D. Aggounzouaoui et al., GROWTH OF CALLOSAL TERMINAL ARBORS IN PRIMARY VISUAL AREAS OF THE CAT, European journal of neuroscience, 8(6), 1996, pp. 1132-1148
In kittens ranging in age between postnatal day (P) 5 and P150, callos
al axons originating near the 17/18 border were anterogradely labelled
with biocytin and reconstructed from serial sections. At the end of t
he first postnatal week most of the axons begin to invade the cortex n
ear the 17/18 border with multiple branches; some axons already span t
he grey matter up to layer I. Branches tend to grow into the grey matt
er in loose bundles less than or equal to 100 mu m in diameter, separa
ted by empty spaces of comparable width. In the following weeks additi
onal branches are produced in the grey matter; this appears to blur th
e initial bundled distribution, although by the end of the first postn
atal month the branches are distributed in discrete patches similar to
the adult terminal columns. Although a few boutons (presumably synapt
ic boutons) are found in the white matter/subplate region at earlier a
ges, they appear in the grey matter from P12 onwards. Their number per
axon increases with age, reaching adult values about the end of the f
irst month. Subsequently the number of boutons continues to increase a
nd remains above adult values at P50, P65 and P80; it then decreases,
reaching adult levels by P150. During the first month boutons tend to
be more numerous in the infragranular layers, but then the trend rever
ses in favour of the supragranular layers. In most cases, the distribu
tion of boutons spares layer IV partially or completely. From the onse
t boutons are distributed in radial 'columns' whose diameter increases
with age. They maintain selective laminar and columnar distributions
through the period of rapid and exuberant increase. These distribution
s do not appear to be sharpened further by the reduction in the number
of boutons to adult levels. On the whole, callosal terminal arbors di
fferentiate through stages of exuberant, albeit progressively constrai
ned, growth involving both progressive and regressive events. Comparis
ons with previous work suggest that visual activity might finely shape
the arbor, from the onset of synaptogenesis onwards.