Development of structural and functional connectivity in the thalamocortical somatosensory pathway in the wallaby.

Neuronal activity is implicated as a driving force in the development of sensory systems. In order for it to play a developmental role, however, the pathways involved must be capable of transmitting this activity. The relationship between afferent arrival, synapse formation and the onset of chemical neurotransmission has been examined using the advantageous model of a marsupial mammal, the wallaby (Macropus eugenii), to determine at what stage activity has the capacity to influence cortical development. It is known that thalamocortical afferents arrive in the somatosensory cortex on postnatal day (P)15 and that their growth cones reach to the base of the compact cell zone of the cortical plate. However, electronmicroscopy showed that thalamocortical synapses were absent at this stage. Glutamatergic responses were recorded in the cortex following stimulation of the thalamus in slices at this time but only in magnesium-free conditions. The responses were mediated entirely by N-methyl-d-aspartate (NMDA) receptors. From P28, responses could be recorded in normal magnesium and comprised a dominant NMDA-mediated component and a non-NMDA mediated component. At this time thalamocortical synapses were first identified and they were in the cortical plate. By P63 the non-NMDA-mediated component had increased relative to the NMDA-mediated component, and by P70 layer IV began to emerge and contained thalamocortical synapses. By P76 a fast non-NMDA-mediated peak dominated the response. This coincides with the appearance of cortical whisker-related patches and the onset in vivo of responses to peripheral stimulation of the whiskers.

Evidence for a visual subsector within the zona incerta.

Here we examine the patterns of connections between the zona incerta (ZI) of the thalamus and the major visual centers of the rat brain, namely the retina, dorsal lateral geniculate nucleus (LGd), superficial layers of the superior colliculus (SCs), and occipital cortex (Ocl). Injections of the tracers biotinylated dextran or cholera toxin subunit b were made into each of these centers, as well as ZI itself, by using stereotaxic coordinates. Rat brains were then aldehyde-fixed and processed using standard methods. We show that the retina, LGd, SCs, and Ocl all have connections with ZI; moreover, that each of these connections make a very distinct territory or subsector within the most lateral ZI regions. This subsector of connectivity with the visual centers does not respect the well-defined cytoarchitectonic sectors of ZI, being made up of small zones in the dorsal, ventral, and caudal sectors. Often, a distinctive "horse-shoe" pattern is evident, particularly after retinal and Ocl injections. Tracer injections into topographically distinct regions of the LGd. SCs, or Ocl results in no shift in the spatial location of labelling within ZI; after each injection, labelling is always seen within the lateral edge of the nucleus. Labelled terminals and cells are seen after LGd and SCs injections, while only labelled terminals are seen after retinal and Ocl injections. Although the precise function of this novel visual subsector is not known, these early findings suggest that ZI may be in a position to integrate visual information together with the other somatosensory, motor, and visceral information that it receives.

Disruption of retinogeniculate pattern formation by inhibition of soluble guanylyl cyclase.

During development of the visual system of the ferret, the terminals of retinal ganglion cell axons first segregate to form eye-specific layers and subsequently On-center and Off-center sublayers within the dorsal lateral geniculate nucleus (dLGN). Sublamination requires the activity of the afferent fibers, NMDA receptors, and nitric oxide synthase (NOS). We here report that soluble guanylyl cyclase (sGC), which in turn produces cGMP, is critically involved in the process of sublamination. cGMP expression is upregulated in both retinal terminals and postsynaptic dLGN cells during sublamination, and this expression is controlled by the activity of both NMDA receptors and NOS. Furthermore, the infusion of specific inhibitors of sGC or protein kinase G (PKG), a target of cGMP, prevents sublamination in vivo. We conclude that the sGC-cGMP-PKG pathway acts downstream of NMDA receptors and nitric oxide as an effector of the activity-dependent refinement of connections at this level of the mammalian visual system.

Development and plasticity of cortical areas and networks.

The development of cortical layers, areas and networks is mediated by a combination of factors that are present in the cortex and are influenced by thalamic input. Electrical activity of thalamocortical afferents has a progressive role in shaping cortex. For early thalamic innervation and patterning, the presence of activity might be sufficient; for features that develop later, such as intracortical networks that mediate emergent responses of cortex, the spatiotemporal pattern of activity often has an instructive role. Experiments that route projections from the retina to the auditory pathway alter the pattern of activity in auditory thalamocortical afferents at a very early stage and reveal the progressive influence of activity on cortical development. Thus, cortical features such as layers and thalamocortical innervation are unaffected, whereas features that develop later, such as intracortical connections, are affected significantly. Surprisingly, the behavioural role of 'rewired' cortex is also influenced profoundly, indicating the importance of patterned activity for this key aspect of cortical function.

Morphological development of afferent segregation and onset of synaptic transmission in the trigeminothalamic pathway of the wallaby (Macropus eugenii).

