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D K Morest

Publications and source records attributed to D K Morest.

At least 55 records · Page 3Linked to original sources
PubMed1991

Ganglion formation from the otic placode and the otic crest in the chick embryo: mitosis, migration, and the basal lamina.

We have studied the morphogenesis of the cochleo-vestibular (CVG) and distal cranial ganglia in the early chick embryo (White Leghorn embryos). Light microscopy and immunocytochemical staining for fibronectin and laminin were used to trace the cellular contributions to these ganglia from the otic placode and otocyst. Serial semi-thin plastic sections (3-5 microns) stained with toluidine blue at each Hamburger-Hamilton stage (St.) from 10 to 21 were used. We were able to trace individual groups of cells derived from these epithelial structures into the anlagen of the CVG and the distal parts of cranial n. ganglia VII, IX, and X. For immunostaining, antisera were used to visualize the basal lamina in 15-microns cryostat sections from St. 14 to 21 embryos. Described here for the first time is the otic crest, a ridge of epithelium surrounding the placode. Cells migrate from the otic crest (St. 11 to 14) during the period when the otocyst is forming. These cells become continuous spatially with those derived from the epibranchial placodes and the presumptive ganglia of cranial nerves VII, IX, and X. Furthermore, rostral otic crest cells merge with neural crest cells, which appose the myelencephalon, and they join with the newly formed neuroblasts of the CVG, which migrate from the ventral epithelium of the otocyst at St. 14 to 21. This region of the epithelium forms the bulk of the CVG; it also has many more mitotic figures than the rest of the otocyst. Cells in the rostralmost CVG (vestibular part) are the first to complete their migration and send axons into both the medulla and incipient crista ampullaris. Immuno-staining for fibronectin and laminin shows that these two basal-lamina-associated glycoproteins appear in a continuous layer beneath the otic epithelium just prior to CVG migration. Thus there is no evidence that the migration is launched by a prior decomposition of the basal lamina. The cells migrating from the epithelium bridge the basal lamina with their leading processes while the trailing processes are withdrawing from the epithelium. These trailing processes must withdraw after the neuroblast migrates, since most of the neuroblasts undergo mitosis in subsequent stages. The migrating cells appear to push out of the epithelium by displacing immunostained fragments of the basal lamina ahead of their leading processes. This suggests that the exodus of cells is accompanied by forces within the epithelium itself. Whether this is generated by the migratory neuroblasts themselves or by other sources remains to be determined.

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PubMed1991

Direct observation in vitro of how neuroblasts migrate: medulla and cochleovestibular ganglion of the chick embryo.

The hypothesis that neuroblasts migrate in the nervous system by a locomotory process was tested experimentally. An in vitro preparation permitted direct observation of postmitotic cells migrating from the rhombic lip of the medulla and the anlage of the cochleovestibular ganglion. Cell locomotion was not seen. Instead migration was produced by elongation of a leading process, followed by translocation of the nucleus (perikaryal translocation). On the basis of comparisons with previous observations in situ, we propose that this represents a common mode of migration in the developing nervous system. Cell clusters were explanted from the rhombic lip at the developmental stage when they migrate from the ventricular zone to the acoustico-vestibular anlage in the medulla. Cells from the cochleovestibular ganglion were explanted after migration from the otocyst, but before ganglionic differentiation. Each neuroblast's migration route was formed by an elongating leading process ending in a growth cone. The growth cone attached to other cells and processes or ended freely on an acellular substrate. Nonneuronal cells usually migrated as has been described for fibroblasts, yet with some of the features of perikaryal translocation, but some nonneuronal precursor cells may migrate the way neuroblasts do. Neuroblasts did not migrate preferentially on the processes of nonneuronal cells, although the reverse could be observed. In fact a variety of interactions between migratory cells, neuronal and nonneuronal, were observed. The advantage of the experimental system described here is that one can observe cells migrating spontaneously at the times in development when they normally do so, while preserving the cellular populations present in situ.

