Identification of a lipase-linked cell membrane receptor for pigment epithelium-derived factor

J Biol Chem. 2006 Dec 8;281(49):38022-37. doi: 10.1074/jbc.M600353200. Epub 2006 Oct 10.


Pigment epithelium-derived factor (PEDF) is an extracellular multifunctional protein belonging to the serpin superfamily with demonstrable neurotrophic, gliastatic, neuronotrophic, antiangiogenic, and antitumorigenic properties. We have previously provided biochemical evidence for high affinity PEDF-binding sites and proteins in plasma membranes of retina, retinoblastoma, and CNS cells. This study was designed to reveal a receptor involved in the biological activities of PEDF. Using a yeast two-hybrid screening, we identified a novel gene from pigment epithelium of the human retina that codes for a PEDF-binding partner, which we term PEDF-R. The derived polypeptide has putative transmembrane, intracellular and extracellular regions, and a phospholipase domain. Recently, PEDF-R (TTS-2.2/independent phospholipase A(2) (PLA(2))zeta and mouse desnutrin/ATGL) has been described in adipose cells as a member of the new calcium-independent PLA(2)/nutrin/patatin-like phospholipase domain-containing 2 (PNPLA2) family that possesses triglyceride lipase and acylglycerol transacylase activities. Here we describe the PEDF-R gene expression in the retina and its heterologous expression by bacterial and eukaryotic systems, and we demonstrate that its protein product has specific and high binding affinity for PEDF, has a potent phospholipase A(2) activity that liberates fatty acids, and is associated with eukaryotic cell membranes. Most importantly, PEDF binding stimulates the enzymatic phospholipase A(2) activity of PEDF-R. In conclusion, we have identified a novel PEDF-R gene in the retina for a phospholipase-linked membrane protein with high affinity for PEDF, suggesting a molecular pathway by which ligand/receptor interaction on the cell surface could generate a cellular signal.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell Line
  • DNA Primers / genetics
  • Eye Proteins / genetics
  • Eye Proteins / metabolism*
  • Humans
  • In Vitro Techniques
  • Mice
  • Molecular Sequence Data
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism*
  • Phospholipases A / genetics
  • Phospholipases A / metabolism*
  • Pigment Epithelium of Eye / metabolism
  • Receptors, Neuropeptide / genetics
  • Receptors, Neuropeptide / metabolism*
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Serpins / genetics
  • Serpins / metabolism*
  • Two-Hybrid System Techniques


  • DNA Primers
  • Eye Proteins
  • Nerve Growth Factors
  • Receptors, Neuropeptide
  • Recombinant Proteins
  • Serpins
  • pigment epithelium-derived factor
  • pigment epithelium-derived factor receptor
  • Phospholipases A