Nitric oxide is a novel intercellular messenger whose role in neuronal development is not yet known. As a first step toward elucidating its developmental function, we examined the pattern of NADPH diaphorase histochemical staining, an indicator of the presence of nitric oxide synthase, in the rat spinal cord at pre and postnatal ages. Some types of neurons expressed diaphorase activity transiently during development. For example, a subset of somatic motor neurons, located in the ventrolateral corner of a few caudal segments of the cervical spinal cord, were diaphorase-positive beginning on E15, but gradually became diaphorase-negative by birth. In contrast, other spinal neurons expressed diaphorase activity continuously from development into adulthood. Preganglionic autonomic motor neurons became diaphorase-positive early in their development, as they were migrating toward their adult positions. Other spinal neurons, such as those in superficial dorsal horn, first expressed diaphorase relatively late in their development, after reaching their final location. The transient expression in some cell types, as well as the early expression in others, suggest that nitric oxide may have an important role(s) during development, which may differ from its functions in the adult nervous system.

We report here that during early fetal rat development, most, if not all, dorsal root ganglion (DRG) cells were stained by the beta-NADPH diaphorase histochemical reaction, indicating that they expressed nitric oxide synthase. During late fetal development, most DRG cells lost their diaphorase activity, but a small subset (located in all DRGs, but primarily in mid-thoracic DRGs) remained diaphorase-positive in adult animals. The transient expression of this enzyme suggests that nitric oxide may play a role during development that differs from its function in mature cells.

The displacement of immature neurons from their place of origin in the germinal epithelium toward their adult positions in the nervous system appears to involve migratory pathways or guides. While the importance of radial glial fibers in this process has long been recognized, data from recent investigations have suggested that other mechanisms might also play a role in directing the movement of young neurons. We have labeled autonomic preganglionic cells by microinjections of horseradish peroxidase (HRP) into the sympathetic chain ganglia of embryonic rats in order to study the migration and differentiation of these spinal cord neurons. Our results, in conjunction with previous observations, suggest that the migration pattern of preganglionic neurons can be divided into three distinct phases. In the first phase, the autonomic motor neurons arise in the ventral ventricular zone and migrate radially into the ventral horn of the developing spinal cord, where, together with somatic motor neurons, they form a single, primitive motor column (Phelps P. E., Barber R. P., and Vaughn J. E. (1991). J. Comp. Neurol. 307:77-86). During the second phase, the autonomic motor neurons separate from the somatic motor neurons and are displaced dorsally toward the intermediate spinal cord. When the preganglionic neurons reach the intermediolateral (IML) region, they become progressively more multipolar, and many of them undergo a change in alignment, from a dorsoventral to a mediolateral orientation. In the third phase of autonomic motor neuron development, some of these cells are displaced medially, and occupy sites between the IML and central canal. The primary and tertiary movements of the preganglionic neurons are in alignment with radial glial processes in the embryonic spinal cord, an arrangement that is consistent with a hypothesis that glial elements might guide autonomic motor neurons during these periods of development. In contrast, during the second phase, the dorsal translocation of preganglionic neurons occurs in an orientation perpendicular to radial glial fibers, indicating that glial elements are not involved in the secondary migration of these cells. The results of previous investigations have provided evidence that, in addition to glial processes, axonal pathways might provide a substrate for neuronal migration. Logically, therefore, it is possible that the secondary dorsolateral translocation of autonomic preganglionic neurons could be directed along early forming circumferential axons of spinal association interneurons, and this hypothesis is supported by the fact that such fibers are appropriately arrayed in both developmental time and space to guide this movement.