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PubMed1991

Glycine immunoreactive projections from the dorsal to the anteroventral cochlear nucleus.

The aim of the present study was to investigate whether projections from the dorsal cochlear nucleus (DCN) to the anteroventral cochlear nucleus (AVCN) use either of two inhibitory transmitters, glycine or GABA. Retrograde HRP labeling of DCN-to-AVCN projection neurons was combined with postembedding immunocytochemistry in the DCN of guinea pigs. Following injections of HRP in the anterior or posterior divisions of AVCN, large numbers of neurons were labeled in the DCN. All of these were located in the deep layer, except for a few granule cells. Nearly all (96%) of the projection neurons were immunoreactive for glycine and most had dendritic and somatic morphologies corresponding to those of elongate neurons (so-called 'corn' cells); only a few resembled small stellate neurons. Few (3%) retrogradely labeled neurons were immunoreactive for GABA. The results suggest that projections from the deep DCN to the AVCN are formed primarily by glycinergic elongate neurons. These projections could have a substantial inhibitory influence on the output of neurons in the AVCN.

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PubMed1990

Cytoarchitectonic atlas of the cochlear nucleus of the chinchilla, Chinchilla laniger.

A detailed cytoarchitectonic atlas of the chinchilla cochlear nucleus complex was prepared in the transverse plane with the Nissl method. Subdivisions of the cochlear nucleus were defined on the basis of cell size, cell packing density, and, in some cases, on cytological features of cell types. In general, the chinchilla cochlear nucleus has an organizational plan similar to that described for other mammalian species. As in other rodents, the chinchilla has a large and well-developed dorsal cochlear nucleus consisting of three distinct layers. The ventral cochlear nucleus consists of two distinct nuclear masses, a posterior nuclear group and an anterior nuclear group, each composed of several subdivisions, which are qualitatively similar to those described for other mammals. Thus it is now possible to compare detailed observations, such as tonotopic maps, in the chinchilla with findings from the analogous cell populations in other mammals, such as the cat, with considerable precision. In the chinchilla, three cell groups, previously undescribed in mammals, have been defined and their counterparts in the cat identified.

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PubMed1990

Migration of neuroblasts by perikaryal translocation: role of cellular elongation and axonal outgrowth in the acoustic nuclei of the chick embryo medulla.

The neuroblasts forming nucleus magnocellularis, the avian homologue of the mammalian ventral cochlear nucleus, migrate by growth and elongation of their leading processes and by perikaryal translocation through these processes from the matrix zone of the rhombic lip to the acoustico-vestibular anlage. Golgi methods were used on staged chick embryos to reconstruct the morphogenetic phases of migration and early differentiation in situ. Fluorescence labeling of the living cells in vitro elucidated the role of axonal growth in the migratory process. In situ, branching cochlear nerve fibers, tipped with growth cones, enter the acoustico-vestibular anlage at E4.5-5.5 before migration of the magnocellularis neuroblasts at E.5.5-6.5. The premigratory neuroblasts in the matrix zone of the rhombic lip resemble primitive epithelial cells, which extend branched, curving processes into a characteristic formation, the rhombic whorl. The leading process of the migrating magnocellularis neuroblasts gives rise to a bifurcating axon at the interface between the matrix and mantle zones. The lateral branch becomes the recurrent ipsilateral collateral; the medial branch crosses the midline, heading toward the contralateral target site in the region of the presumptive nucleus laminaris. The cell bodies of the migratory neuroblasts appear in intermediate locations along the migration route as they translocate radially through their leading processes past the axonal bifurcation and then tangentially and obliquely into the mantle zone. Neuroblasts destined for nucleus laminaris migrate coincidentally with magnocellularis neuroblasts. Nucleus angularis neuroblasts migrate later in development, after E6.5. In vitro, injections of a nontoxic fluorescent dye (diI) were made into explants of the medulla in the region of the contralateral target area at the time of neuroblast migration. DiI retrogradely labeled the cell bodies of premigratory magnocellularis neuroblasts in the matrix zone and of migratory neuroblasts in the mantle zone through their medial, crossing axonal branches. The morphology of the living neuroblasts in the explants resembled that in the Golgi impregnations at the corresponding stages of migration. Anterograde axonal transport also occurred. These results demonstrate migration by perikaryal translocation and early axon extension of a specific group of neuroblasts in the central nervous system. The morphology of the migrating neuroblasts is such that a simple radial arrangement of cellular guides, glial or otherwise, would not account for their configurations. The available evidence supports the proposition that cellular elongation and perikaryal translocation constitute the general mode of neuronal migration in the central nervous system. The early extension of axons into their target sites may play a critical role in migration and early development of specific types of neurons.

