The fine structure of the inferior colliculus in the cat. II. Synaptic organization.

The synaptic organization of the central nucleus of the inferior colliculus (ICc) of the cat has been investigated by means of electron microscopy. On the basis of the following criteria: the size and the shape of the synaptic vesicles, the distribution and density of the vesicular population, the size and the shape of the synaptic boutons, their origin, and the characteristics of the active synaptic zones, several types of synaptic boutons in the ICc have been discriminated: LR1, LR2, SR, SSB, F1, F2, P, DCV-terminals, and "d"-profiles. The LR1, LR2, SR and SSB bouton types contain clear, round or slightly oval synaptic vesicles and form asymmetrical synapses mainly with middle sized and small dendrites and dendritic spines. LR2-terminals not rarely contact also the neuronal perikarya, whilst the SR-boutons form exclusively axodendritic and axospinous synapses. The P, F1 and F2-boutons contain a pleomorphic vesicular population (P-boutons), with an increased degree of vesicle flattening (F1 and F2-boutons) and form symmetrical axosomatic, axodendritic and axospinous contacts. Especially often the F1-boutons form axosomatic synapses, whilst the F2-terminals end mainly on dendrites. The DCV-boutons contain a mixed population of clear round synaptic vesicles and large dense core vesicles. The DCV-boutons terminate mainly on spines and small distal dendrites by means of asymmetrical synaptic specializations. The "d"-profiles originate from dendrites, and are identical to the thalamic "d"-profiles but are far more rarely observed in the ICc. The "d"-profiles are postsynaptic mainly to the LR-types, and are presynaptic to conventional dendrites, thus participating in synaptic triads. The axonal hillocks and the initial axonal segments of the larger perikarya in the ICc are substantially innervated mainly by LR and P-boutons. Glomerulus-like formations are fairly often, especially around the LR1-terminals, contacting several small postsynaptic targets. True synaptic glomeruli are only rarely observed. Branching myelinated axons are found mainly within the fibrodendritic laminae, whilst unmyelinated collaterals, emitted by myelinated axons are especially often encountered outside the laminae. Various types of myelinated axons form nodal synapses.     

Distribution of the piriform cortical terminals to cells in the central segment of the mediodorsal thalamic nucleus of the rat.

A Golgi electron microscopic study was undertaken to investigate the distribution of terminals from the piriform cortex that synapse on identified dendrites of neurons in the central segment of the mediodorsal thalamic nucleus of the rat. The piriform cortical terminals were identified as degenerating terminals following lesions in the cortex. They consisted of two types, i.e., large (LR type) and small (SR type) presynaptic terminals, both of which had round synaptic vesicles and formed asymmetric synaptic contacts. SR boutons terminated preferentially onto distal dendrites and never synapsed on primary dendrites. LR terminals synapsed preferentially on proximal dendrites, but were also found on more distal dendritic segments.     

Parvalbumin-immunoreactive neurons in the rat neostriatum: a light and electron microscopic study

Parvalbumin (PV)-immunoreactive neurons in rat neostriatum were studied under light and electron microscopes. A small number of neurons in the striatum were immunoreactive for PV (a Ca-binding protein). Most of them were also strongly immunoreactive for glutamate decarboxylase but were negative for NADPH-diaphorase activity. Light microscopic analysis revealed that PV-containing neurons have somata with fusiform or polygonal shape and are medium to large in size. The dendrites were smooth and cylindrical at the proximal portion but were varicose at the distal portion. Thin PV-immunoreactive fibers with large boutons were unevenly distributed in the striatum. Electron microscopy revealed that the somata of PV-immunoreactive neurons had a deeply indented nucleus with a nucleolus and often an intranuclear rod. These are the morphological features reported for interneurons of the striatum. Gap junctions formed between two neighboring PV-immunoreactive dendrites. A total of 175 boutons forming synapses with somata and dendrites of PV-immunoreactive neurons were examined. Of these, 115 were small in diameter (less than 1 micron), contained densely packed round vesicles and formed asymmetrical synapses mainly with dendrites. The other 60 boutons formed symmetrical synapses with somata and dendrites of PV-immunoreactive neurons. Both myelinated and unmyelinated axons with boutons were observed. PV-immunoreactive boutons had a diameter of 0.3-2 microns and contained round or elongated vesicles which were about 35 nm in diameter. The boutons formed symmetrical synapses with postsynaptic targets. Of the 100 PV-immunoreactive boutons, 51 were found on somata and proximal dendrites of medium-sized neurons containing a large, round, centrally located nucleus. The others formed synapses with dendrites of various sizes. It was occasionally observed that varicose dendrites free of spines were contacted by a large number of PV-immunoreactive boutons. The study indicates that, in the striatum, immunocytochemistry for PV selectively stains GABAergic interneurons and that the GABAergic interneurons are incorporated in a feed-forward inhibitory circuit of the striatum.     

