Investigative Ophthalmology & Visual Science Cover Image for Volume 57, Issue 12
September 2016
Volume 57, Issue 12
Open Access
ARVO Annual Meeting Abstract  |   September 2016
Pigment epithelium-derived factor (PEDF) prevents apoptosis and promotes apical localization of opsin in retina photoreceptors
Author Affiliations & Notes
  • S Patricia Becerra
    NEI-NIH, Bethesda, Maryland, United States
  • Germán Michelis
    Instituto de Investigaciones Bioquímicas (INIBIBB) , Universidad Nacional del Sur (UNS)-CONICET, Bahia Blanca, Argentina
  • Lorena Germán
    Instituto de Investigaciones Bioquímicas (INIBIBB) , Universidad Nacional del Sur (UNS)-CONICET, Bahia Blanca, Argentina
  • Nora Patricia Rotstein
    Instituto de Investigaciones Bioquímicas (INIBIBB) , Universidad Nacional del Sur (UNS)-CONICET, Bahia Blanca, Argentina
  • Luis Politi
    Instituto de Investigaciones Bioquímicas (INIBIBB) , Universidad Nacional del Sur (UNS)-CONICET, Bahia Blanca, Argentina
  • Footnotes
    Commercial Relationships   S Patricia Becerra, None; Germán Michelis, None; Lorena Germán, None; Nora Rotstein, None; Luis Politi, None
  • Footnotes
    Support  The Intramural Research Program of the NEI-NIH; and ANPCYT, CONICET and Universidad Nacional del Sur (to LEP)
Investigative Ophthalmology & Visual Science September 2016, Vol.57, 188. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      S Patricia Becerra, Germán Michelis, Lorena Germán, Nora Patricia Rotstein, Luis Politi; Pigment epithelium-derived factor (PEDF) prevents apoptosis and promotes apical localization of opsin in retina photoreceptors. Invest. Ophthalmol. Vis. Sci. 2016;57(12):188.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose : PEDF plays a critical role in promoting survival of photoreceptors and in an R28 retinal progenitor cell line by binding to PEDF membrane receptors. However, the intracellular mechanisms it activates in retinal neurons remain to be established. In the present work, we investigated the effects of PEDF in developing retina neurons in culture.

Methods : Pure neuronal cultures were prepared from retinas ofrats at post-natal day 1. Recombinant human PEDF was purified from media of BHK cells stably transfected with expression vectors containing the full-length PEDF cDNA. Rod photoreceptors and amacrine neurons were grown in chemically defined medium supplemented at day 3 in culture with either PEDF (10 nM); PEDF plus P1 blocking peptide (100nM); or vehicle (control) and fixed at days 5 or 6 in culture. Apoptosis, cell death, mitochondrial activity, opsin expression and localization and axonal outgrowth in vitro were then determined.

Results : PEDF enhanced the survival of photoreceptors with time in culture compared to controls, as determined by Propidium Iodide and TUNEL assays. PEDF-mediated prevention of apoptosis involved the preservation of mitochondrial membrane potential. Pre-incubation of PEDF with P1, a PEDF receptor blocking peptide, completely abolished PEDF effects on survival. PEDF did not increase opsin expression but promoted apical localization of opsin, compared to its diffuse distribution in controls, resembling what occurs in mature retinas. Interestingly, PEDF also stimulated axon outgrowth in amacrine neurons, since axonal length doubled in these neurons in PEDF-supplemented cultures, compared to controls.

Conclusions : In summary, this work suggests that PEDF is an effective survival factor for retinal photoreceptors during development in vitro. It also implies that PEDF plays different roles in neuronal differentiation, promoting the localization of opsin in apical processes and stimulating axonal outgrowth in amacrine neurons.

This is an abstract that was submitted for the 2016 ARVO Annual Meeting, held in Seattle, Wash., May 1-5, 2016.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×