GLUTAMATE toxicity in retinal ganglion cells has been well documented
both in vitro and in vitro, and may play a role in both normal neurona
l development and a variety of pathological states. Glutamate receptor
s are found on cell bodies and neuronal processes, both axons and dend
rites. Other work has suggested that one or more of these locales may
play a more pronounced role in glutamate-mediated toxicity. We now rep
ort that N-methyl-D-aspartate (NMDA) is more toxic to retinal ganglion
cells with neurites. Cells without neurites were relatively unaffecte
d by glutamate or NMDA. Cells with longer neurites or more neurite bra
nch points were more likely to sustain NMDA-mediated neurotoxicity. Th
ese observations suggest that glutamate-mediated loss may be mediated
through NMDA receptors found on neurites, rather than through a direct
effect on the cell body.