Distribution patterns of individual medial lemniscal axons in the ventrobasal complex of the monkey thalamus

Somatostatin-immunoreactive neurons in the rat neostriatum were studied by correlated light and electron microscopy using the peroxidase-antiperoxidase immunocytochemical technique. Immunoreactivity was localized in neuronal perikarya and processes. The perikarya were of spindle or fusiform shape (average length 16.9 microns) and were found in all parts of the neostriatum. From each neuron there arose two to four straight immunoreactive dendritelike processes, which could frequently be traced as far as about 130 microns from their perikaryon. Immunoreactive varicose axonlike processes were occasionally found, some of which were proximal axons of identified immunoreactive cells. Nine of the light microscopically identified neurons showing somatostatin-immunoreactivity were studied in the electron microscope; two of them had proximal axons with varicosities. Each neuron had an oval or elongated nucleus, which was always indented. These morphological features correspond well to those of certain "medium-size aspiny" neurons classified by Golgi studies. Although the immunoreactive endproduct was diffusely located throughout the neuron, it was characteristically located in the saccules and large granules (diameter 133 nm) of the Golgi apparatus, and large immunoreactive vesicles of similar size to those in the Golgi apparatus frequently occurred in all parts of axon. Very little synaptic input was found on the perikarya and dendrites of somatostatin-immunoreactive neurons. The perikarya and proximal dendrites received both symmetrical and asymmetrical synaptic input, while the distal dendrites usually received boutons that formed asymmetrical contacts. The somatostatin-immunoreactive boutons contained pleomorphic electron-lucent vesicles (diameter 39.3 nm) and a few large immunoreactive granular vesicles; these boutons always formed symmetrical synapses. Their postsynaptic targets were dendritic shafts, spines, and unclassified dendritic profiles. On the other hand, the varicosities of identified proximal axons of somatostatin-positive neurons did not form typical synapses, since they lacked clusters of small vesicles, but some of them were in direct apposition (via membrane specializations) to unlabelled perikarya or dendrites. It is concluded that somatostatin is a useful marker for a particular type of neuron in the neostriatum. The presence of somatostatin immunoreactivity in synaptic boutons is consistent with the view that somatostatin could be a neurotransmitter in the neostriatum.     

Immunocytochemical localization of choline acetyltransferase within the rat neostriatum: a correlated light and electron microscopic study of cholinergic neurons and synapses

