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      Deiters’ Nucleus. Its Role in Cerebellar Ideogenesis : The Ferdinando Rossi Memorial Lecture

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          Abstract

          Otto Deiters (1834–1863) was a promising neuroscientist who, like Ferdinando Rossi, died too young. His notes and drawings were posthumously published by Max Schultze in the book “Untersuchungen über Gehirn und Rückenmark.” The book is well-known for his dissections of nerve cells, showing the presence of multiple dendrites and a single axon. Deiters also made beautiful drawings of microscopical sections through the spinal cord and the brain stem, the latter showing the lateral vestibular nucleus which received his name. This nucleus, however, should be considered as a cerebellar nucleus because it receives Purkinje cell axons from the vermal B zone in its dorsal portion. Afferents from the labyrinth occur in its ventral part. The nucleus gives rise to the lateral vestibulospinal tract. The cerebellar B module of which Deiters’ nucleus is the target nucleus was used in many innovative studies of the cerebellum on the zonal organization of the olivocerebellar projection, its somatotopical organization, its microzones, and its role in posture and movement that are the subject of this review.

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          Most cited references66

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          Glycinergic projection neurons of the cerebellum.

          The cerebellum funnels its entire output through a small number of presumed glutamatergic premotor projection neurons in the deep cerebellar nuclei and GABAergic neurons that feed back to the inferior olive. Here we use transgenic mice selectively expressing green fluorescent protein in glycinergic neurons to demonstrate that many premotor output neurons in the medial cerebellar (fastigial) nuclei are in fact glycinergic, not glutamatergic as previously thought. These neurons exhibit similar firing properties as neighboring glutamatergic neurons and receive direct input from both Purkinje cells and excitatory fibers. Glycinergic fastigial neurons make functional projections to vestibular and reticular neurons in the ipsilateral brainstem, whereas their glutamatergic counterparts project contralaterally. Together, these data suggest that the cerebellum can influence motor outputs via two distinct and complementary pathways.
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            Climbing fiber microzones in cerebellar vermis and their projection to different groups of cells in the lateral vestibular nucleus.

            1. The projections from one of the paths (b-VF-SOCP) in the ventral spino-olivocerebellar system to the cortical b-zone located in the lateral part of the anterior lobe vermis and to the lateral vestibular nucleus (LVN) have been studied in cats with the spinal cord transected at C3 sparing only the contralateral ventral funiculus. The projection to the b-zone was studied by recording climbing fiber responses in single Purkinje cells on stimulation of limb nerves. The projections to the LVN, direct through climbing fiber collaterals and indirect through Purkinje cells, were studied by recordings EPSPs and IPSPs in LVN neurons. 2. The Purkinje cells in the b-zone were arbitrarily divided into five groups with different inputs and occupying different microzones each with a width of about 200 micron. On passing medially across the b-zone the microzones had the following input characteristics: 1. activation exclusively from hindlimb nerves, 2. short-latency activation from hindlimb and long-latency activation from forelimb nerves, 3. short-latency activation from hindlimb and forelimb nerves, 4. short-latency activation from forelimb and long-latency activation from hindlimb nerves, and 5. activation exclusively from forelimb nerves. 3. The five microzones projected to different groups of LVN neurons which occurred intermingled throughout the nucleus. The LVN neurons inhibited from a certain microzone were activated by the collaterals of the climbing fibers projecting to that microzone. 4. The organization of the spino-olivo-cerebello-vestibulo-spinal path is discussed. It is suggested that the microzone and collection of subcortical neurons represent the basic computational unit of the cerebellum.
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              Topography of Purkinje cell compartments and mossy fiber terminal fields in lobules II and III of the rat cerebellar cortex: spinocerebellar and cuneocerebellar projections.

              Z Ji, R. Hawkes (1994)
              The cerebellar cortex is histologically uniform by conventional staining techniques, but contains an elaborate topography. In particular, on the efferent side the cerebellar cortex can be subdivided into multiple parasagittal compartments based upon the selective expression by Purkinje cell subsets of various molecules, for example the polypeptide antigens zebrin I and II, and on the afferent side many mossy fibers terminate as parasagittal bands of terminals. The relationships between mossy fiber terminal fields and Purkinje cell compartments are important for a full understanding of cerebellar structure and function. In this study the locations of spino- and cuneocerebellar mossy fiber terminal fields in lobules II and III of the rat cerebellum are compared to the compartmentation of the Purkinje cells as revealed by using zebrin II immunocytochemistry. Wheat germ agglutinin-horseradish peroxidase was injected at three different levels in the spinal cord and in the external cuneate nucleus, and the terminal field distributions in lobules II and III of the cerebellar cortex were compared with the Purkinje cell compartmentation. In the anterior lobe, zebrin II immunocytochemistry reveals three prominent, narrow immunoreactive bands of Purkinje cells, P1+ at the midline and P2+ laterally at each side. These are separated and flanked by wide zebrin- compartments (P1- and P2-). There are also less strongly stained P3+ and P4+ bands more laterally. The spinocerebellar terminals in the granular layer are distributed as parasagittally oriented bands. Projections from the lumbar region of the spinal cord terminate in five bands, one at the midline (L1), a second with its medial border midway across P1- and its lateral border at the P2+/P2- interface (L2), and a third extending laterally from midway across P2-. The lateral edge of L3 may align with the P3+/P3- border. The terminal fields labeled by a tracer injection into the thoracic region give a very similar distribution (T1, T2 and T3). The only systematic difference is in T2, which statistical analysis suggests may be broader than L2. In contrast, anterograde tracer injections into the cervical region label synaptic glomeruli scattered throughout the lobule with much weaker or no evidence of banding. The terminal fields of the cuneocerebellar projection have a complementary distribution to those of thoracic and lumbar spinocerebellar terminals. There are two lateral bands, Cu2 and Cu3. Cu2 lies within the Purkinje cell P1-compartment, abutting L1/T1 medially and L2/T2 laterally. Cu3 lies between L2 and L3 within the P2- Purkinje cell compartment. The medial edge of Cu3 is tightly aligned with the P2+/P2- border.(ABSTRACT TRUNCATED AT 400 WORDS)
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                Author and article information

                Contributors
                janvoogd@bart.nl
                Journal
                Cerebellum
                Cerebellum
                Cerebellum (London, England)
                Springer US (New York )
                1473-4222
                1473-4230
                9 June 2015
                9 June 2015
                2016
                : 15
                : 54-66
                Affiliations
                Department of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands
                Article
                681
                10.1007/s12311-015-0681-9
                4726724
                26054378
                0bd33b59-3ff7-443f-a61f-39b26aa643f2
                © The Author(s) 2015

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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                © Springer Science+Business Media New York 2016

                Neurology
                deiters’ nucleus,lateral vestibulospinal tract,somatotopical organization,microzones,decerebrate rigidity

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