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Four Steps to Optic Nerve Regeneration

Journal

JOURNAL OF NEURO-OPHTHALMOLOGY
Volume 30, Issue 4, Pages 347-360

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/WNO.0b013e3181e755af

Keywords

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Funding

  1. NEI [EY020913, EY014801]
  2. NINDS [NS061348]
  3. Glaucoma Foundation
  4. American Heart Association
  5. James and Esther King Foundation
  6. Research to Prevent Blindness to the University of Miami
  7. National Institutes of Health [T32 NS07492, T32 NS007459]

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The failure of the optic nerve to regenerate after injury or in neurodegenerative disease remains a major clinical and scientific problem. Retinal ganglion cell (RGC) axons course through the optic nerve and carry all the visual information to the brain, but after injury, they fail to regrow through the optic nerve and RGC cell bodies typically die, leading to permanent loss of vision. There are at least 4 hurdles to overcome in preserving RGCs and regenerating their axons: 1) increase RGC survival, 2) overcome the inhibitory environment of the optic nerve, 3) enhance RGC intrinsic axon growth potential, and 4) optimize the mapping of RGC connections back into their targets in the brain.

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