Monoclonal antibodies to choline acetyltransferase (ChAT) were used in an immunocytochemical study to characterize putative cholinergic neurons and synaptic junctions in rat caudate-putamen. Light microscopy (LM) revealed that ChAT-positive neurons are distributed throughout the striatum. These cells have large oval or multipolar somata, and exhibit three to four primary dendrites that branch and extend long distances. Quantitative analysis of counterstained preparations indicated that ChAT-positive neurons constitute 1.7% of the total neuronal population. Electron microscopy (EM) of immunoreactive neurons initially studied by LM revealed somata characterized by deeply invaginated nuclei and by abundant amounts of organelle-rich cytoplasm. Surfaces of ChAT-positive neurons are frequently smooth, but occasional somatic protrusions and dendritic spines occur. Although infrequently observed, axons of ChAT-positive neurons branch, receive synapses, and become myelinated. Unlabeled boutons make both symmetrical and asymmetrical synapses with ChAT-positive somata and proximal dendrites, but are more numerous on distal dendrites. In addition, some unlabeled terminals form asymmetrical synapses with ChAT-positive somata and dendrites that are distinguished by prominent subsynaptic dense bodies. Light microscopy demonstrated a dense distribution of ChAT-positive fibers and punctate structures in the striatum, and these structures appear to correlate, respectively, with labeled preterminal axons and presynaptic boutons identified by EM. ChAT-positive boutons contain pleomorphic vesicles, and make symmetrical synapses primarily with unlabeled dendritic shafts. Furthermore, they establish synaptic contacts with somata, dendrites and axon initial segments of unlabeled neurons that ultrastructurally resemble medium spiny neurons. These observations, together with the results of other investigations, suggest that medium spiny GABAergic projection neurons receive a cholinergic innervation that is probably derived from ChAT-positive striatal cells. The results of this study also indicate that cholinergic neurons within caudate-putamen belong to a single population of cells that have large somata and extensive sparsely spined dendrites. Such neurons, in combination with dense concentrations of ChAT-positive fibers and terminals, are the likely basis for the large amounts of ChAT and acetylcholine detected biochemically within the neostriatum.     

The structural organization of the inferior and lateral subdivisions of the Macaca monkey pulvinar.

Previous light microscopic studies of Macaca pulvinar have demonstrated that both the inferior and adjacent portion of the lateral pulvinar subdivisions are reciprocally connected to the entire occipital lobe, including striate cortex. They differ in that inferior but not lateral pulvinar receives a projection from the superficial layers of the superior colliculus. In this study, the internal organization of these two subdivisions in compared by relating light microscopic Golgi morphology to the synaptic organization observed by electron microscopy. The Golgi impregnated neurons in inferior and lateral pulvinar are typical of other thalamic nuclei and are not qualitatively different in the two subdivisions. Projections neurons (PN) vary in cell body (15--40 micrometers) and dendritic tree (150--600 micrometers) diameters but bear the same varieties of dendritic appendages; spine-like, hair-like, and knot-like. Local circuit neurons (LCN) have smaller cell body diameters (10--20 micrometers) but can have very large dendritic field diameters (150--600 micrometers). They are best distinguished from PNs by their elaborate dendritic appendages, which have been identified as pre-synaptic dendrites in the EM. LCN axons are infrequently seen. In the EM both subdivisions contain four types of synaptic terminals. RS and RL terminal both contain round symaptic vesicles and make asymmetric synaptic contacts, but are subdivided on the basis of small (RS = 0.09 micrometers) versus large (RL = 2.2 micrometers) cross sectional diameters and organelle content. RLs contact larger caliber dendrites and frequently form synaptic complexes with presynaptic dendrites of LCNs, while RSs contact fine caliber dendrites and rarely take part in synaptic complexes. F terminal and P boutons both contain flat and pleomorphis vesicles and make symmetric synaptic contacts. They are characterized by vesicle number and cytoplasmic density. Fs are infrequently observed in pulvinar compared to P boutons and are of uncertain origin. P boutons can be equated with LCN dendritic appendages and have been identified as pre-synaptic dendrites. The quantitative distribution of each type is very similar in both subdivisions, avveraging RS 85%, RL 5%, F 0.3%, P 8% and unidentified 2%.     

The fine structure of the subthalamic nucleus in the cat. II. Synaptic organization. Comparisons with the synaptology and afferent connections of the pallidal complex and the substantia nigra

