July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
MAP4K4 and GSK-3 pathways complement DLK/LZK signaling to control cell death and axon degeneration in retinal ganglion cells
Author Affiliations & Notes
  • Amit K Patel
    Ophthalmology, University of California San Diego, La Jolla, California, United States
  • Katy Mitchell
    Ophthalmology, Wilmer Eye Institute, Johns Hopkins University, Maryland, United States
  • Baranda S. Hansen
    Ophthalmology, Wilmer Eye Institute, Johns Hopkins University, Maryland, United States
  • Cindy Berlinicke
    Ophthalmology, Wilmer Eye Institute, Johns Hopkins University, Maryland, United States
  • Risa Broyer
    Ophthalmology, University of California San Diego, La Jolla, California, United States
  • Donald J Zack
    Ophthalmology, Wilmer Eye Institute, Johns Hopkins University, Maryland, United States
  • Derek Stuart Welsbie
    Ophthalmology, University of California San Diego, La Jolla, California, United States
  • Footnotes
    Commercial Relationships   Amit Patel, None; Katy Mitchell, None; Baranda Hansen, None; Cindy Berlinicke, None; Risa Broyer, None; Donald Zack, None; Derek Welsbie, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 2255. doi:
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      Amit K Patel, Katy Mitchell, Baranda S. Hansen, Cindy Berlinicke, Risa Broyer, Donald J Zack, Derek Stuart Welsbie; MAP4K4 and GSK-3 pathways complement DLK/LZK signaling to control cell death and axon degeneration in retinal ganglion cells. Invest. Ophthalmol. Vis. Sci. 2019;60(9):2255.

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

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Abstract

Purpose : Axonal injury induced death of retinal ganglion cells (RGCs) is a hallmark of glaucoma. We previously developed an RNA interference-based functional genomic screen in RGCs to discover neuroprotective targets. From this screen, we identified dual leucine zipper kinase (DLK) and leucine zipper kinase (LZK) signaling as a key pathway that regulates RGC cell death. While inhibiting DLK/LZK results in robust protection of RGCs, there is room for improvement. Furthermore DLK/LZK inhibition does not prevent axon degeneration. Therefore, we performed a complementary small molecule screen using a library of highly-profiled protein kinase inhibitors (PKIs) to identify if there are complementary pathway targets which could improve RGC survival and protect axons.

Methods : We conducted a high-throughput small molecule screen in primary mouse RGCs using the Glaxo-Smith-Kline Protein Kinase Inhibitor Set (PKIS1). Using published kinase profiling of these compounds and the survival results from the screen, we can bioinformatically deconvolute which specific kinase(s) have a role in RGC death. We tested the positive hits for interactions with the DLK/LZK pathway and in their ability to prevent axon degeneration, using microtubule destabilization as a proxy for cell and axon injury in vitro.

Results : In this screen, we identified glycogen synthase kinase three (GSK-3) and mitogen activated protein kinase kinase kinase kinase (MAP4K4) family members as targets whose inhibition leads to modest increases in RGC survival. Moreover, simultaneous inhibition of the GSK-3 and MAP4K4 pathways lead to a synergistic increase in RGC survival. As we already have identified the DLK/LZK pathway as a neuroprotective target, we wanted to see whether additionally targeting the MAP4K4/GSK-3 pathways could improve RGC survival. We found that the combined inhibition of the GSK-3/MAP4K4/DLK/LZK pathways resulted in near complete protection of RGCs. Furthermore, we found that MAP4K4/GSK-3 inhibition also protects against axonal degeneration in our model, in addition to increasing RGC survival.

Conclusions : MAP4K4/GSK-3 and DLK/LZK have complementary signaling pathways that interact to control cell death/survival and axon protection in RGCs. Furthermore, these results establish combinatorial kinase targeting as a robust neuroprotective strategy for optic neuropathies.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

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