Combined [3H]thymidine autoradiographic and choline acetyltransferase (ChAT)-immunocytochemical techniques were used to answer questions concerning the generation of specific classes and subclasses of cholinergic neurons in rat brainstem. First, the generation of rostrally and caudally located neurons of the same class (i.e. somatic efferent oculomotor and hypoglossal nuclei, respectively) were compared. Results indicated that, although embryonic day 11 (E11) was the peak birthday for both nuclei, hypoglossal neurons were generated significantly earlier than oculomotor neurons, indicating a caudorostral generation gradient for brainstem somatic motor nuclei. Second, the generation patterns of 3 different subclasses of motor neurons at the same brainstem level were compared; namely those of the somatic efferent hypoglossal nucleus (XII), the general visceral efferent dorsal nucleus of the vagus (X), and the predominantly special visceral efferent nucleus ambiguus. All 3 subclasses of cholinergic cells had the same peak day (E11) and overall period of generation (E11–12). However, statistical analyses indicated a precocious generation of nucleus ambiguus, but no developmental differences between N. XII and N. X. It is suggested that nucleus ambiguus is formed earlier than N. XII and N. X, due to its more ventral location within a ventrodorsal neurogenetic gradient. Third, the generation patterns of different classes of large cholinergic neurons were examined. Specifically, the birthdays of cholinergic non-motor projection neurons of the pedunculopontine-laterodorsal tegmental nuclei (PPT-LDT) were contrasted to those of the cholinergic brainstem motor neurons. The peak birthdays of both rostrally and caudally located motor neurons were two days earlier than those of the PPT-LDT neurons. Thus, large cholinergic cells projecting to peripheral targets are born significantly earlier than those projecting within the CNS, even though the former are located more rostrally on the caudorostral neurogenetic gradient. This represents an apparent exception to the emerging rule that cholinergic neurons obey the general gradients of neurogenesis manifest in the regions of the central nervous system where they reside.

We have used a monoclonal antibody against choline acetyltransferase (ChAT) to aid in the identification of sympathetic preganglionic neurons (SPNs) and to examine their ultrastructure in rat thoracic spinal cord. The clusters of ChAT‐immumnoreactive (ChAT‐IR) preganglionic cell bodies and their distinctive bundles of dendrites give rise to a ladder‐like appearance in horizontal light microscopic sections. This organization also produced a characteristic appearance of preganglionic neuropil when viewed electron microscopically. The intermediolateral (IML) nucleus contained numerous rostrocaudally oriented ChAT‐IR dendrites extended between the IML and the central autonomic region. Both the ChAT‐IR dendrites and somata of preganglionic neurons were intimately associated with astroglial processes. The cell bodies were typically covered over a large proportion of their surfacce by a thin astrocytic sheath, and this was associated with a paucity of axon terminals forming axosomatic synapses. Instead, the vast majority of synapses upon SPNs were of the axodendritic type. The most frequently observed type of axon terminal contained numerous round, clear vesicles along with several dense‐core vesicles (DCVs). In addition, some boutons contained a predominance of DCVs. Serial section analysis revealed that these apparently diverse morphological classes of synaptic boutons may simple represent variability of structure throughout a single terminal, with a greater proportion of DCVs being located distal to the synaptic specialization and a greater number of round, clear vesicles being present adjacent to the synapse. Analysis of the dendritic bundles revealed that individual dendrites, like the cell bodies, were often isolated from each other and the surrounding neuropil by astrocytic processes. This arrangement usually was interrupted only at regions of synaptic contact where astrocytic processes surrounded the synaptic complex as a whole. Thus, astroglial ensheathment of SPNs seems designed to minimize cross‐talk between the bundled dendrites, as well as to isolate or segregate the diverse afferent inputs known to impinge on these cells.

