Lcl. Silveira et al., THE GANGLION-CELL RESPONSE TO OPTIC-NERVE INJURY IN THE CAT - DIFFERENTIAL RESPONSES REVEALED BY NEUROFIBRILLAR STAINING, Journal of neurocytology, 23(2), 1994, pp. 75-86
The early responses of cat retinal ganglion cells to axotomy have been
examined using neurofibrillar and Nissl-stained wholemounts. We were
interested to learn whether the enhanced neurofilament expression, see
n in a number of neuronal systems, was also present in different neuro
nal populations of the cat retina and could be used to study the distr
ibution of these cells. We found that beta ganglion cells degenerate v
ery rapidly after axotomy with the nuclei becoming pyknotic within a f
ew days. Few beta cells showed increased neurofibrillar staining of th
e dendrites. The cell body degenerated prior to any visible degenerati
ve changes in the axon. A proportion of the alpha and gamma ganglion c
ells degenerated in the first two to three weeks after axotomy. The al
pha cells underwent markedly enhanced neurofibrillar staining of their
dendrites prior to degeneration. The Nissl material of the cell bodie
s diminished as the cells degenerated but we have not observed pyknoti
c nuclei. The dendritic trees of some axotomised gamma cells were also
revealed by the neurofibrillar stain three weeks after axotomy. These
results show that retinal ganglion cells do not degenerate by a dying
back process. We suggest that the rapid degeneration of the beta gang
lion cell population comes about by excitotoxic cell death, a conseque
nce of their large glutamatergic input from bipolar cells. The degener
ating beta ganglion cells have the morphological appearance of cells u
ndergoing apoptosis.