Effect of bacterial endotoxin on the in vitro release of type II phospholipase-A(2) and prostaglandin E-2 from human placenta

Citation
W. Farrugia et al., Effect of bacterial endotoxin on the in vitro release of type II phospholipase-A(2) and prostaglandin E-2 from human placenta, J ENDOCR, 160(2), 1999, pp. 291-296
Citations number
31
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF ENDOCRINOLOGY
ISSN journal
00220795 → ACNP
Volume
160
Issue
2
Year of publication
1999
Pages
291 - 296
Database
ISI
SICI code
0022-0795(199902)160:2<291:EOBEOT>2.0.ZU;2-X
Abstract
The aim of this study was to establish the effect of bacterial endotoxin li popolysaccharide (LPS) on the release of Type II phospholipase-A(2) (PLA(2) ) and prostaglandin E-2 (PCE2) from late-pregnant human placental tissue in cubated in vitro. Under basal conditions, immunoreactive Type II PLA(2) and PGE(2) were released from tissue explants in a time-dependent manner (up t o 24 h, ANOVA, P<0.0001, n=6). The release of these mediators was not assoc iated with a loss of cell membrane integrity, as indicated by concentration s of the intracellular enzyme, lactate dehydrogenase (LDH), in the incubati on medium. Incubation of explants in the presence of LPS (0.001-100 mu g LP S/ml) significantly decreased PLA(2) tissue content (P<0.02, n=6) and incre ased the accumulation of PLA(2) and PGE(2) in the incubation medium (P<0.00 01, n=6). The data obtained in this study indicated that Type II PLA(2) and PGE(2) are released from term placenta under basal conditions and that LPS stimulated their release. The associated decrease in PLA(2) tissue content is consistent with the hypothesis that LPS induces the release of stored P LA(2). This study identifies one pathway by which products of bacterial inf ection may induce the release of a pro-inflammatory, extracellularly active PLA(2) from intrauterine tissues that may promote the formation of phospho lipid metabolites involved in the process of labour and delivery (e.g. the prostaglandins).