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. 2012 May 4;53(5):2482-4.
doi: 10.1167/iovs.12-9483i.

The cell and molecular biology of glaucoma: axonopathy and the brain

Affiliations

The cell and molecular biology of glaucoma: axonopathy and the brain

David J Calkins et al. Invest Ophthalmol Vis Sci. .
No abstract available

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Figures

Figure 1
Figure 1
Compartmentalized RGC degeneration in glaucoma. The axon of the RGC passes unmyelinated through the astrocyte-rich optic nerve head, an established site of vulnerability exhibiting glaucoma-related stressors such as glial reactivity. A contralateral projection is shown depicting the axon passing through the optic chiasm with terminals targeting the superior colliculus and other more anterior sites. These include the suprachiasmatic nucleus (SCN), lateral geniculate nucleus (LGN), and the pretectal nuclei: olivary pretectal (OPT), the nucleus of the optic tract (NOT), and the posterior pretectal (PPT). Degenerative events in glaucomatous axonopathy include failure of axonal transport, both anterograde (red arrow) and later retrograde (green arrow). RGC axon terminals and their synapses degrade later. Later, degeneration in the retina includes loss of excitatory synapses, dendritic pruning, and finally cell body loss (modified from Crish and Calkins).

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