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PubMed1989

Glycine-immunoreactive projection of the cat lateral superior olive: possible role in midbrain ear dominance.

Neurons in the lateral superior olive are optimally excited by stimulation of the ipsilateral ear, as are those in the inferior colliculus by stimulation of the contralateral ear. This reversal of ear dominance may result, in part, from distinct crossed excitatory and uncrossed inhibitory pathways ascending from the lateral superior olive. To explore this possibility, immunoreactivity for two putative inhibitory neurotransmitters, glycine and GABA, was examined in projection neurons that retrogradely transported horseradish peroxidase from the cat inferior colliculus. The results suggest that the projection from the lateral superior olive can be segregated, immunocytochemically, into three components: 1) a crossed, glycine-negative (-) projection; 2) an uncrossed, glycine-positive (+) projection; and 3) an uncrossed, glycine(-) projection. Additional evidence suggests that the terminal fields of the two uncrossed projections may distribute differently within the inferior colliculus. Glycine(+) or glycine(-) projection neurons, crossed or uncrossed, do not differ in the size, shape, or location of their somata. However, most glycine(-) neurons are heavily encrusted with glycine(+) endings; glycine(+) neurons have 40-60% fewer of these endings. Glycine(-) neurons located in the lateral limb have fewer glycine (+) perisomatic endings than those in the medial limb. Few projection neurons are GABA(+), and GABA(+) perisomatic endings are rare in the lateral superior olive. Thus, there is a heavy uncrossed projection from the cat lateral superior olive to the inferior colliculus that may be glycinergic and inhibitory. Furthermore, there is a bilateral projection that is not glycinergic or GABAergic, which may be excitatory. The potential contribution of these pathways to contralateral ear dominance in the inferior colliculus is discussed.

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PubMed1989

Trophic support of the developing cochleovestibular ganglion by its peripheral target in vitro does not depend on neuronal cell division.

A trophic effect on the development of the cochleovestibular ganglion in the presence of its synaptic target tissue, the embryonic otocyst, has been shown in organ cultures. The basis for this trophic effect could be increased neuronal proliferation or enhanced postmitotic survival and differentiation. In order to determine if the trophic effect influenced neuronal proliferation, organ cultures of combined otocyst and cochleovestibular ganglion (embryonic stages 23-24) were grown 14 days in vitro in the continuous presence of [3H]thymidine. Serial sections of the explants made at each stage were assayed for autoradiographic labeling of cell nuclei and for numbers of cochleovestibular ganglion neurons. Explants were well developed morphologically and contained numbers of ganglionic neurons within the same range as previously reported. Many other well differentiated cell types were also present, including hair cells, supporting cells, other epithelial cells, cartilage, connective tissue, and perineuronal satellite cells. All of these non-neuronal cell types had undergone DNA synthesis in vitro, as evidenced by their heavily labeled nuclei. The cochleovestibular ganglion neurons were the only cell type with unlabeled nuclei, indicating that they had not divided or synthesized DNA during the two-week incubation. Thus all of the identifiable cochleovestibular ganglion neurons must have become postmitotic in the explants. Since ganglion cell division is still occurring in situ when the neurons are explanted, neuroblasts either failed to divide or failed to produce neuronal progeny in the culture conditions used. Therefore, the dependence of the cochleovestibular ganglion neurons on their normal target tissues most likely reflects a trophic effect on their postmitotic survival and differentiation.

