AI Article Synopsis

  • Retinal ganglion cells (RGC) are at risk of death in various vision-related conditions like glaucoma and ischemic retinopathies.
  • Pigment epithelium-derived factor (PEDF), produced by Müller cells in the retina, plays a vital role in protecting RGCs from ischemic damage.
  • In experiments, PEDF treatment improved RGC survival under hypoxic conditions, and blocking PEDF reduced the protective effects of Müller cells, indicating its importance in retinal cell health.

Article Abstract

Survival of retinal ganglion cells (RGC) is compromised in several vision-threatening disorders such as ischemic and hypertensive retinopathies and glaucoma. Pigment epithelium-derived factor (PEDF) is a naturally occurring pleiotropic secreted factor in the retina. PEDF produced by retinal glial (Müller) cells is suspected to be an essential component of neuron-glial interactions especially for RGC, as it can protect this neuronal type from ischemia-induced cell death. Here we show that PEDF treatment can directly affect RGC survival in vitro. Using Müller cell-RGC-co-cultures we observed that activity of Müller-cell derived soluble mediators can attenuate hypoxia-induced damage and RGC loss. Finally, neutralizing the activity of PEDF in glia-conditioned media partially abolished the neuroprotective effect of glia, leading to an increased neuronal death in hypoxic condition. Altogether our results suggest that PEDF is crucially involved in the neuroprotective process of reactive Müller cells towards RGC.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368109PMC
http://dx.doi.org/10.1007/s11064-012-0747-8DOI Listing

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