By combining [3H] thymidine autoradiography with choline acetyltransferase (ChAT) immunocytochemistry, we have determined the generation pattern of the large cholinergic neurons in the neostriatum. All of these neurons are produced between embryonic days 12 and 17 (E12-E17), with 75% of them being born between E13 and 15. Cholinergic neurons appeared to be among the earliest cells produced in the neostriatum when compared with previous generation studies of all neurons in the rat caudate-putamen. The caudalto-rostral neurogenic gradient reported in previous investigations of all neurons was the only spatiotemporal gradient observed for cholinergic neurons. The generation peak for these cells was E13 caudally, and E15 rostrally. Additional immunocytochemical studies detected ChAT immunoreactivity within somata and primary dendrites of 1 day postnatal (1 dpn) rat neostriatum, and subsequently demonstrated a dramatic increase in the intensity of reaction product and the complexity of dendritec arborizations by 14 dpn. Large ChAT-positive neurons of the basal forebrain contained within the same specimens appeared to differentiate their cholinergic phenotype earlier than those in the neostriatum. However, recent generation studies of basal forebrain neurons combined with the present results have demonstrated that both cholinergic populations are produced simultaneously along the same neurogenic gradients. This then represents an example of cholinergic projection (basal forebrain system) and local circuit (neostriatum) neurons that share similar generation patterns but differ with respect to sequences of transmitter phenotype expression. Thus, for cholinergic forebrain neurons, a cell's position along the neurogenic gradient and its transmitter phenotype appear to be more closely associated with its birth date than its ultimate projection or rate of differentiation.

This article reviews studies of the formation of synaptic junctions in the vertebrate central nervous system. It is focused on electron microscopic investigations of synaptogenesis, although insights from other disciplines are interwoven where appropriate, as are findings from developing peripheral and invertebrate nervous systems. The first part of the review is concerned with the morphological maturation of synapses as described from both qualitative and quantitative perspectives. Next, epigenetic influences on synaptogenesis are examined, and later in the article the concept of epigenesis is integrated with that of hierarchy. It is suggested that the formation of synaptic junctions may take place as an ordered progression of epigenetically modulated events wherein each level of cellular affinity becomes subordinate to the one that follows. The ultimate determination of whether a synapse is maintained, modified or dissolved would be made by the changing molecular fabric of its junctional membranes. In closing, a hypothetical model of synaptogenesis is proposed, and an hierarchial order of events is associated with a speculative synaptogenic sequence. Key elements of this hypothesis are 1) epigenetic factors that facilitate generally appropriate interactions between neurites; 2) independent expression of surface specializations that contain sufficient information for establishing threshold recognition between interacting neurites; 3) exchange of molecular information that biases the course of subsequent junctional differentiation and ultimately results in 4) the stabilization of synaptic junctions into functional connectivity patterns.

The differentiation of dorsal root ganglion (DRG) cells with central processes in their synaptic target zones was studied in the developing spinal cord of embryonic mice (C57BL/6J). On embryonic days 12–15 (E12–E15), horseradish peroxidase (HRP) was pressure injected into the intermediate region of developing spinal grey matter and the embryos were cultured in an oxygenated medium to allow retrograde HRP transport to the dorsal root ganglia. Labelled DRG cells were measured and classified into four categories representing successive developmental stages: (1) primitive bipolar cells, (2) early transitional bipolar neurons, (3) late transitional bipolar cells, and (4) pseudounipolar neurons. In the period between E12 and E15, retrogradely labelled DRG cells became larger and less elongated as a population. Furthermore, a quantitative analysis of the cell types labelled on successive embryonic days of injection indicated an increase in the relative morphological maturity of labelled cells. On E12, the labelled cell population consisted solely of primitive bipolar and early transitional bipolar cells whereas the more mature late transitional bipolar and pseudounipolar neurons were predominant at E15, with the change between these two relationships occurring between E14 and E15. The principal finding of this study was that even the less differentiated forms of DRG neurons had axons within their central synaptic target fields during embryonic stages of spinal cord development.