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PubMed1989

A degenerative disorder of the central auditory system of the gerbil.

A previously unidentified disorder which affects primarily the cochlear nucleus was observed in two species of gerbils, Meriones unguiculatus and M. libycus. Unusual lesions were observed in the cochlear nucleus bilaterally in all animals examined. In light and electron microscopic specimens these lesions were characterized by the presence of microcysts and vacuolar neuronal degeneration. The microcysts resembled large holes, containing trabeculae, organelles and cellular remnants. Also observed were light and dark degeneration of neuronal perikarya and degenerated axons, dendrites, and synapses, accompanied by phagocytosis. Astrocytosis was not conspicuous. In the one cochlea examined, no microcysts were observed. In young animals the microcysts were prevalent in the cochlear nerve root region and the posteroventral cochlear nucleus. In older animals the microcysts increased in number and area. In the oldest animals, the microcysts had spread to other central auditory structures, including the superior olivary complex, the nuclei of the lateral lemniscus, and the inferior colliculus. Other regions of the brain were largely free of microcysts. The etiology and behavioral manifestations of this disorder are unknown, although it is clearly neurodegenerative and perhaps genetically determined.

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PubMed1989

The form and distribution of GABAergic synapses on the principal cell types of the ventral cochlear nucleus of the cat.

The distribution of GABAergic endings was examined histochemically in the ventral cochlear nucleus (VCN) of the cat using an antibody to glutamate decarboxylase (GAD), the synthetic enzyme for GABA. Immunoreactive (GAD+) endings appeared in all subdivisions of the cat VCN. Each of the principal cell types had a characteristic labeling pattern, based on the size, concentration, and distribution of GAD+ endings on its soma. Spherical bushy cell somata were typically contacted by many small (less than 1.5 microns in diameter) and medium-sized (1.5-2 microns in diameter) endings, many of which aggregated into tight clusters. Globular bushy cells had a similar pattern, but the clusters of GAD+ endings were less tightly packed. Reactive endings on stellate cells were more evenly distributed. GAD+ endings on octopus cells were larger (up to 2.5 microns in diameter) than those on the bushy cells and tended to aggregate into small clusters or rows on the somata and dendrites. Reactive endings contained small pleomorphic vesicles and formed symmetrical synaptic contacts on each of the cell types examined. The patterns formed by GAD+ endings on each type of neuron resemble those of certain types of non-cochlear axons previously described with the Golgi methods as projecting from the dorsal cochlear nucleus and the trapezoid body.

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PubMed1988

A cytoarchitectonic atlas of the medial geniculate body of the opossum, Didelphys virginiana, with a comment on the posterior intralaminar nuclei of the thalamus.