A light and electron microscopic study has been made of the time of formation of whisker-related patterns in trigeminothalamic afferents and the onset of synapse formation between afferents and cells in the ventroposteromedial nucleus (VPM) of the marsupial mammal, the wallaby, by labelling afferents with a carbocyanine dye. A parallel in vitro study was made of the functional development of the trigeminothalamic pathway to the VPM. Evoked synaptic responses could be recorded in the VPM from the time that afferents first reached the VPM at postnatal day 15 (P15). At all stages, the excitatory response comprised both N-methyl-D-aspartate- and non-N-methyl-D-aspartate-mediated components. At P40, the response decreased markedly in duration, coinciding with the onset of synaptogenesis. This implies that transmission is occurring prior to synapse formation, probably through transmitter release from growth cones. At P50, synaptic responses became dominated by a fast, non-N-methyl-D-aspartate potential, and this coincided with the first appearance of whisker-related patterns in the VPM. A gamma-aminobutyric acid (subtype A)-mediated, inhibitory component was also present from the time of afferent arrival. These findings support the idea that functional interactions between afferents and their targets may play a role in pattern formation in the somatosensory thalamus.

Afferent arrival and onset of functional activity in the trigeminothalamic pathway of the rat.

In this study, a novel in vitro slice preparation has been used to study the anatomical and physiological development of the trigeminothalamic pathway in the prenatal and neonatal rat. Anterograde tracing studies showed that the most rostral trigeminal fibres had reached the cephalic flexure by embryonic day (E)15, and entered the diencephalon by E16. By E17 the first few fibres had reached the ventroposteromedial thalamic nucleus (VPM) where they terminated in growth cones. The projection was more substantial and fibres had begun branching by E18, and arbors were more elaborate by E19. The fibres densely filled the nucleus by the day of birth (PO). The physiological studies showed that postsynaptic responses to stimulation of the trigeminal nerve or principal sensory nucleus (Pr5) could first be recorded at E17. Reliable responses to stimulation of either the nerve or Pr5 were recorded from E18 on. Stimulation of Pr5 enabled both axonal and synaptic signals to recorded in VPM. A GABAergic influence was acting to decrease the overall level of excitability in the thalamus from E18. In prenatal animals, the excitatory response was primarily mediated by NMDA receptors, and by P1 a non-NMDA mediated component was beginning to appear. These results demonstrate that the capacity for axonal conduction in the trigeminothalamic fibres and synaptic transmission in the thalamus are present from the time that anatomical connections are first established.

Development of whisker-related patterns in marsupials: factors controlling timing.

In mature rodents, whisker-related patterns are known to be present in three levels of the brain: the brainstem trigeminal nuclei, the ventrobasal thalamus and the somatosensory cortex. These patterns have been demonstrated using neuroanatomical tracing techniques, histological and histochemical staining methods and electrophysiological recordings. The development and topography of these patterns are dependent on an intact periphery. But what governs when patterns form at the three levels? Possibilities include a controlling signal from the periphery or local mechanisms at each site, such as the arrival of afferent inputs or the maturation of target tissue. In this review, we report on the maturation of the whisker pathway in a marsupial, the wallaby, where the slow tempo of development is a feature. At each level, afferent fibres grow into the region of termination many weeks before the whisker-related pattern emerges. The results suggest that the maturity of the target tissue as well as signals from the periphery combine to trigger pattern formation at each level of the pathway.

Nitric oxide as a signaling molecule in visual system development.

The lateral geniculate nucleus (LGN) of the ferret is characterized by the readily discernible anatomical patterning of afferent terminations from the retina into both eye-specific layers and On/Off sublaminae. The eye-specific layers form during the first post-natal week, and On/Off sublaminae become apparent during the third to fourth post-natal weeks. The post-natal appearance of these patterns thus provides an advantageous model for the study of the mechanisms of activity-dependent development. The second phase of pattern formation, the appearance of On/Off sublaminae, involves the elaboration of appropriately placed axonal terminals and the restriction (or retraction) of inappropriately placed terminals. Previous work has demonstrated that this process is dependent on the activation of NMDA-receptors. Other studies have provided strong evidence that nitric oxide, a diffusible gas which is produced downstream of NMDA-receptor activation, acts as a retrograde messenger molecule to induce changes in pre-synaptic structures. In this article we review the evidence that nitric oxide plays a role in activity-dependent synaptic plasticity in the developing retinogeniculate pathway. The role of nitric oxide in other aspects of visual system development is also discussed.

Timecourse of development of the wallaby trigeminal pathway: III. Thalamocortical and corticothalamic projections.