The ventral striatum, previously defined as including the nucleus accumbens, substriatal grey, olfactory tubercle and striatal cell bridges has been examined in an immunocytochemical study with monoclonal antibodies to choline acetyltransferase (ChAT) in order to identify putative cholinergic neurons and synaptic junctions within the region. Light microscopy revealed ChAT-positive neurons with similar morphological characteristics in all divisions of ventral striatum. The somata of immunoreactive neurons were round or elongated in shape, approximately 10 × 21 μm in size and had two to four dendrites that coursed long distances and occasionally branched. Electron microscopy of ChAT-positive neurons in substriatal grey initially studied by light microscopy revealed that unlabelled boutons occasionally formed synapses with immunoreactive somata and proximal dendrites, but were more numerous along distal dendrites. Light microscopy demonstrated that ventral striatal neuropil contained numerous ChAT-positive fibres and punctate structures that varied in concentration from moderate to very dense. The lateral border of the substriatal grey and the area within, and adjacent to, all islands of Calleja exhibited the most dense ChAT-positive punctate staining. Additionally, the medial portion of nucleus accumbens was more densely ChAT-positive than the lateral, and the olfactory tubercle displayed laminar variations of immunoreaction product. Counterstained immunocytochemical specimens demonstrated that some areas of dense ChAT-positive punctate staining were associated with clusters of ChAT-negative, medium-sized neurons. Furthermore, electron microscopic observations of substriatal grey revealed that ChAT-positive dense regions were associated with numerous immunoreactive boutons, some of which established synapses with unlabelled somata, dendritic shafts and spines. These results suggest that the densely ChAT-positive neuropil areas within ventral striatum receive more cholinergic innervation than the more lightly stained neuropil areas. There are numerous similarities in the morphological characteristics of ChAT-positive neurons and synapses observed in ventral striatum when compared with those previously described in dorsal striatum. However, some differences were observed, such as smaller somal sizes in ventral, as contrasted with dorsal striatum, and a substantial variation in ChAT-positive fibre and punctate neuropil staining seen within the ventral but not the dorsal striatum. Such differences suggest that the ventral striatum may exhibit greater heterogeneity of cholinergic function than the dorsal striatum.

Immunocytochemical methods were used to localize the γ-aminobutyric acid (GABA) synthesizing enzyme glutamic acid decarboxylase (GAD) in normal and partially deafferented dorsal lateral vestibular nucleus (dLVN) of the rat. Normal dLVN exhibited more intense staining than the ventral part of the nucleus (vLVN), and this was mainly due to more numerous GAD + axon terminals surrounding dLVN somata and within neuropil. Small GAD + somata were also present. Electron microscopy suggested the existence of two types of GAD + synaptic terminals. The major type conformed to descriptions of Purkinje cell terminals, whereas the minor type did not. Ablation of the anterior cerebellar vermis resulted in a 73% reduction in the number of GAD + terminals, the percentage decrease being greater around neuronal somata (83%) than within neuropil (70%). The presence of GAD + somata within the nucleus and the persistence of some GAD + terminals after extensive lesions of the Purkinje cell afferents suggest that both extrinsic and intrinsic GABAergic neurons may contribute to information processing within the dLVN.

Spurious staining related to the second (linking) antibodies was observed in immunocytochemical specimens processed with an unlabeled antibody method. Some of this staining was suspected to result from species cross-reactivity of the second antibodies with endogenous immunoglobulin Gs in the tissue. Therefore, species-specific second antibodies were obtained, and the staining patterns of tissue processed with such antibodies were compared with those of tissue processed with standard (nonspecies-specific) second antibodies. In these studies, a monoclonal antibody to choline acetyltransferase (ChAT) was utilized as the primary antibody, and a similarly prepared monoclonal antibody that did not react with ChAT served as a control antibody. Spurious staining that included staining of discrete tissue and cellular components as well as amorphous background staining was present in both control and experimental tissue processed with standard second antibodies. Such staining was virtually eliminated in tissue processed with species-specific second antibodies. In specimens from the central nervous system, for example, species-specific second antibodies greatly reduced dark staining within the area postrema, in the pia-arachnoid membranes, and around blood vessels as well as the staining of small dot-like structures within some large neurons. In addition, the general level of background staining was reduced in both adult and developing tissues, thus permitting clearer visualization of many positively stained structures. In peripheral tissues such as skeletal muscle, spurious staining of connective tissue elements was eliminated, allowing the observation of previously occluded ChAT-positive structures such as nerve fibers and motor end-plates. Thus, species-specific second antibodies appear to be very useful for immunocytochemistry, particularly when the primary antibody and the tissue to be studied are from closely related species.