The synaptic organization of the subthalamic nucleus (Sth) of the cat has been investigated by means of electron microscopy. On the basis of the following criteria: the size and the shape of the synaptic boutons, their origin, the size and the shape of the synaptic vesicles, the distribution and density of the vesicular population, and the characteristics of the active synaptic zones, several types of synaptic boutons have been discriminated: F1, F2, SR, LR1, LR2, d.c.v., and "d" profiles. The F1 and F2 types have pleomorphic vesicles and form symmetrical synapses with the neuronal perikarya, the proximal dendrites and their spines, as well as with the initial axonal segments. The SR, LR1 and LR2 types contain round or oval vesicles and form asymmetrical synapses mainly with middle sized and small dendrites, and their spines. The d.c.v. boutons contain a mixed population of clear synaptic vesicles and dense core vesicles. The d.c.v. type forms asymmetrical synapses. The "d" profiles share identical features with the vesicle containing dendrites. The F2, SR, LR1, LR2, and "d" profiles take part in synaptic diads and/or triads, and occasionally participate in the synaptic glomeruli. The LR1 and LR2 take part in glomeruluslike formations. The Sth has a distinct synaptic pattern that permits its discrimination as a separate ultrastructural entity. The Sth seems to share some common ultrastructural features with the thalamic nuclei. On the other hand, the ultrastructural aspects of the Sth are much more different from its closest embryological allies: the both pallidal segments, and the zona reticulata of the substantia nigra.     

Cartwheel neurons of the dorsal cochlear nucleus: a Golgi-electron microscopic study in rat

Cartwheel neurons in rat dorsal cochlear nucleus (DCN) were studied by Golgi impregnation-electron microscopy. Usually situated in layers 1-2, cartwheel neurons (10-14 micrometers in mean cell body diameter) have dendritic trees predominantly in layer 1. The dendrites branch at wide angles. Most primary dendrites are short, nontapering, and bear only a few sessile spines. Secondary and tertiary dendrites are short, curved, and spine-laden. The perikaryon forms symmetric synapses with at least two kinds of boutons containing pleomorphic vesicles. The euchromatic nucleus is indented and has an eccentric nucleolus. The cytoplasm shows several small Nissl bodies, a conspicuous Golgi apparatus, and numerous subsurface and cytoplasmic cisterns of endoplasmic reticulum with a narrow lumen, joined by mitochondria in single or multiple assemblies. In primary dendrites mitochondria are situated peripherally, while in distal branches they become ubiquitous and relatively more numerous. Dendritic shafts usually form symmetric synapses with boutons that contain pleomorphic vesicles. The majority of the dendritic spines are provided with a vesiculo-saccular spine apparatus. All dendritic spines have asymmetric synapses. Most of these are formed with varicosities of thin, unmyelinated fibers (presumably axons of granule cells) running parallel to the long axis of the DCN or radially. These varicosities contain round, clear synaptic vesicles. On the initial axon segment few symmetric synapses are present. The axon acquires a thin myelin sheath after a short trajectory. Cartwheel neurons outnumber all other neurons in layers 1-2 (with the exception of granule cells), and presumably correspond to type C cells with thinly myelinated axons described by Lorente de Nó. The axons of these neurons provide a dense plexus in the superficial layers without leaving the DCN. The possible functional role of cartwheel neurons is discussed.     

Synaptic organization of projections from basal forebrain structures to the mediodorsal thalamic nucleus of the rat.

The synaptic organization of the mediodorsal thalamic nucleus (MD) in the rat was studied with the electron microscope, and correlated with the termination of afferent fibers labeled with wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP). Presynaptic axon terminals were classified into four categories in MD on the basis of the size, synaptic vesicle morphology, and synaptic membrane specializations: 1) small axon terminals with round synaptic vesicles (SR), which made asymmetrical synaptic contacts predominantly with small dendritic shafts; 2) large axon terminals with round vesicles (LR), which established asymmetrical synaptic junctions mainly with large dendritic shafts; 3) small to medium axon terminals with pleomorphic vesicles (SMP), which formed symmetrical synaptic contacts with somata and small-diameter dendrites; 4) large axon terminals with pleomorphic vesicles (LP), which made symmetrical synaptic contacts with large dendritic shafts. Synaptic glomeruli were also identified in MD that contained either LR or LP terminals as the central presynaptic components. No presynaptic dendrites were identified. In order to identify terminals arising from different sources, injections of WGA-HRP were made into cortical and subcortical structures known to project to MD, including the prefrontal cortex, piriform cortex, amygdala, ventral pallidum and thalamic reticular nucleus. Axons from the amygdala formed LR terminals, while those from the prefrontal and insular cortex ended exclusively in SR terminals. Fibers labeled from the piriform cortex formed both LR and SR endings. Based on their morphology, all of these are presumed to be excitatory. In contrast, the axons from the ventral pallidum ended as LP terminals, and those from the thalamic reticular nucleus formed SMP terminals. Both are presumed to be inhibitory. At least some terminals from these sources have also been identified as GABAergic, based on double labeling with anterogradely transported WGA-HRP and glutamic acid decarboxylase (GAD) immunocytochemistry.     