The organization of the medial geniculate body and adjacent posterior thalamus of the Virginia opossum was studied in Nissl-, Golgi-, reduced silver, and myelin-stained preparations. Our chief goals were to define the cytoarchitectonic subdivisions and boundaries in Nissl preparations and to reconcile these with those observed with the Golgi method and in experimental material, to present these results in an atlas of Nissl-stained sections, and to compare the chief nuclear groups in the opossum and the cat medial geniculate body. In the opossum, the ventral division consists chiefly of the ventral nucleus. The ventral nucleus is divided into two main parts: the pars lateralis and the pars ovoidea, the former being relatively smaller in the opossum. The ventral nucleus of both species contains large principal neurons with bushy, tufted dendrites and smaller Golgi type II cells. However, the opossum has far fewer Golgi type II cells, and the texture of the neuropil is correspondingly different, although the primary ascending input from the midbrain arises from the central nucleus of the inferior colliculus in both species. The dorsal division consists of the dorsal nuclei, including the suprageniculate nucleus and the caudal part of the lateral posterior nucleus, the marginal zone, and the posterior limitans nucleus. These nuclei are identified in both species, although they are much smaller in the opossum. The neurons consist of medium-size and small somata with a predominantly radiate mode of dendritic branching and a lower cell concentration than in the ventral division. In both species the afferent brain stem input comes from the inferior colliculus, the lateral tegmental area, the intercollicular tegmentum, and the superior colliculus. The medial division contains several types of cells, which are heterogeneous in form and size, most having radiating dendrites and a low cellular concentration. This division is especially smaller in the opossum, although comparable inputs arise from various auditory and non-auditory sources in the midbrain and spinal cord in both species. A large intralaminar complex of nuclei occurs in the opossum, which have a more extensive distribution than previously appreciated. They not only occupy the intramedullary laminae but form a shell around the medial geniculate nuclei and adjoining main sensory nuclei. The intralaminar complex includes the posterior limitans, posterior intralaminar, posterior, parafascicular, posterior parafascicular, central intralaminar, limitans, and central medial nuclei, and the marginal zone of the medial geniculate body.(ABSTRACT TRUNCATED AT 400 WORDS)

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PubMed1985

Trophic interactions between the cochleovestibular ganglion of the chick embryo and its synaptic targets in culture.

The effect of the availability of synaptic targets on neuronal survival was tested by explanting the cochleovestibular ganglion from embryonic day 3-1/2 chick embryos and maintaining it in the presence or absence of appropriate synaptic target tissues for 14 days in culture. The targets were the inner ear, peripherally, and the myelencephalon, centrally. Light and electron microscopic observations showed that the ganglion cells in the explants with targets present had generally achieved a degree of differentiation comparable to that of their counterparts in embryonic day 14 embryos. The variety of cell types seen in the normal embryonic day 14 ganglia was also evident in vitro. In ganglia explanted without peripheral or central targets, few neurons survived. Ganglia explanted with either peripheral or central target intact showed considerably better survival than those explanted without any target. Ganglia explanted with only the peripheral target (the inner ear) survived equally as well as those with both central and peripheral targets. Ganglia cultured with the central target (myelencephalon) did not survive as well as those with peripheral targets. The effect of the peripheral target on the ganglion was less clear-cut when ganglia were first dissected from their targets and then recombined in culture. However, the results of such experiments in which nerve fascicles were traced in serial sections from ganglia to target areas, suggest that the actual innervation of target cells, as well as proximity of ganglia to target tissues, could influence neuronal survival. Establishment of innervation appeared to be selective, in that the closest available target area was not always the one contacted by the ganglionic fibers. The present findings are consistent with a role of neuron-target cell interactions in supporting neuronal survival in the cochleovestibular ganglion of the chick embryo. Both the central and the peripheral targets are implicated in trophic interactions with the sensory neurons.

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PubMed1985

The development of innervation patterns in the avian cochlea.