Glutamic acid decarboxylase (GAD), the enzyme that synthesizes the transmitter gamma-aminobutyric acid (GABA), has previously been localized within synaptic terminals in rat spinal cord by immunocytochemistry. In the present study, GAD was localized within the somata and dendrites of GABA neurons following colchicine injections into rat lumbar spinal cord. All regions of the spinal gray matter contained GAD-positive somata except the motoneuron pools (lamina IX). GAD-positive somata also were observed in the ependymal layer and in the dorsolateral funiculus. Small GAD-positive somata, averaging 9 X 13 micrometer in size, were located in laminae I-III, and the size of GAD-positive somata increased for cells located in progressively more ventral laminae, reaching a maximum in lamina VII where somal size averaged 12 X 19 micrometer. Lamina I contained two classes of GAD-positive cell bodies; lenticular shaped, intermediate size neurons that were reminiscent of stalked cells, and a smaller cell type that was elongated in the sagittal plane. GAD-positive somata in laminae II and III had the size and position of islet cells. In laminae IV-VI, GAD-positive somal profiles averaged 12 X 17 micrometer in size. Lamina IV neurons were concentrated along laminar edges, while those in laminae V and VI were distributed more homogeneously. In lamina VIII, GAD-positive cell bodies appeared in groups of 3 or 4 and were smaller than those in lamina VII. Lamina X contained GAD-positive somal profiles averaging 12 X 16 micrometer in size. In the ependymal layer, there were two types of cerebrospinal fluid (CSF)-contacting neurons that contained GAD; one spherical and the other elongated. Both types sent extensions into the central canal where these processes expanded into 4-5 micrometer-wide end bulbs. CSF-contacting cells with sizes and shapes similar to the GAD-positive ones were seen to receive synapses in electron micrographs. The widespread distribution of GABA neurons in spinal cord was suggestive of diverse functions for these cells, encompassing conventional synaptic roles and, perhaps, an involvement in hormonally modulated communication via GABAergic, CSF-contacting neurons.

Tritiated thymidine autoradiography has been used to study the generation of lateral motor neurons (LMNs), association interneurons (ANs) and dorsal root ganglion cells (DRGNs) in the spinal cords of genetically diverse strains of mice. The neuronal populations analyzed in this study form an early developing reflex pathway and the ontogeny of this circuit exhibits genetically associated variability. The strains of mice used in this investigation have been shown to differ in the embryonic age at which forelimb reflex movements are first manifest and in the timing of synapse formation within the reflex pathway. A precocious development of these reflex traits occurs in strain C57BL/6J in comparison to embryos of intermediate (CBA/CaJ) and late developing (LP/J) strains.

Antibodies prepared to purified brain glutamic acid decarboxylase (GAD), the synthesizing enzyme for the neurotrasmitter, γ-aminobutyric, acid (GABA), have been utilized with an unlabelled antibody method to localize GABAergic neurones in both light and electron microscopic preparations. A modification of Sternberger's peroxidase-antiperoxidase (PAP) complex is used to localize the site of anti-GAD binding, and the PAP complex is visualized with diaminobenzidine and H2O2. The reaction product is visible in both the light and electron microscopes. The ability to localize and identify labelled profiles in the electron microscope provides more functional information than light microscopical preparations. For example, the GAD-positive reaction product occurs mostly in association with synaptic vesicles within axon terminats, and this localization indicates the importance of GAD for the packaging and storage of GABA. The somata and dendrites of neurones giving rise to these terminals are visualized in colchicine-injected material. The GABAergic neurones form axo-somatic, axo-dendritic, axo-axonal and dendro-dendritic synapses in various regions of the rat central nervous system. Pretreatments of animals with anterograde degeneration have shown the significance of some of the GABAergic terminals that form axo-axonal synapses in the spinal cord.

