4.7 Article

Influences of Glaucoma on the Structure and Function of Synapses in the Visual System

Journal

ANTIOXIDANTS & REDOX SIGNALING
Volume 37, Issue 10-12, Pages 842-861

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/ars.2021.0253

Keywords

glaucoma; neurodegeneration; synapse; retina; vision; axon; mitochondria

Funding

  1. NIH [R01 EY030507]
  2. University of Nebraska

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Glaucoma is an age-related neurodegenerative disorder associated with sensitivity to intraocular pressure. It is the leading cause of irreversible vision loss worldwide, resulting from damage to the retinal ganglion cells. Glaucoma affects different populations of these cells to varying extents and along distinct time courses, and its effects on synaptic function and vulnerability of the cells are still not fully understood. Further research is needed to determine the underlying mechanisms and to develop diagnostic and therapeutic approaches.
Significance: Glaucoma is an age-related neurodegenerative disorder of the visual system associated with sensitivity to intraocular pressure (IOP). It is the leading irreversible cause of vision loss worldwide, and vision loss results from damage and dysfunction of the retinal output neurons known as retinal ganglion cells (RGCs).Recent Advances: Elevated IOP and optic nerve injury triggers pruning of RGC dendrites, altered morphology of excitatory inputs from presynaptic bipolar cells, and disrupted RGC synaptic function. Less is known about RGC outputs, although evidence to date indicates that glaucoma is associated with altered mitochondrial and synaptic structure and function in RGC-projection targets in the brain. These early functional changes likely contribute to vision loss and might be a window into early diagnosis and treatment.Critical Issues: Glaucoma affects different RGC populations to varying extents and along distinct time courses. The influence of glaucoma on RGC synaptic function as well as the mechanisms underlying these effects remain to be determined. Since RGCs are an especially energetically demanding population of neurons, altered intracellular axon transport of mitochondria and mitochondrial function might contribute to RGC synaptic dysfunction in the retina and brain as well as RGC vulnerability in glaucoma.Future Directions: The mechanisms underlying differential RGC vulnerability remain to be determined. Moreover, the timing and mechanisms of RGCs synaptic dysfunction and degeneration will provide valuable insight into the disease process in glaucoma. Future work will be able to capitalize on these findings to better design diagnostic and therapeutic approaches to detect disease and prevent vision loss.

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