We have previously shown that the mature optic chiasm of a marsupial i
s divided morphologically into three regions, two lateral regions in w
hich ipsilaterally projecting axons are confined and a central region
containing only contralaterally projecting axons. By contrast, in the
chiasms of eutherian (placental) mammals studied to date, there is no
tripartite configuration. Ipsilaterally and contralaterally projecting
axons from each eye are mixed in the caudal nerve and in each hemichi
asm and encounter axons from the opposite eye near the midline of the
chiasm. Here, we show that, unlike eutherians, marsupials have astrocy
tic processes in high concentrations in lateral regions of the nerve a
nd rostral chiasm. Early in development, during the period when optic
axons are growing through the chiasm, many intrachiasmatic cells are s
een with densities five to eight times higher in lateral than in centr
al chiasmatic regions. Such cells continue to be added to all chiasmat
ic regions; later in development, considerably more are added centrall
y, as the chiasm increases in volume. In the mature chiasm, cell densi
ties are similar in all regions. By contrast to the marsupial, cell ad
dition in the chiasm of a placental mammal, the ferret, is almost enti
rely restricted to later developmental stages, after axons have grown
through the chiasm, and there are no obvious spatial variations in the
distribution of cells during the period examined. During development,
similar to the adult marsupial, ipsilaterally projecting axons do not
approach the chiasmatic midline but remain confined laterally. We pro
pose that the cells generated early and seen in high densities in the
lateral chiasmatic regions of the marsupial may play a role in guiding
retinal axons through this region of pathway selection. These data su
ggest that there is not a common pattern of developmental mechanisms t
hat control the path of axons through the chiasm of different mammals.
(C) 1995 Wiley-Liss, Inc.