摘要:

AbstractShort‐survival thymidine radiograms from rat embryos aged 13–19 days were analyzed to delineate the precerebellar neuroepithelium of the rhombencephalon. The original definition of the term “rhombencephalon” was modified to refer only to the unique dorsal portion (surface plate) of the medulla and pons where the neural groove fails to fuse and, instead, the medullary velum covers the rhomboid lumen of the fourth ventricle. Initially, the neuroepithelial tissue of the rhombencephalon consists of a pair of rostral and caudal bridgeheads: the former the primary neuroepithelium of the cerebellum and the latter the primary neuroepithelium of the octavo‐precerebellar system. The spatial relationship between the cerebellar and precerebellar neuroepithelia soon changes as a result of ongoing morphogenetic events, such that the cerebellar primordium assumes a dorsal position and the precerebellar primordium a ventral position, and the distance between the two decreases. Concurrently the tela choroidea invaginates into the fourth ventricle and a secondary precerebellar neuroepithelium develops. The rostral portion of the secondary precerebellar neuroepithelium grows forward along the choroid plexus and forms the medial recess of the anterior fourth ventricle, while its caudal portion grows in the opposite direction beneath the medullary velum and forms the rostral wall of the posterior fourth ventricle. Evidence will be presented in the succeeding papers that the primary precerebellar neuroepithelium first generates the neurons of the inferior olive that migrate by a circumferential intramural (parenchymal) route to their destination. Next, the neurons of the lateral reticular and external cuneate nuclei are generated. These migrate by a posterior extramural (superficial) route and settle contralaterally. Subsequently, the primary precerebellar neuroepithelium produces the neurons of the nucleus reticularis tegmenti pontis and these form the anterior extramural migratory stream and settle ipsilaterally. Finally, the secondary precerebellar neuroepithelium produces the latest generated neurons of the basal pontine gray that follow the anterior extramural stream and settle ipsi

ISSN:0092-7317    

DOI:10.1002/cne.902570402

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

摘要:

AbstractSequential thymidine radiograms from rats labeled on days E13 and E14, and killed at daily intervals thereafter, were analyzed to trace the migratory route and settling pattern of neurons of the inferior olive. Long‐survival thymidine radiograms from perinatal rats injected on day E14 were used to subdivide the inferior olivary complex on the basis of neurogentic criteria.The inferior olivary neurons originate on days E13 and E14 in the primary precerebellar neuroepithelium. The olivary neurons labeled on day E14 (the late generated components) translocate into the inferior olivary premigratory zone on day E15. On day E16 these cells join the olivary migratory stream, which follows an intramural circumferential path between the gray and white matters of the medulla. By day E17 the olivary migratory stream is reduced to a small band near the corpus of the inferior olive, which has been settled by this time by neurons generated on day E13. As a result, the unlabeled cells are situated on day E17 dorsomedially and the labeled cells ventrolaterally. The regional segregation of neurons forming subdivisions of the inferior olive begins on day E18, and by day E19 the major subdivisions are all recognizable.In thymidine radiograms from perinatal rats injected on day E14, four neurogenetic components can be distinguished in the inferior olive, those composed: (1) of unlabeled cells (generated on day E13), (2) of predominantly unlabeled cells, (3) of predominantly labeled cells (generated on day E14), and (4) of labeled cells. By combining these neurogenetic differences with the morphological features of the inferior olivary complex, we propose a modification of the currently accepted classification. The four major divisions of the inferior olive are the successively produced posterodorsal olive, anterolateral (principal) olive, posteroventral olive, and anteroventral olive. The location and configuration of these divisions are illustrated in relation to the traditional classification both in the coronal and the sagittal plan

ISSN:0092-7317    

DOI:10.1002/cne.902570403

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

摘要:

AbstractSequential thymidine radiograms from rats injected on day E15 and killed thereafter at daily intervals up to day E22 were analyzed to trace the migratory routes and settling patterns of neurons of the lateral reticular nucleus and the external cuneate nucleus. The neurons of the lateral reticular and external cuneate nuclei originate in the primary precerebellar neuroepithelium at the same site as the inferior olivary neurons but follow a different migratory route. The labeled young neurons that are produced on day E15 (the last one‐third of the total) join the posterior precerebellar extramural migratory stream. The cells move circumferentially over the wall of the medulla in a ventral direction and by day E17 reach the midline and cross it beneath the inferior olive. The crossing cells apparently continue to migrate circumferentially on the opposite side. One complement of these cells begins to form a ventrolateral extramural condensation on day E19. By day E20 some cells begin to penetrate the parenchyma and settle as neurons of the lateral reticular nucleus. The settling of the lateral reticular neurons continues on the following day, and by day E22 all the cells destined for the lateral reticular nucleus have penetrated the parenchyma. A dorsomedial‐to‐ventrolateral neurogenetic gradient is indicated for the settling lateral reticular neurons.Another complement of migrating cells continues dorsally and forms a condensation on day E19 that we interpret as the external cuneate component of the crossed stream. These cells begin to penetrate the parenchyma on day E20, and by days E21 and E22 two components of the external cuneate nucleus are identifiable–the dorsal and ventral external cuneate nuclei. The neurons of the lateral reticular and external cuneate nuclei differ from neurons of all the other precerebellar nuclei in that their cerebellar projection is predominantly ipsilateral. We speculate that the axons of all precerebellar neurons are genetically specified to cross the midline ventrally to provide a contralateral efferent projection, but this is modified in the case of the ipsilaterally projecting lateral reticular and external cuneate neurons by the cell bodies following their neurites to the opposi