The sequence of developmental events leading to the innervation of the cochlea and the differentiation of its receptor cells has been studied in chick embryos with Golgi methods. We describe the morphogenesis of cochlear ganglion cell peripheral processes from their appearance in early embryos to the formation of their mature endings on hair cells in the basilar papilla (organ of Corti) of prehatching chicks. In the stage of peripheral fiber outgrowth, embryonic days 3-5, the fibers emerge from the ganglion cell bodies and grow, in a uniform fashion, toward the undifferentiated receptor epithelium of the otocyst. In the stage of the invasion of the otocyst by the peripheral fibers, embryonic days 6-7, some fibers enter the epithelium directly after reaching it, others enter after traveling some distance longitudinally beneath its basal lamina. The invading fibers appear to encounter resistance at the basal lamina, but, once within the epithelium, at embryonic days 8-9, they form a surfeit of branches in columnar zones oriented radially toward the surface. In early synaptogenesis (embryonic days 8-9) hair cells first become apparent. They differentiate from primitive epithelial cells. These cells withdraw their basal processes, which appear to accompany the growing fibers into the superficial epithelium. At embryonic days 11-13, the stage of mid-synaptogenesis, the fibers develop large, bulbous, preterminal and terminal swellings, which are located below the bases of the hair cells; the surplus branches atrophy or withdraw. Efferent axons are first seen in the epithelium at this time. In late synaptogenesis (embryonic days 14-17), the preterminal swellings disappear and the endings transform into mature foot-shapes at the bases of the hair cells. These morphological changes during the development of the peripheral endings are comparable to those of cochlear axons in nucleus magnocellularis (cochlear nucleus). During mid-synaptogenesis, when the ganglion cells develop swellings in the periphery, their central axons ramify extensively. Late in synaptogenesis, while the peripheral swellings disappear, there is a corresponding condensation of the central terminals to form the end-bulbs of Held. Thus, specific connections of the cochlear ganglion cells and their target cells in the ear and brain may result from two sequential developmental phases: (1) loosely organized and overabundant initial growth of branches from the fibers entering their target tissue; (2) reorganization of these fibers with the disappearance or resorption of the surplus branches during the transformation of their endings into mature synaptic arrangements.(ABSTRACT TRUNCATED AT 400 WORDS)

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PubMed1985

The growth of cochlear fibers and the formation of their synaptic endings in the avian inner ear: a study with the electron microscope.

The developmental sequence of nerve-epithelial cell contacts, leading up to the formation of the mature receptoneuronal synapse, has been studied in the basilar papilla of chick embryos with electron microscopy. The receptor epithelium before innervation, on embryonic days 3-4, consists of a homogeneous population of primitive cells; hair cells and supporting cells cannot be distinguished. During innervation of the epithelium (embryonic days 5-7), the invading peripheral fibers of cochlear ganglion cells penetrate the basal lamina and form nerve-epithelial attachments with the epithelial cell bases. Once within the epithelium some fibers turn and spread in the transverse dimension across the basilar papilla through channels formed between the basal epithelial processes. Subsequently, nerve-epithelial attachments are observed more superficially within the epithelium. Hair cells and supporting cells differentiate during early synaptogenesis (embryonic days 8-9). Receptoneural synapses, possibly derived from the nerve-epithelial attachments formed during the innervation stage, are first seen during this period. They are characterized by symmetrical or asymmetrical membrane densities, separated by a cleft containing a dense material. At many of these junctions synaptic bodies, as well as dense-cored and coated vesicles, gather in the hair cells. During mid-synaptogenesis (embryonic days 11-13) the hair cells proliferate synaptic bodies, many of which are not located at receptoneural junctions. The preterminal portions of the sensory endings form large swellings, containing flocculent material, endoplasmic reticulum and vesicles. Late in synaptogenesis (embryonic days 15-17) the swellings disappear, while synaptic endings are transformed to foot-shaped terminals. In the hair cells, synaptic bodies not associated with junctions disappear. Efferent synapses are first seen during this period. This sequence of ultrastructural changes, which the developing sensory nerve endings and their target cells undergo in parallel, can be correlated with observations of Golgi preparations from a companion study. These correlations suggest that the innervation of the cochlea involves the following developmental processes. Initially the peripheral fibers of the ganglion cells grow directly toward the otocyst in fascicles. Having reached the base of the primitive receptor epithelium, the axonal endings, including some with growth cones, encounter a barrier in the basal lamina. When they enter some of the fibers attach to the basal end-feet of the primitive epithelial cells.(ABSTRACT TRUNCATED AT 400 WORDS)

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PubMed1985

Uptake and release of gamma-aminobutyric acid in the guinea pig cochlear nucleus after axotomy of cochlear and centrifugal fibers.