GABAergic elements in the neuronal circuits of the monkey neostriatum: a light and electron microscopic immunocytochemical study

An antibody raised in rabbits against a GABA-BSA conjugate was used together with the PAP technique to label elements in the neostriatum of three Old World monkeys. Light microscopy revealed numerous immunoreactive medium-size neurons of various staining intensities, some of which had indented nuclei, as well as an occasional large cell. The neuropil showed a plexus of fine processes with frequent puncta. Ultrastructurally, the medium-size GABA-positive neurons were of two types: one with smooth nuclei and scanty cytoplasm, similar to spiny I cells, the other with invaginated nuclear envelopes and more abundant perikaryon, resembling the aspiny type. Correspondingly, labeled dendrites were either spiny or varicose. Some stained axons were myelinated, and the boutons had either large and ovoid, or small and pleomorphic vesicles. All of these boutons formed symmetric synapses, the former type with GABA-positive dendritic shafts but also with unlabeled dendrites; the latter type usually with GABA-negative elements, either dendrites, dendritic spines, or somata. Synapses were also observed between unreactive boutons and immunostained dendrites. Terminals with densely packed, small round vesicles that established asymmetric synapses with spines were always GABA-negative. Glial elements were consistently unlabeled, save for some astroglial endfeet. These findings provide positive evidence for the existence of two classes of GABAergic striatal neurons corresponding to a long-axoned spiny I type and an aspiny interneuron. Furthermore, the simultaneous labeling of GABA-immunoreactive presynaptic and postsynaptic profiles offers possible morphologic bases for the various kinds of intrastriatal inhibitory processes, including the feedforward, feedback, and "autaptic" types.     

An EM-autoradiographic analysis of the projection from cortical areas 17, 18, and 19 to the superior colliculus in the cat

The electron microscopic autoradiographic method was used to identify terminals of axons from cortical areas 17, 18, and 19 in the superficial layers of the superior colliculus. The results show that terminals of area 17 neurons contain round vesicles and made asymmetrical synaptic contacts predominantly onto one or more dendrites or dendritic appendages. Some profiles postsynaptic to labeled terminals contain vesicles and presumably are involved in serial synaptic arrangements. Terminals of area 18 and 19 neurons in the superficial collicular layers appear to comprise two populations, one similar in most respects to area 17 terminals, containing round vesicles and making asymmetrical contacts. The other contains pleomorphic vesicles and makes symmetrical contacts upon dendrites and dendritic appendages. These terminals rarely contact more than one postsynaptic profile, and rarely do the postsynaptic profiles contain vesicles. The two populations of area 18 and 19 terminals containing round and pleomorphic vesicles, respectively, are present in the ratio of approximately 3:1, although this ratio varies throughout the sublaminae of the superficial collicular layers. The presence of two distinct types of cortical terminals in the colliculus suggests that cortical modulation of collicular processing is more complex than was previously conceived.     

Neuronal and synaptic composition of the mediodorsal thalamic nucleus in the rat: a light and electron microscopic Golgi study.