ISSN:0092-7317    

DOI:10.1002/cne.902570404

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

摘要:

AbstractSequential thymidine radiograms from rats injected on days E16, E17, E18, and E19 and killed 2 hours after injection and at daily intervals up to day E22 were used to establish the site of origin, migratory route, and settling patterns of neurons of the nucleus reticularis tegmenti pontis and basal pontine gray. The nucleus reticularis tegmenti pontis neurons, which are produced predominantly on days E15 and E16, derive from the primary precerebellar neuroepithelium. These cells, unlike those of the lateral reticular and external cuneate nuclei, take an anteroventral subpial route, forming the anterior precerebellar extramural migratory stream. This migratory stream reaches the anterior pole of the pons by day E18. In rats injected on day E16 and killed on day E18 some of the cells that reach the pons are unlabeled, indicating that they represent the early component of neurons generated on day E15. The cells labeled on day E16 begin to settle in the pons on day E19, 3 days after their production. These cells, migrating in an orderly temporal sequence, form a posterodorsal‐to‐anteroventral gradient in the nucleus reticularis tegmenti pontis.Unlike the neurons of all the other precerebellar nuclei, the basal pontine gray neurons derive from the secondary precerebellar neuroepithelium. The secondary precerebellar neuroepithelium forms on day E16 as an outgrowth of the primary precerebellar neuroepithelium, and it remains mitotically active through day E19, spanning the entire period of basal pontine gray neurogenesis. The secondary precerebellar neuroepithelium is surrounded by a horizontal layer of postmitotic cells, representing the headwaters of the anterior precerebellar extramural migratory stream. In rats injected on day E18 and killed on day E19 the cells are labeled in the proximal half of the stream around the medulla but those closer to the pons are unlabeled, indicating an orderly sequence of migration. In rats injected on day E18 and killed on day E20 the labeled cells reach the pole of the pons. In the basal pontine gray the sequentially generated neurons settle in a precise order. The neurons generated on day E16 form a small core posteriorly and the neurons generated on days E17, E18, and E19 form regular concentric rings around the core in an inside‐out seq

ISSN:0092-7317    

DOI:10.1002/cne.902570405

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

摘要:

AbstractAfferent and efferent connections of the limb specific divisions of the cat magnocellular red nucleus (RNm) were traced using the bidirectional transport of wheatgerm agglutinin‐horseradish peroxidase complex (WGA‐HRP). Injection sites within forelimb or hindlimb RNm regions were identified by microelectrode recording and confirmed by the position of labeled rubrospinal terminals. Additional injections into structures that project to, or receive input from, RNm confirmed the somatotopic organization of these pathways.The forelimb region of RNm receives input from the posteriolateral part of the anterior interpositus nucleus (NIA) and the intermediate part of the posterior interpositus nucleus (NIP). The hindlimb region of RNm receives input from anteriomedial NIA and medial NIP. Terminals of NIA cells densely fill all of RNm, but terminals of NIP cells form a half shell on the medial, ventral, and posterior borders of RNm without encroaching on RNm's lateral edge or central core. Forelimb and hindlimb RNm are reciprocally connected with the caudal cuneate and gracile nuclei respectively. There is little or no input to RNm from the medial or lateral cerebellar nuclei.Forelimb RNm, which also contains a face representation, projects to the lateral reticular nucleus, cell group f of the inferior vestibular nucleus, the facial nucleus, the main sensory nucleus of the trigeminal nerve, the caudal cuneate nucleus, the parvicellular reticular formation, and cervical segments of the spinal cord. A few fibers from forelimb RNm project directly to motor neurons in the lower cervical cord. Hindlimb RNm projects to only the lateral reticular nucleus, gracile nucleus, and lower spinal segments. Forelimb and hindlimb RNm project to different regions of the lateral reticular nucleus with some over

ISSN:0092-7317    

DOI:10.1002/cne.902570406

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

摘要:

AbstractThe relationship of the varicosities of sympathetic postganglionic nerve terminals to the smooth muscle cells of arterioles in the submucosa of the guinea pig ileum has been investigated quantitatively by electron microscopy. Longitudinal sections were cut through arterioles about 50 m̈m in diameter after fixationin vitroorin situunder pressure. About 13% of the varicosities in individual ultrathin sections made contact with the outer surface of the smooth muscle cells. The neuromuscular junctions resembled those in skeletal muscle: the basal laminae of the axon bundle and of the smooth muscle were fused, and synaptic vesicles were accumulated close to the region of fusion. When individual varicosities were examined in serial sections, 92% and 83% in two preparations were found to form junctions of this kind. Most of the noncontacting varicosities were bare of Schwann cell toward the arteriolar surface and separated from it by>200 nm. Almost all axon profiles contained synaptic vesicles with electron dense cores after exposure to 5‐hydroxydopamine. In electrophysiological experiments, ionophoretic application of noradrenaline to the arteriolar surface along the nerve bundles (demonstrated subsequently by fluorescence histochemistry) produced responses resembling those evoked by nerve stimulation. These anatomical and physiological data, taken together with the evidence for quantal release in this preparation (see Hirst et al., '85), suggest that neuromuscular transmission involves the rare release of a quantum of noradrenaline at discrete points on the smooth muscle membra

ISSN:0092-7317    

DOI:10.1002/cne.902570407

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

摘要:

AbstractThe neuronal organization of the paraventricular nucleus (PVN) was examined in Golgi impregnations of adult monkey. Results showed that at least six types of neurons could be identified in the nucleus on the basis of morphological features of the somata, dendrites, and axons. Four types of neurons with sparse to densely spined cell bodies and dendrites exhibited long axons and included large neurons (types I and II), medium‐sized to large neurons (type III), and small to medium‐sized cells (type IV). Axons of type I, III, and IV neurons had different diameters and were followed out of the PVN. Axon collaterals that arborized within the PVN were seen on the axons of types III and IV cells. Two types of interneurons with small somata were also found. One (type V) exhibited varicose dendrites and a profusely arborizing local axon. The other cell (type VI) had recurved dendrites with long appendages and no impregnated axon. Afferent fibers were also identified. Type 1 was a fine‐caliber axon that coursed long distances in the PVN and exhibited numerous short branches. Additional observations suggested that type 1 afferents originated from the stria terminalis. The other afferent axon (type 2) was thicker and gave rise to terminal arborizations containing clusters of small swellings.The efferent fibers of the>PVN were also examined in impregnations of the paraventriculosupraopticohypophysial tract. Fibers formed an extensive plexus as they coursed ventrally and passed through the lateral hypothalamus. Axons coursing more laterally in the tract were much larger than those more medially located.Our findings show a diverse organization of neuronal types within the monkey PVN with evidence for intrinsic connections through axon collaterals of efferent neurons and the locally arborizing axons of interneurons. Correlations are proposed between morphological subtypes of neurons seen in this Golgi study and the known functional output pathways of th

ISSN:0092-7317    

DOI:10.1002/cne.902570408

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

摘要:

AbstractWe examined possible contributions of neurogenesis to sex differences in the vocalization pathway of the South African clawed frog,Xenopus laevis. Birthdates of neurons were obtained from autoradiograms of animals receiving tritiated thymidine from gastrulation through 1 month after metamorphosis. Thymidine availability studies showed that 80% of the [3H]‐thymidine injected into embryos and tadpoles was incorporated into the DNA of dividing cells within 3 hours. We observed 3 patterns of neurogenesis:late‐short, a short burst of proliferation occurred late in development in the anterior preoptic area, the ventromedial nucleus of the thalamus, and the pretrigeminal nucleus of the dorsal tegmental area of the medulla;protracted‐bimodal, a prolonged period of proliferation with an early and a late peak in the number of labeled cells occurred in the ventral striatum and in the ventrolateral and posterior nuclei of the thalamus;protracted‐unimodal, a prolonged period of proliferation with a single early peak occurred in the inferior reticular formation and in the medial and lateral nucleus IX‐X (containing laryngeal motor neurons). There were no differences between sexes in the number of tritiated thymidine labeled cells in any nucleus. The difference in nucleus IX‐X neuron number in adults does not appear to result from sex differences in the proliferation of these cells during development. Since neurons in the vocalization pathway do not exhibit androgen receptors until after neurogenesis is complete, we also conclude that androgen probably does not regulate the genesis of

ISSN:0092-7317    

DOI:10.1002/cne.902570409

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY

ISSN:0092-7317    

DOI:10.1002/cne.902570401

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1987

数据来源: WILEY