Clearance of group X secretory phospholipase A(2) via mouse phospholipase A(2) receptor

FEBS Lett. 2001 Dec 7;509(2):250-4. doi: 10.1016/s0014-5793(01)03173-8.

Abstract

Given the potent hydrolyzing activity toward phosphatidylcholine, group X secretory phospholipase A(2) (sPLA(2)-X) elicits a marked release of arachidonic acid linked to the potent production of lipid mediators in various cell types. We have recently shown that sPLA(2)-X can also act as a ligand for mouse phospholipase A(2) receptor (PLA(2)R). Here, we found that sPLA(2)-X was internalized and degraded via binding to PLA(2)R associated with the diminished prostaglandin E(2) (PGE(2)) formation in PLA(2)R-expressing Chinese hamster ovary (CHO) cells compared to CHO cells. Indirect immunocytochemical analysis revealed that internalized sPLA(2)-X was co-localized with PLA(2)R in the punctate structures in PLA(2)R-expressing CHO cells. Moreover, in mouse osteoblastic MC3T3-E(1) cells that endogenously express the PLA(2)R, the internalized sPLA(2)-X was localized in lysosomes. These findings demonstrate that PLA(2)R acts as a clearance receptor for sPLA(2)-X to suppress its strong enzymatic activity.

MeSH terms

  • 3T3 Cells
  • Animals
  • Biological Transport
  • CHO Cells
  • Cricetinae
  • Dinoprostone / biosynthesis
  • Group X Phospholipases A2
  • Lysosomes / metabolism
  • Metabolic Clearance Rate
  • Mice
  • Phospholipases A / metabolism*
  • Receptors, Cell Surface / metabolism*
  • Receptors, Phospholipase A2

Substances

  • Pla2r1 protein, mouse
  • Receptors, Cell Surface
  • Receptors, Phospholipase A2
  • Phospholipases A
  • Group X Phospholipases A2
  • Pla2g10 protein, mouse
  • Dinoprostone