The distribution and dendritic domain of neurons in each segment of the mediodorsal thalamic nucleus (MD) have been studied in the rat with the Golgi technique. In addition, a combined Golgi method-electron microscopic (Golgi-EM) study was undertaken to determine the distribution of morphologically distinct synapse types along the dendrites of individual identified neurons in MD. All the subdivisions or "segments" of MD (medial, central, lateral) contained both stellate and fusiform cells. The dendritic domain of both types of cells was predominantly restricted to the same segment of MD that contained the cell body of the neuron. Typical stellate neurons were found near the center of each segment, with radiating dendrites that extended to but not across the boundaries of the segment. Fusiform cells were usually located close to the segmental or nuclear boundaries and tended to have dendrites oriented parallel to those borders; again, the dendrites tended not to extend across borders between segments or at the outer edge of MD. In the medial segment of MD many fusiform cells had especially bipolar dendritic configurations, generally with a dorsoventral orientation. Because no small neurons were identified that might correspond to thalamic interneurons, all the impregnated cells in MD are presumed to be thalamocortical projection neurons. These results indicate that cells and their major dendrites are confined to a single segment of MD, with little dendritic overlap across segmental or nuclear borders. The segments of MD may therefore be considered to be relatively independent subnuclei. The distribution of the four types of synapses previously identified in MD (Kuroda and Price, J. Comp. Neurol., 303:513-533, 1991) was determined along several identified dendrites studied with the Golgi-EM method. Primary dendrites were contacted mostly by large axon terminals, including both large, round vesicle (LR) terminals and large, pleomorphic vesicle (LP) terminals, as well as a few small to medium sized terminals with pleomorphic vesicles (SMP). No small terminals with round vesicles (SR terminals) were observed to make synapses with primary dendrites. Secondary and tertiary dendrites received synapses from all types of axon terminals. Higher order dendrites were contracted predominantly by SR boutons, but they also carried some LR and SMP terminals. In addition, SMP boutons were often found to form symmetric contacts with cell somata.     

Corticotectal terminals in the superior colliculus of the rabbit: a light- and electron microscopic analysis using horseradish peroxidase (HRP)-tetramethylbenzidine (TMB)

The projection from the striate cortex to the superior colliculus was studied light- and electron microscopically by means of anterogradely transported horseradish peroxidase and tetramethylbenzidine histochemistry. Labeled boutons were found in the stratum zonale (SZ) and in the stratum griseum superficiale (SGS), not in stratum opticum (SO). There are two maxima of frequency of labeled boutons, one in middle SGS at about 500 microns depth, and a smaller one in upper SGS at about 200 microns depth. Such a bimodal distribution of corticotectal terminals has not been described in any species before. Labeled myelinated axons were found in SGS and SO with a maximal frequency in middle SGS at about 400 microns depth. The myelinated axons in SZ, which are commonly considered to be of cortical origin, were not labeled. The labeled cortical terminals contained numerous round synaptic vesicles and predominantly dark mitochondria. They formed usually asymmetrical synapses and contacted dendrites, some of which contained synaptic vesicles. Occasionally, labeled boutons were observed which definitely did not belong to the type that is generally considered to be of cortical origin.     

Ultrastructure of supraspinal dorsal root projections in the toads. I. The obex region

The ultrastructure of the dorsal column nucleus (DCN) has been investigated at the level of the obex region in normal and experimental toads. Large 'isolated' neurons (greater than 20 micrometer) and clusters of small neurons (less than 20 micrometer) have been identified in this region. Synaptic profiles have been classified into three types: large 'en passant' LR boutons, containing round synaptic vesicles and neurofilaments, small R boutons with round vesicles and F boutons with pleomorphic vesicles. The axon terminals exhibited synaptic contacts with cell somata, with dendrites of varying calibers and with other axons. The terminals involved in the axo-axonic contact were the F boutons which were presynaptic to the LR boutons, thus representing the morphological basis for presynaptic inhibition. Transection of the second dorsal root was performed in order to identify the terminals of the primary afferents to the DCN, after different survival periods (16 h--50 days). Only the LR boutons underwent degeneration, thus representing the central endings of the primary dorsal root afferents. The functional significance of these findings was discussed.     

