April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Prolonged NMDA Stimulation Induces Neuroprotective Pathways and Enhances Survivability of Primary Retinal Ganglion Cells
Author Affiliations & Notes
  • Brett H Mueller
    Pharmacology & Neuroscience, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
    North Texas Eye Research Institute, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
  • Yong H Park
    Pharmacology & Neuroscience, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
    North Texas Eye Research Institute, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
  • Hai-Ying Ma
    Pharmacology & Neuroscience, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
    North Texas Eye Research Institute, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
  • Thomas Yorio
    Pharmacology & Neuroscience, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
    North Texas Eye Research Institute, Univ of North Texas Hlth Sci Ctr, Fort Worth, TX
  • Footnotes
    Commercial Relationships Brett Mueller, None; Yong Park, None; Hai-Ying Ma, None; Thomas Yorio, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 1903. doi:
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      Brett H Mueller, Yong H Park, Hai-Ying Ma, Thomas Yorio; Prolonged NMDA Stimulation Induces Neuroprotective Pathways and Enhances Survivability of Primary Retinal Ganglion Cells. Invest. Ophthalmol. Vis. Sci. 2014;55(13):1903.

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

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Abstract

Purpose: Calcium influx through postsynaptic NMDA receptors has been shown to stimulate a number of key pro-survival genes; however, prolonged stimulation has been shown to have excitotoxic effects leading to apoptosis in neurons. Previous studies have shown a rapid dephosphorylation of CREB in primary hippocampal neurons treated for 1-2 hours with100µM NMDA. It is hypothesized that the activation of CREB-specific phosphatases is one of the main pathways that cause apoptosis during NMDA excitotoxicity. The current study investigated the role of NMDA stimulation on the phosphorylation of CREB in primary RGCs, and assessed if NMDA overstimulation caused excitotoxic changes similar to those seen in primary hippocampal neurons. The occurrence of NMDA excitotoxicity in bipolar and photoreceptor cells was also investigated.

Methods: Purification and culture of RGCs were performed by sequential immunopanning using Thy 1.1 antibody from P3-P7 Sprague-Dawley rats. Mixed retinal cultures that remained following isolation of RGCs from the retina were plated once the RGCs were separated and purified. Western blots were performed to determine signaling pathways linked to NMDA induced cell survival or excitotoxicity. Calcein AM and ethidium homodimer were used to quantify cell survival and cell death. Cells were also subjected to a trophic factor deprivation insult for 6 hours and 24 hours.

Results: Treatment of primary RGCs with NMDA (100 µM) for 6 hours caused a greater than 2-3 fold induction of the transcription factor pCREB. MK801 (NMDA antagonist) completely abolished endogenous levels of pCREB and blocked NMDA induction of pCREB. NMDA (100 µM) treatment for 6 and 24 hours under trophic factor deprivation, protected RGCs from trophic factor deprivation induced cellular death. The mixed retinal cultures (retinal cells without RGCs) had an opposite effect, where the levels of pCREB were diminished and the neurons died when treated with 100 µM of NMDA.

Conclusions: The data suggests that NMDA signaling is essential for RGC survivability and blocking calcium ion influx through this receptor by the NMDA blocker, MK801, can be detrimental to RGC function and survival. These results also demonstrate that primary RGCs behave differently than other neurons in the retina, and are not susceptible to NMDA excitotoxicity.

Keywords: 518 excitatory neurotransmitters • 615 neuroprotection • 531 ganglion cells  
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