The development of trigeminal projections between the thalamus and cortex has been investigated in the marsupial mammal, the wallaby, by using a carbocyanine dye, horseradish peroxidase conjugated to wheat germ agglutinin (WGA-HRP), Neurobiotin, and biocytin as pathway tracers. The appearance of whisker-related patterns in the cortex in relation to their appearance in the brainstem and thalamus was examined, as was the presence or absence of a waiting period for thalamocortical afferents and the identity of the first cortical cells to project to the thalamus. Thalamic afferents first reached the cortex at postnatal day (P) 15 and were distributed up to the deep edge of the compact cell zone in the superficial cortical plate throughout development, in both dye and WGA-HRP labelled material, with no evidence of a waiting period. The initial corticothalamic projection, detected by retrograde transport of WGA-HRP from the thalamus, occurred at P60 from layer 5 cells. This was confirmed by labelling of corticothalamic axons after cortical injections of Neurobiotin and biocytin. Scattered, labelled cells seen before P60 after dye labelling from the thalamus presumably resulted from transcellular labelling via thalamic afferents. Clustering of afferents in layer 4 and cell bodies and their dendrites in layers 5 and 6 first occurred simultaneously at P76. There is a sequential onset of pattern formation, first in brainstem, then in thalamus, and finally in cortex, with a long delay between afferent arrival and pattern formation at each level. Independent regulation at each level, likely depending on target maturation, is suggested.

Timecourse of development of the wallaby trigeminal pathway. II. Brainstem to thalamus and the emergence of cellular aggregations.

This paper is the second in a series which makes use of the protracted postnatal maturation of the wallaby to study the development of the trigeminal sensory system. Previous work has established similarities in the organisation of the trigeminal sensory system in the wallaby and in rodents. This study describes the structure and development of the ventroposteromedial nucleus in the wallaby in relationship to the arrival of afferents from the trigeminal nuclei, the formation of neuronal aggregations and naturally occurring cell death. Enzyme histochemistry, Nissl and myelin stains were used. Pathway development was followed using carbocyanine dyes. In the adult wallaby the nucleus demonstrates evidence of a parcellated organisation. Cells are arranged in dorsoventrally aligned bands resembling fingers. In the horizontal plane, these appear as circular clusters which are encircled by fine myelinated bundles. The clusters of cells are believed to correspond to the mystacial vibrissae. The first afferents from the principal trigeminal nucleus arrive between 10 and 15 days postnatal. This is more than two weeks prior to the time at which the borders of the nucleus can be discerned cytoarchitecturally. The first hints of segmentation are visible around day 50, and discrete aggregations form over the ensuing 3-4 weeks. Coincident with the aggregation of the neurons is an increase in their level of reactivity for acetylcholinesterase. A high level of acetylcholinesterase reactivity is maintained for at least 4 months, but has disappeared in adult animals. The peak of cell death occurs subsequent to the appearance of aggregations in the thalamus, but coincident with the appearance of vibrissae related patches in the cortex at day 85 (Waite et al. [1991] Dev. Brain Res. 58:35-41). The timing of the appearance of the neuronal aggregations supports the hypothesis that pattern formation occurs sequentially at successive levels of the pathway, and suggests the importance of target maturation in pattern formation.

Timecourse of development of the wallaby trigeminal pathway. I. Periphery to brainstem.

The development of the vibrissae and their innervation and the maturation of the brainstem trigeminal sensory nuclei have been studied in the wallaby, Macropus eugenii, from birth to adulthood. At birth, developing vibrissal follicles consist of solid epidermal pegs surrounded by dermal condensations. The developing follicles and adjacent skin are innervated by trigeminal afferents. Ten days after birth the follicle contains a dermal papilla and the deep vibrissal nerve can be recognised. A hair cone is present at postnatal day (P) 30 and hairs are apparent on the skin surface by P35. By P63 the deep vibrissal nerve can be seen innervating Merkel cells in the outer root sheath; in addition, the first signs of the blood sinus can be recognised. Innervation of the inner conical body and lanceolate and lamellated receptors supplying the mesenchymal sheath and waist region are not seen until P119, when the follicle resembles that seen in the adult. At birth, central processes of the trigeminal ganglion cells have entered the trigeminal tract and extend from the rostral pons to the upper cervical cord. Labelling with a carbocyanine dye at P0 shows afferents extending medially from the tract into the trigeminal subnuclei at all levels. At this stage the trigeminal nuclei appear as areas of increased cell density in the lateral brainstem. By P30-40 the four subnuclei can be distinguished on the basis of shape, cytoarchitecture, and succinic dehydrogenase reactivity. Adult morphology is not fully established until P210. In mature animals, nucleus principalis contains closely packed, polymorphic cells, frequently aligned parallel to thick fibre bundles that traverse the nucleus obliquely. Subnuclei oralis and interpolaris contain sparsely distributed, medium to large cells, randomly oriented, as well as prominent rostrocaudally directed fibre bundles. Subnucleus caudalis consists of the marginal layer, substantia gelatinosa, and magnocellular layers as described in other species. Patches of increased succinic dehydrogenase or cytochrome oxidase reactivity, presumably corresponding to the vibrissae, are present in subnuclei principalis, interpolaris, and caudalis in developing and adult animals, although the pattern is less clear than in rats. The brainstem patches are first seen at P40, approximately 6 weeks before the corresponding vibrissal-related pattern develops in the cortex. This suggests that the onset of patch formation may be regulated independently at different levels of the pathway.