Glutamic acid decarboxylase (GAD), the synthesizing enzyme for the neurotransmitter γ-aminobutyric acid (GABA), has been localized in a large number of neuronal somata within the nucleus reticularis thalami (NR) of rat brain by light microscopic immunocytochemical methods. GAD-positive staining of neuronal somata and proximal dendrites is observed in the NR of normal (untreated) rats, and this staining is substantially enhanced following colchicine injection into the lateral cerebral ventricle. GAD-positive neuronal cell bodies are prominent throughout the dorsoventral and rostrocaudal extents of the NR and, thus, form a band around the entire lateral aspect of the thalamus. In the lateral part of the NR, oval-shaped neurons with elongated GAD-positive dendritic processes are oriented parallel to the narrow axis of the NR and lie perpendicular to the penetrating fascicles of unstained thalamocortical and corticothalamic fibers. Semithin (2 μm) sections confirm that GAD-positive reaction product is containedwithin the cytoplasm of cell bodies and proximal dendrites. In addition, GAD-positive punctate structures, representing axon terminals, are present in the neuropil and, occasionally, are observed in close proximity to positively-stained neuronal somata. This finding suggests that GABA-mediated inhibition of GABA neurons may occur in the NR.

Glutamic acid decar☐ylase (GAD), the enzyme that synthesizes the neurotransmitter, GABA, was immunocytochemically localized in axon terminals as well as in small and medium-sized neurons of the rat substantia nigra. The pattern formed by GAD-containing axon terminals with the dendrites and somata of neurons in the substantia nigra was altered following ipsilateral hemitransections of the striatonigral and pallidonigral pathways. A marked reduction of GAD-positive terminals occurred throughout this brain region, but the ventral fifth of the pars reticulata showed a nearly normal pattern of GAD-positive axon terminals.

Multiple, dorsal rhizotomies were performed unilaterally at lumbar levels L1–L4 in adult rats. Following 24–48 h degeneration periods and fixation by intracardiac perfusions, spinal cord were removed and transversely cut into 150 μm thick sections. These sections were incubated in immunocytochemical reagents for the peroxidase-labeling of glutamic acid decarboxylase (GAD), the enzyme that synthesizes the neurotransmitter γ-aminobutyric acid (GABA). The sections were then prepared for electron microscopic examination, while other sections were processed for light microscopic, GAD immunocytochemistry and for Fink-Heimer staining of degenerating axons and axon terminals. Thirty-six hours following dorsal rhizotomies, the sections that were prepared for the light microscopic study of terminal degeneration showed large numbers of degenerating profiles in the ipsilateral substantia gelatinosa while degenerating profiles were virtually absent contralaterally. In electron microscopic preparations, degenerating primary afferent terminals were commonly observed at the centers of rosettes where they formed synaptic contacts with other axon terminals and with surrounding dendrites. Several types of synaptic relationships were observed in the rosettes which involved both GAD-positive and degenerating primary afferent terminals. Such synaptic relationships included those in which: (a) a single GAD-positive terminal was presynaptic to the central, primary afferent terminal, (b) two different GAD-positive terminals formed synapses with opposite sides of the same central, primary afferent terminal and were also closely apposed to the surrounding dendrites of the rosette, and (c) a GAD-positive terminal was presynaptic to a primary afferent terminal and both types of terminals were presynaptic to the same dendrite of the rosette. The synaptic relationships described in this study are discussed with respect to their possible functional roles in such GABA-mediated phenomena as: (a) primary afferent depolarization, (b) the dorsal root reflex and (c) primary afferent hyperpolarization. Our observations support the concept that GABAergic axon terminals are involved in the synaptic circuits which produce presynaptic inhibition and presynaptic facilitation of the primary afferent input to the dorsal spinal cord. Collectively the observed synaptic relationships could provide a morphological substrate that is compatible with an inhibitory surround system in the substantia gelatinosa.

Axonal growth cones and developing axonal collaterals have been studied in electron microscopic and Golgi preparations of embryonic mouse cervical spinal cord. These structures are first observed on embryonic day 11 (E11), and by E12 both axonal growth cones and developing collaterals are observed to be the presynaptic elements of developing synaptic junctions. These relatively undifferentiated portions of axons comprise nearly one-half of the presynaptic components of the synaptic contacts observed on E12, and they continue to constitute about this same proportion during the rest of the embryonic period examined (E13–16). These early synaptic interactions of developing axonal collaterals may be involved in establishing the basic ramification patterns of mature axons by determining which developing collaterals will continue to grow and differentiate.