Concentration of astrocytic filaments at the retinal optic nerve junction is coincident with the absence of intra-retinal myelination: comparative and developmental evidence
Y. Morcos et Tl. Chan-ling, Concentration of astrocytic filaments at the retinal optic nerve junction is coincident with the absence of intra-retinal myelination: comparative and developmental evidence, J NEUROCYT, 29(9), 2000, pp. 665-678
The structure of the lamina cribrosa (LC) and astrocytic density were exami
ned in various species with and without intra-retinal myelination. Sections
of optic nerve from various species were stained with Milligan's trichrome
or antibodies to glial fibrillary acidic protein, myelin basic protein (MB
P) and antibody O4. Marmoset, flying fox, cat, and sheep, which lack intrar
etinal myelination, were shown to possess a well-developed LC as well as a
marked concentration of astrocytic filaments distal to the LC. Rat and mous
e, which lack intraretinal myelination, lacked a well-developed LC but exhi
bited a marked concentration of astrocytic filaments in this region. Rabbit
and chicken, which exhibit intraretinal myelination, lacked both a well-de
veloped LC and a concentration of astrocytes at the retinal optic nerve jun
ction (ROJ). A marked concentration of astrocytes at the ROJ of human fetus
es was also apparent at 13 weeks of gestation, prior to myelination of the
optic nerve; in contrast, the LC was not fully developed even at birth. Thi
s concentration of astrocytes was located distal to O4 and MBP immunoreacti
vity in human optic nerve, and coincided with the site of initial myelinati
on of ganglion cell axons in marmoset and rat. Myelination proceeded from t
he chiasm towards the retinal end of the human optic nerve. Moreover, the o
uter limit of oligodendrocyte precursor cells (OPC) migration into the rabb
it retina was restricted by the outer limit of astrocyte spread. These obse
rvations indicate that a concentration of astrocytic filaments at the ROJ i
s coincident with the absence of intraretinal myelination. Differential exp
ression of tenascin-C by astrocytes at the ROJ appears to contribute to the
molecular barrier to OPC migration (see Bartsch et al., 1994), while expre
ssion of the homedomain protein Vax 1 by glial cells at the optic nerve hea
d appears to inhibit migration of retinal pigment epithelial cells into the
optic nerve (see Bertuzzi et al., 1999). These observations combined with
our present comparative and developmental data lead us to suggest that the
astrocytes at the ROJ serve to regulate cellular traffic into and out of th
e retina.