Essential role for MFG-E8 as ligand for alphavbeta5 integrin in diurnal retinal phagocytosis

Proc Natl Acad Sci U S A. 2007 Jul 17;104(29):12005-10. doi: 10.1073/pnas.0704756104. Epub 2007 Jul 9.

Abstract

The integrin receptor alphavbeta5 controls two independent forms of interactions of the retinal pigment epithelium (RPE) with adjacent photoreceptor outer segments that are essential for vision. Alphavbeta5 localizes specifically to apical microvilli of the RPE and contributes to retinal adhesion that maintains RPE contacts with intact outer segments at all times. Additionally, alphavbeta5 synchronizes diurnal bursts of RPE phagocytosis that clear photoreceptor outer segment fragments (POS) shed in a circadian rhythm. Dependence of retinal phagocytosis and adhesion on alphavbeta5 receptors suggests that the extracellular matrix ensheathing RPE microvilli contains ligands for this integrin. Here we studied mice lacking expression of functional MFG-E8 to test the contribution of this integrin ligand to alphavbeta5 functions in the retina. Lack of MFG-E8 only minimally reduced retinal adhesion. In contrast, lack of MFG-E8, like lack of alphavbeta5 receptor, eliminated alphavbeta5 downstream signaling involving the engulfment receptor MerTK and peak POS phagocytosis, both of which follow light onset in wild-type retina. MFG-E8-deficient RPE in primary culture retained normal epithelial morphology and levels of apical alphavbeta5 receptors, but showed impaired binding and engulfment of isolated POS. Soluble or POS-bound recombinant MFG-E8 was sufficient to fully restore phagocytosis by MFG-E8-deficient RPE. Furthermore, MFG-E8 supplementation strongly increased POS binding by wild-type and MerTK-deficient RPE, but did not affect POS binding by RPE lacking alphavbeta5. Thus, MFG-E8 stimulates rhythmic POS phagocytosis by ligating apical alphavbeta5 receptors of the RPE. These results identify MFG-E8 as the first extracellular ligand in the retina that is essential for diurnal POS phagocytosis.

Publication types

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

MeSH terms

  • Animals
  • Antigens, Surface / metabolism*
  • Cell Adhesion
  • Circadian Rhythm*
  • Enzyme Activation
  • Integrins / metabolism*
  • Ligands
  • Mice
  • Milk Proteins / metabolism*
  • Mutant Proteins / metabolism
  • Phagocytosis*
  • Phenotype
  • Pigment Epithelium of Eye / cytology
  • Protein Binding
  • Proto-Oncogene Proteins / metabolism
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Receptors, Vitronectin / metabolism*
  • Recombinant Proteins / metabolism
  • Rod Cell Outer Segment / cytology*
  • Rod Cell Outer Segment / metabolism*
  • Solubility
  • c-Mer Tyrosine Kinase

Substances

  • Antigens, Surface
  • Integrins
  • Ligands
  • Mfge8 protein, mouse
  • Milk Proteins
  • Mutant Proteins
  • Proto-Oncogene Proteins
  • Receptors, Vitronectin
  • Recombinant Proteins
  • integrin alphaVbeta5
  • Mertk protein, mouse
  • Receptor Protein-Tyrosine Kinases
  • c-Mer Tyrosine Kinase