This study attempts to determine if gamma-aminobutyric acid (GABA) may be a transmitter of cochlear nerve fibers projecting from the cochlea to the cochlear nucleus, and of centrifugal fibers projecting to the cochlear nucleus via the trapezoid body and the acoustic striae of the medulla. The uptake and the electrically evoked release of exogenous [14C]GABA were measured, in vitro, in the three major subdivisions of the guinea pig cochlear nucleus; the anteroventral, posteroventral, and dorsal cochlear nuclei. These activities were compared using unlesioned animals, animals with bilateral cochlear ablations, and animals whose trapezoid body and acoustic striae were interrupted on the right side of the medulla. Subdivisions from unlesioned animals took up [14C]GABA, achieving concentrations in the tissues that were 11-19 times that in the medium. Electrical stimulation evoked a Ca2+-dependent release of [14C]GABA from each subdivision. Bilateral cochlear ablation, which presumably destroyed the cochlear nerve fibers, had no effect on [14C]GABA uptake and release. Section of the trapezoid body and the acoustic striae on the right side of the medulla typically severed all known connections of the right posteroventral and dorsal cochlear nuclei with the rest of the brain, but left intact many connections involved with the right anteroventral cochlear nucleus. This lesion partially depressed [14C]GABA uptake and release in the right posteroventral and dorsal cochlear nuclei, but not in the right anteroventral cochlear nucleus. These findings suggest that one or more of the centrifugal tracts projecting to the cochlear nucleus may be GABAergic, 88% or more of the cochlear nerve fibers probably are not GABAergic, and some neurons of the cochlear nucleus are probably GABAergic.

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PubMed1984

Axons of the dorsal division of the medial geniculate body of the cat: a study with the rapid Golgi method.

The arrangement of eight groups of axons afferent to the nuclei of the dorsal division of the medial geniculate body is described in rapid Golgi impregnations from young cats. Three kinds of axons travel predominantly in the brachium of the inferior colliculus and enter the medial geniculate body ventromedially: group I, thin axons resembling ivy tendrils ending along dendrites; group II, thicker axons with a sinuous course and few branches; group IV, coarse thick axons with grumous collaterals and massive peridendritic terminals near principal cells and interneurons. Three kinds of axons enter from the parabrachial region and pass laterally: group III, very thin axons with many collaterals forming dense terminal nests; group V, runcinate axons with sparse, thin collaterals; group VI, either medium-sized (group VIa) or thin (group VIb) smooth axons, perhaps corticofugal, and ending near principal neuron dendrites; group VII, thick axons, entering from the auditory radiation, with large, grapelike terminal arbors; and group VIII, thin and forming peridendritic festoons on principal cells after entering from the brachium of the superior colliculus. There appears to be some, though not complete, segregation of axons in the dorsal division nuclei. Thus axons of groups I, III, IV, and VI are found in each nucleus, although group VI axons are conspicuous in the superficial dorsal nucleus, and group IV endings are much more elaborate in the dorsal and deep dorsal nuclei than in the superficial dorsal nucleus. Each axon type has a specific pattern of terminal branches, which contributes to the texture of the neuropil in each nucleus. Golgi type II axons accentuate these textural differences. Thus each nucleus has a specific pattern of neuropil by virtue of the relative proportions of the different groups of axons ending there and the density and architecture of the axonal plexus. For example, both the dorsal nucleus and the deep dorsal nucleus receive the same groups of afferent axons, but the axonal plexus is more diffusely and evenly distributed in the dorsal nucleus, whereas the neuropil of the deep dorsal nucleus is highlighted by aggregates of grumous endings, more irregularities in the distribution of the axonal plexus, and many more fibers of passage. The extrinsic axons in the dorsal division come from the inferior and superior colliculi, the lateral tegmental system of the midbrain, and the cerebral cortex.(ABSTRACT TRUNCATED AT 400 WORDS)

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PubMed1984

The neuronal architecture of the inferior colliculus in the cat: defining the functional anatomy of the auditory midbrain.

