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Journal of Neuroscience, Vol 15, 6389-6402, Copyright © 1995 by Society for Neuroscience
The first retinal axon growth in the mouse optic chiasm: axon patterning and the cellular environment
RC Marcus and CA Mason
Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
The retinofugal pathway is a useful model for axon guidance because fibers
from each eye project to targets on both sides of the brain. Studies using
static and real time analyses in mice at E15-17 demonstrated that uncrossed
axons from ventrotemporal retina diverge from crossed axons in the optic
chiasm, where specialized resident cells may direct divergence. Other
studies, however, suggest that pioneering uncrossed retinal axons derive
from a different retinal region, take a different course, and enter the
ipsilateral optic tract independent of fiber-fiber interactions. We examine
these differences by dye-labeling the earliest optic axons and
immunocytochemically identifying cells in their path. The first optic axons
arising from dorsocentral retina, enter the diencephalon at E12.5. All
axons initially grow caudally, lateral to a radial glial palisade. In
contrast to later growing axons, early uncrossed axons enter the
ipsilateral optic tract directly. Crossed axons enter the glial palisade
and course medially, then anteriorly, in a pathway corresponding to the
border of an early neuronal population that expresses SSEA-1, CD44, and
beta-tubulin. Axon patterning occurs independent of fiber-fiber
interactions from both eyes, as the first uncrossed axons enter the optic
tract before crossed ones from opposite eye. These analysis, in conjunction
with our previous studies during the principal period of retinal axon
growth in the diencephalon, suggest that the adult visual projection arises
from age-dependent variations in the types and relative contribution of
cues along the path through the emerging optic chiasm.
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