Be. Reese et Sf. Geller, PRECOCIOUS INVASION OF THE OPTIC STALK BY TRANSIENT RETINOPETAL AXONS, Journal of comparative neurology, 353(4), 1995, pp. 572-584
This study demonstrates that the fetal optic nerve contains a conspicu
ous population of transient retinopetal axons. Implants of the carbocy
anine dye, DiI, were made into the retina or diencephalon of fetal fer
rets to label the retinopetal axons retrogradely or anterogradely, res
pectively, and sections were immunostained for P-tubulin to label the
early differentiating axons in the optic nerve. Dye implants into the
optic nerve head, but not the retinal periphery, retrogradely labeled
somata in the ventrolateral diencephalon, provided the implants were m
ade before embryonic day (E) 30. When dye implants were made into the
ventrolateral diencephalon, these same retinopetal axons were anterogr
adely labeled, coursing through the optic nerve but never invading the
retina. The axons course as 2-5 fascicles from their cells of origin
and turn laterally to enter the optic nerve where it joins the future
hypothalamus. The retinopetal cells can be retrogradely labeled as ear
ly as E20, before optic axons have left the retina. The optic nerve an
d fiber layer are immunoreactive for beta-tubulin on E24 and thereafte
r, whereas on E20 and E22, they are immunonegative. Yet at these early
embryonic ages, immunopositive fascicles of axons course from the die
ncephalon into the optic stalk, confirming the precocious nature of th
e retinopetal projection. Implants of dye made into the future optic n
erve head at these very early stages also retrogradely label retinopet
al cells in the future chiasmatic region. These cells are distributed
primarily on the side ipsilateral to the midline, but a few can be fou
nd contralateral to it. Both these, as well as the retinopetal axons a
rising from the ventrolateral diencephalon, may serve a transient guid
ance function for later developing optic axons. (C) 1995 Wiley-Liss, I
nc.