This study defines anatomical subdivisions in Golgi-impregnated material from the inferior colliculus of the cat. The findings demonstrate that the inferior colliculus consists of a mosaic of morphologically distinct parts of neuropil. Each part is also characterized by a unique set of neuronal types. Each part of the inferior colliculus can be defined as tectal or tegmental on the basis of the fundamental pattern of dendritic branching. The main subdivisions of the auditory tectum are the central nucleus, the cortex, and the paracentral nuclei. The central nucleus is distinguished by its laminated neuropil composed of neurons with disc-shaped dendritic fields oriented in parallel arrays with the lemniscal axons. In contrast, the cortex is identified by its broad layers of loosely woven neuropil, which are orthogonal to those in the central nucleus and lack neurons with disc-shaped dendritic fields. The paracentral nuclei, so called because of their scattered arrangement around the central nucleus, are the commissural, dorsomedial, rostral pole, lateral, and ventrolateral nuclei. The main subdivisions of the auditory tegmentum are the pericollicular areas, the nucleus of the brachium of the inferior colliculus, and the sagulum. The pericollicular areas are intercollicular or subcollicular and separate the tectal division from the superior colliculus, central gray, and remaining portions of the tegmentum. The afferent projections to each tectal and tegmental subdivision, as observed in silver-degeneration experiments, distinguish the parcellations based on the Golgi findings. Subdivisions containing tectal cell types receive afferents predominantly from the auditory pathways, in contrast to subdivisions with tegmental cell types, which receive inputs from a wide variety of sources. This suggests a correlation between neuronal types and the nature of their inputs. This analysis of the subdivisions of the inferior colliculus differs from previous studies, especially those relying on Nissl stains. It is likely that subdivisions distinguished by the pattern of the neuropil differ functionally, since the structural components identified in the Golgi-impregnated material are essential parts of the synaptic organization of the auditory midbrain. Future physiological studies should benefit from approaches in which the cell types serve as the focus for the analysis.

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PubMed1984

The central nucleus of the inferior colliculus in the cat.

The central nucleus of the inferior colliculus in the cat is distinguished by its unique neuropil. In Golgi-impregnated material, it is composed primarily of neurons with disc-shaped dendritic fields arranged into parallel arrays, or laminae, complemented by the laminar afferent axons from the lateral lemniscus. Large, medium-large, medium, and small varieties of disc-shaped cells are distinguished on the basis of the size of the dendritic field and cell body size, dendritic diameter, and dendritic appendages. A second major class of neurons in the central nucleus are the stellate cells with dichotomously branched, spherical-shaped dendritic trees. Simple, complex, and small stellate cells can be distinguished by their size and by the complexity of the dendritic and axonal branching. Laminar afferent axons are recognized by the nests of collateral side branches and the grapelike clusters of terminal boutons--thick, thin, and intermediate-sized varieties are apparent. Other axon types include local collaterals of central nucleus neurons, some of which are distinguished by their frequent and complex collaterals. In the central nucleus, the configuration of the fibrodendritic laminae, the presence of subdivisions, and the banding of afferent axons suggest levels of organization which are superimposed on the synaptic arrangements of the individual cell and axon types. The laminar pattern, as studied in serial Golgi-impregnated sections, differs from previous reports. The central nucleus contains subdivisions which can be distinguished by their laminar pattern, different proportions of cell types, and the packing density of the cell bodies and axonal plexus. The patterns of degeneration observed in Nauta-stained material after lesions of caudal auditory pathways show that thick and fine afferent fibers form dense bands of degeneration separated by sparse, fine-fiber degeneration. The bands are thicker than individual laminae but smaller than the subdivisions. The intrinsic organization of the neurons and axons, combined with the laminar organization, subdivisions, and banding patterns, each may contribute different aspects to the processing of auditory information in the central nucleus.

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