The cytoarchitecture and some efferent projections of the centromedian-parafascicular complex in the lesser bushbaby (Galago senegalensis)

The morphology of neurons in the centromedian (CM) and parafascicular (PF) nuclei in the lesser bushbaby (Galago senegalensis) is described in coronal and horizontal brain sections using Golgi-, horseradish peroxidase (HRP)-, and Nissl-staining procedures. The CM contains two types of cells referred to as principal neurons and Golgi type II (like) neurons. Cell bodies of principal neurons are relatively large in cross-sectional area (mean = 130.42 micron2), round to spindle in shape, support short somatic spines, and give rise to three to five primary dendrites. The dendrites branch in a "radiate" pattern and possess numerous appendages consisting of narrow, stalk-supported swellings. The presumed axons of these cells are impregnated only in their initial segments. On the basis of the similarity of principal neuron soma shapes and cross-sectional areas with those of HRP-reactive somata following cortical HRP implantation, it is concluded that at least some of the principal neurons in Galago CM project to somatic sensory-motor cortex. Golgi type II (like) neurons have small (mean = 79.43 micron2), round somata which support several spines and give rise to three to four small-diameter dendrites. The dendrites are infrequently branched, sinuous in their courses, and give rise to complex appendages and beaded processes. However, the axons of these cells could not be seen to ramify in the immediate vicinity of the dendritic field or soma, and there is considerable overlap in the cross-sectional areas of Golgi type II (like) neurons seen in Golgi preparations and HRP-stained cells following cortical implant of HRP pellets. Consequently, although Golgi type II (like) cells have traits characteristic of classically described intrinsic neurons, a cortical projection of these cells cannot be ruled out by the present study. The parafascicular nucleus contains two groups of large, radiate cells characterized by the presence or absence of somatic spines. Cells with somatic spines also contain numerous appendages on the dendrites. Cells without somatic spines support only a few, isolated, short dendritic appendages. Numerous small cell-bodied neurons are present in Nissl-stained sections of PF; however, cells which resemble Golgi type II neurons were not observed in the PF in the present Golgi-impregnated material. In contrast to the CM, the large cell-bodied neurons in PF were not found to project to somatic sensory-motor cortex in Galago.     

The structure of the dorsal lateral geniculate nucleus in the mouse. A Golgi and electron microscopic study

Two types of neurons have been distinguished in Golgi and electron microscopic preparations of the dorsal lateral geniculate nucleus of young mice. In addition to a thalamo-striate relay cell (TSR neuron) with brush-like dendritic arbors and a thick, unbranched axon, a small tomedium size cell (PA neuron) of oval or spindle shaped body and few, long and seldom branched dendrites is frequently identified in our Golgi preparations. This second type of cell may exhibit none, one or several sparsely branched axon-like processes which terminate in the vicinity of the cell body. The dendrites of the PA neurons show characteristically large, spheroidal processes (p) 1–3 m? in diameter issuing forth singly, in clusters or as a “string of beads” from delicate, often long, pedicles attached to the dendritic shafts. Profiles comparable to these processes and in apparent continuity with PA dendrites have been identified with the electron microscope and show synaptic vesicles and a system of sacs of smooth E.R. The portions of the dendrites from which these vesicle-containing processes issue also show clusters of vesicles, ribosomes and an orderly array of microtubules. Golgi impregnated axons are followed from the optic tract and seen terminating as irregular enlargements (2–6 m?) on proximal dendrites of relay cells and on distal dendrites of the PA neuron. The intimate contact of the terminal branches of an optic collateral with a distal PA dendrite is carefully illustrated. Small calibered axons are likewise traced from the internal medullary lamina and seen to end by means of end-knobs on distal dendrites of both types of neurons. Electron microscopic observations substantiate the Golgi images and reveal three different types (I, II, III) of endings in the geniculate neuropil. The large type I endings correspond to the retinal afferents which generally make asymmetric synapti contact with type II profiles and/or with clusters of microspines on the TSR dendrites. Type II, thought to be the spheroidal dendritic appendages of the PA neurons, form symmetrical synaptic contacts with profiles of its own kind or more commonly with dendrites of the TSR neuron. The type III ending, probably cortical in origin, establishes asymmetrical synaptic contacts with small dendritic profiles. Only profiles of types I and II endings, together with those of other dendritic profiles, form part of the nest-like junctions known as the synaptic glomeruli. The significance of the unusual polarization of the geniculate interneurons is discussed.     

