D. Aggounzouaoui et Gm. Innocenti, JUVENILE VISUAL CALLOSAL AXONS IN KITTENS DISPLAY ORIGIN-RELATED AND FATE-RELATED MORPHOLOGY AND DISTRIBUTION OF ARBORS, European journal of neuroscience, 6(12), 1994, pp. 1846-1863
In kittens, callosal axons originating either from medial area 17 (tra
nsient axons) or near the 17/18 border (mostly permanent axons) were l
abelled with anterogradely transported biocytin; they were reconstruct
ed by computer from serial sections, and their morphologies compared a
t different ages. During the first and second postnatal weeks both set
s of axons branched profusely in the white matter of the lateral gyrus
and the number of branches increased with age. The most common type o
f axon ending was the growth cone; others may have been collapsing gro
wth cones, branches in the process of elimination or early synaptic bo
utons. Axons from medial area 17 distributed over a broad territory, i
ncluding the 17/18 border where callosal axons terminate in the adult
cat, but without aiming specifically at any one area. The majority of
axons and their branches terminated in the white matter or at the bott
om of layer VI; exceptionally they extended further into the cortex. M
ost of the axons originating near the 17/18 border were different from
those described above, and the difference increased with age. Althoug
h they also terminated profusely in the white matter of the lateral gy
rus, most of the branches terminated near the contralateral 17/18 bord
er; they frequently entered the grey matter up to the superficial laye
rs and branched into it. During the third week, axons from medial area
17 were rarely found to extend beyond the corpus callosum, probably b
ecause they were in the process of being eliminated. In contrast, axon
s originating near the 17/18 border had increased their number of bran
ches in the grey matter. In conclusion, during the first and second po
stnatal weeks axons grew and differentiated according to their origin,
and this anticipated whether they would be maintained or eliminated.
Neurotrophic signals, possibly from the white matter or the subplate,
and growth-inhibiting signals from area 17 may be involved in this pro
cess.