4.6 Article

Bax Contributes to Retinal Ganglion Cell Dendritic Degeneration During Glaucoma

Journal

MOLECULAR NEUROBIOLOGY
Volume 59, Issue 3, Pages 1366-1380

Publisher

SPRINGER
DOI: 10.1007/s12035-021-02675-5

Keywords

Bcl2-associated X protein; Bax(-/ -); Neuroprotection; Neurodegeneration; Glaucoma; Retinal ganglion cells; Dendritic morphology; Axonopathy

Categories

Funding

  1. Research to Prevent Blindness Inc.
  2. Stein Innovation Award
  3. Stanley Cohen Innovation Fund
  4. National Institutes of Health [EY017427, EY024997, EY008126, CA68485, DK20593, DK58404, DK59637]
  5. Vanderbilt University Medical Center Cell Imaging Shared Resource core facility
  6. NIH [CA68485, DK20593, DK58404, DK59637]

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Bax contributes to RGC dendritic degeneration and distinguishes the proximal and distal neurodegenerative programs involved during the progression of glaucoma.
The BCL-2 (B-cell lymphoma-2) family of proteins contributes to mitochondrial-based apoptosis in models of neurodegeneration, including glaucomatous optic neuropathy (glaucoma), which degrades the retinal ganglion cell (RGC) axonal projection to the visual brain. Glaucoma is commonly associated with increased sensitivity to intraocular pressure (IOP) and involves a proximal program that leads to RGC dendritic pruning and a distal program that underlies axonopathy in the optic projection. While genetic deletion of the Bcl2-associated X protein (Bax(-/-)) prolongs RGC body survival in models of glaucoma and optic nerve trauma, axonopathy persists, thus raising the question of whether dendrites and the RGC light response are protected. Here, we used an inducible model of glaucoma in Bax(-/-) mice to determine if Bax contributes to RGC dendritic degeneration. We performed whole-cell recordings and dye filling in RGCs signaling light onset (alpha ON-Sustained) and offset (alpha OFF-Sustained). We recovered RGC dendritic morphologies by confocal microscopy and analyzed dendritic arbor complexity and size. Additionally, we assessed RGC axon function by measuring anterograde axon transport of cholera toxin subunit B to the superior colliculus and behavioral spatial frequency threshold (i.e., spatial acuity). We found 1 month of IOP elevation did not cause significant RGC death in either WT or Bax(-/-) retinas. However, IOP elevation reduced dendritic arbor complexity of WT alpha ON-Sustained and alpha OFF-Sustained RGCs. In the absence of Bax, alpha ON- and alpha OFF-Sustained RGC dendritic arbors remained intact following IOP elevation. In addition to dendrites, neuroprotection by Bax(-/-) generalized to alpha ON-and alpha OFF-Sustained RGC light- and current-evoked responses. Both anterograde axon transport and spatial acuity declined during IOP elevation in WT and Bax(-/-) mice. Collectively, our results indicate Bax contributes to RGC dendritic degeneration and distinguishes the proximal and distal neurodegenerative programs involved during the progression of glaucoma.

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