Onset of synaptogenesis in the plexiform layers of the chick retina: a transmission electron microscopic study.

The presently acknowledged onset of synaptogenesis in the chick retina from embryonic day 12 (E12) onward stands in contrast with the appearance of spontaneous electrical activity, of presynaptic proteins, or of neurotransmitters during early formation of the inner (E6-E8) and outer (E9) plexiform layers. Therefore, we investigated the chick retina from E6 to E12 at which age first synapses appear by transmission electron microscopy (TEM). The study provides evidence that synaptogenesis in the chick retina begins shortly after the plexiform layers have started to emerge. The first synapses are electrical synapses, which appear on E7, one day after the future inner plexiform layer emerged, and towards the end of E8 in the nascent outer plexiform layer. Conventional chemical synapses appear in both plexiform layers on E8, in the inner plexiform layer (stage 34) only a few hours earlier than in the outer plexiform layer (stage 35). The first synapses are formed close to the apex of the optic fissure and their frequency increases rapidly with age. The onset, the topography, and the developmental course of synaptogenesis correlate with the chronotopic course of maturation of retinal neurons and the age when spontaneous electrical activity occurs in the retina.

On the postnatal development of the striate cortex (V1) in the tree shrew (Tupaia belangeri).

Histological serial sections, three-dimensional reconstructions and morphometry served to study the postnatal development of V1 in tree shrews. The main objectives were to evaluate the expansion of V1, the implications of its growth on the occipital cortex and, vice versa, the effects of the expanding neocortex on the topography of V1. The future V1 was identified on postnatal day 1 by its granular layer IV, covering the superior surface of the occipital cortices including the poles. A subdivision of layer IV, distinctive for the binocular part, was evident in the central region. V1 expanded continuously with age into all directions succeeded by the maturation of layering. The monocular part was recognized from day 15 onward, after the binocular part had reached its medial border. In reference to the retinotopic map of V1, regions emerged in a coherent temporo-spatial sequence delineating the retinal topography in a central to peripheral gradient beginning with the visual streak representation. The growth of V1 was greatest until tree shrews open their eyes, culminated during adolescence, and completed after a subsequent decrease in the young adult. Simultaneous expansion of the neocortex induced a shifting of V1. Translation and elongation of V1 entailed that the occipital cortex covered the superior colliculi along with a downward rotation of the poles. The enlargement of the occipital part of the hemispheres was in addition associated with the formation of a small occipital horn in the lateral ventricles, indicating an incipient 'true' occipital lobe harbouring mainly cortices involved in visual functions.

On the development of the stratification of the inner plexiform layer in the chick retina.

This study investigated the development of the subdivision of the chick inner plexiform layer (IPL). The approach included an immunohistological analysis of the temporal and spatial expressions of choline acetyltransferase, of the neural-glial-related and neural-glial cell adhesion molecules (NrCAM and NgCAM, respectively) and axonin-1, and of inwardly rectifying potassium (Kir) channels in 5- to 19-day-old (E5-E19) embryos. Ultrastructural investigations evaluated whether synaptogenesis accompanies the onset of differentiation of the IPL. We found that the differentiation of the IPL started at E9. Distinct cholinergic strata appeared, NrCAM immunoreactivity showed a poorly defined stratification, and Kir3.2 was expressed in the IPL and in the inner nuclear layer. From E10 until late E14, NgCAM- and axonin-1-immunoreactive strata emerged in an alternating sequence from the outer to the inner IPL. During this period, the NrCAM pattern sharpened, and eventually five bands of weaker and stronger immunoreactivity were found. Conventional synapses formed at the beginning of E9, and stratification of the IPL also began on the same day at the same location. Synaptogenesis and stratification followed a gradient from the central to the peripheral retina. The topographic course of differentiation of the IPL generally corresponded to the course of maturation of ganglion and amacrine cells. Synaptogenesis and the expression of G-protein-gated Kir3.2 channels accompanied the onset of stratification. These events coincide with the occurrence of robust and rhythmic spontaneous neuronal activity. The subsequent differentiation of the IPL seemed to be orchestrated by several mechanisms.