mammalian tissues, phosphatidylcholine, or 1,2-diacyl-glycerophosph
ocholine (GPC), is the most abundant form of choline-containing phosph
olipids. In some electrically active tissues, a significant portion of
the choline-containing phospholipids is 1-alkenyl-2-acyl-GPC (plasmen
ylcholine). The 1-alkyl-2-acyl-GPC is found in significant amounts in
circulating cells such as neutrophils and macrophages but in low amoun
ts in other tissues. Structural studies of phosphatidylcholine indicat
e that there is an asymmetric distribution of acyl groups on the molec
ule. Saturated fatty acids are usually esterified at the sn-1 position
of the glycerol backbone, whereas unsaturated fatty acids are esterif
ied at the sn-2 position. Similarly, unsaturated acyl groups are usual
ly found in the sn-2 position of plasmenylcholine. The remodelling of
the sn-2 acyl group in phosphatidylcholine by the deacylation-reacylat
ion process has been demonstrated in a number of tissues. Phospholipas
e A(2) is responsible for the hydrolysis of the acyl group at the sn-2
position, whereas 1-acyl-GPC acyl-CoA acyltransferase is responsible
for the reacylation reaction. The acyltransferase is located in the mi
crosomal fraction and displays specificity towards the polyunsaturated
acyl groups. The enzyme can be solubilized by detergent, but the enzy
me activity in soluble form is difficult to maintain. The acyltransfer
ase for the reacylation of 1-alkenyl-GPC is also located in the micros
omal fraction and is somewhat specific towards polyunsaturated acyl gr
oups. In guinea pig heart mitochondria, however, a new form of 1-alken
yl-GPC acyltransferase was identified which appeared to be different f
rom the microsomal form. The acyltransferase for the acylation of 1-al
kyl-GPC into platelet-activating factor has been studied in several ti
ssues including human neutrophils. At present, the contribution of the
acyltransferase in attaining the observed molecular composition of th
e choline-containing phospholipids in the tissue has not been defined.
We postulate that the intrinsic acyl-CoA specificity of the acyltrans
ferase, the flux of 1-acyl-GPC, 1-alkenyl-GPC and 1-alkyl-GPC, as well
as the pool size of acyl-CoA are major factors in producing the final
composition of the molecular species of the choline-containing phosph
olipids. (C) 1997 Elsevier Science B.V.