Fine structure of the spinothalamic projections to the central lateral nucleus of the rat thalamus

The fine structure of labelled spinothalamic terminals in the central lateral nucleus has been studied in the rat following injection of wheat germ agglutinin-horseradish peroxidase into the spinal cord. Myelinated axons gave rise to the labelled terminals, which were large profiles which contained round vesicles, numerous mitochondria, and formed asymmetrical contacts with large dendrites or dendritic protrusions. These profiles are similar to those described in other somatosensory thalamic nuclei, and in many other nuclei of the thalamus.     

Early postnatal development of the monkey neostriatum: A Golgi and ultrastructural study

Paired specimens of the neostriatum were taken from monkeys at zero (newborn), one, two, four, eight, and 16 weeks of age, and prepared for Golgi impregnations and electron microscopy. Light microscopy shows that in the first postnatal week, the structure contains the five neuronal types and four categories of afferent axons described in the adult, as well as some cells too undifferentiated to classify. Most neurons exhibit immature dendritic features, including local enlargements, terminal growth cones with filopodia, and filiform processes. In spiny type I cells, various levels of maturity may coexist in regions of a single dendrite, in different dendrites of the same neuron, and among individual cells. Spine density increases progressively with age, but the relative distribution of spine types remains about the same. Spiny type II neurons show some decline in spine density, and generally mature sooner than spiny type I cells. The long axons of spiny neurons have varicosities which disappear at about eight weeks. In younger animals (newborn and one week), the dendrites of aspiny neurons (types I, II, and III) may have a “spiny” appearance, exhibiting many spine-like and filiform processes. Concurrently, the short axons vary in degree of arborization from very immature to well developed. Electron microscopy corroborates the developmental features recognized in the Golgi material: dendritic and axonal growth cones, filopodia and varicosities, as well as various stages of maturation in somata and dendrites. Degenerating elements, mostly of an axonal nature, are seen up to eight weeks. The synapses which reach maturity at birth are of the asymmetric axospinous type, in which the axonal profile contains small round vesicles, and of the symmetric axodendritic class, with the presynaptic elements having pleomorphic vesicles. Some synapses are slower to mature and appear at one to eight postnatal weeks. These include those made by profiles with pleomorphic vesicles, forming either symmetric contacts with somata and axon initial segments, or asymmetric contacts with spines. The same applies to the asymmetric axodendritic synapses made by elements containing small round vesicles. Finally, profiles containing large round or flat vesicles are the latest to participate in mature synapses formation. Findings indicate that a considerable degree of qualitative and quantitative change takes place in the monkey neostriatal neuropil during early postnatal development, especially in the first eight-week period.     

Ultrastructural features of NPY-containing neurons in the rat striatum

In the present study, we examined the ultrastructure of striatal neurons containing neuropeptide Y (NPY) which were labeled by an immunohistochemical method using peroxidase-conjugated F(ab) fragments in the rat. Each of the 26 neurons identified had a deeply indented oval nucleus. The cytoplasm, which was mainly concentrated at the emergence of the dendrites, contained an abundant Golgi apparatus and a well-developed granular endoplasmic reticulum. Dendrites were poorly branched and rarely exhibited varicosities or dendritic spines. NPY-immunoreactive (Ir) axons were small in diameter and unmyelinated. These features corresponded to a subpopulation of striatal neurons classified as aspiny type IV in previous Golgi studies. Axon terminals forming symmetrical synapses were numerous on the NPY-Ir perikarya and proximal dendrites. On distal NPY-Ir dendrites, synaptic contacts were mainly of the asymmetrical type, suggesting that NPY neurons are contacted by at least 2 categories of afferent fibers. Several NPY-Ir axonal processes and boutons were found to form symmetrical synapses with dendrites, dendritic spines and perikarya belonging to spiny type neurons. These data were consistent with the view that NPY may act as a neurotransmitter of striatal interneurons. Moreover, the frequent observation of NPY axonal processes in the close vicinity of striatal vessels suggested that NPY might also play a role in the control of cerebral vasomotricity. Thirty hours after intranigral injection of 6-hydroxydopamine to induce a degeneration of nigrostriatal dopamine terminals, some characteristic degenerative boutons were observed in close apposition to NPY-Ir cell bodies, suggesting that NPY neurons are under a direct nigrostriatal dopaminergic influence.