Neuropeptide Y-evoked proliferation of retinal glial (Muller) cells

Graefes Arch Clin Exp Ophthalmol. 2004 Nov;242(11):944-50. doi: 10.1007/s00417-004-0954-3. Epub 2004 Aug 4.


Background: Glial cells in human retinas and in fibrocellular membranes from patients with proliferative vitreoretinopathy (PVR) have been described to upregulate their expression of Y1 receptors for neuropeptide Y (NPY) (Soler et al.: Glia 39:320, 2002). However, it is unknown whether Y1 receptor activation causes proliferation of retinal glial cells. We investigated whether NPY exerts a proliferation-stimulating effect on retinal glial cells, and compared the NPY-evoked signaling with the signaling of purinergic P2Y receptors.

Methods: Proliferation assays using bromodeoxyuridine were carried out on primarily cultured Muller glial cells of the guinea pig, in the absence and presence of blockers of Y1 receptors, of receptor tyrosine kinases (RTKs), of mitogen-activated protein kinases (MAPKs) and of phosphatidylinositol-3 kinase (PI3K).

Results: NPY exerted a biphasic effect on Muller cell proliferation. At low concentrations (0.1 ng/ml and 1 ng/ml) it decreased the proliferation rate of the cells, while at higher concentration (100 ng/ml) it increased Muller cell proliferation. The NPY-evoked proliferation was mediated by Y1 receptor stimulation and by activation of the p44/p42 MAPKs and partially of the p38 MAPK. Moreover, Y1 receptor-induced activation of PI3K as well as transactivations of the platelet-derived and the epidermal growth factor RTKs were necessary for full mitogenic effect of NPY. Y1 and P2Y receptors share partially common signal transduction pathways in Muller cells.

Conclusion: It is suggested that NPY may be involved in stimulation of retinal glial cell proliferation during PVR when it is released at higher amounts into the injured retina.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Animals
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • DNA / biosynthesis
  • Fluorescent Antibody Technique, Indirect
  • Glial Fibrillary Acidic Protein / metabolism
  • Guinea Pigs
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Neuroglia / cytology*
  • Neuropeptide Y / pharmacology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Receptors, Neuropeptide Y / metabolism*
  • Receptors, Purinergic P2 / metabolism
  • Retina / cytology*
  • p38 Mitogen-Activated Protein Kinases / metabolism


  • Glial Fibrillary Acidic Protein
  • Neuropeptide Y
  • Receptors, Neuropeptide Y
  • Receptors, Purinergic P2
  • neuropeptide Y-Y1 receptor
  • Adenosine Triphosphate
  • DNA
  • Phosphatidylinositol 3-Kinases
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • p38 Mitogen-Activated Protein Kinases