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Metabotrop glutamate receptor type 1a expressing unipolar brush cells in the cerebellar cortex of different species: A comparative quantitative study

Morphology, distribution and number of unipolar brush cells (UBCs) was studied in the cerebellar vermal lobules I–X of the chicken, rat, guinea pig, cat, and monkey using monoclonal mGluR1a antibody as a marker to visualise these recently described nerve cells (Mugnaini and Floris [1994] J. Comp. Ne...

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Published in:Journal of neuroscience research 1999-03, Vol.55 (6), p.733-748
Main Authors: Takács, József, Markova, Ljudmila, Borostyánköi, Zsolt, Görcs, Tamás J., Hámori, József
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description Morphology, distribution and number of unipolar brush cells (UBCs) was studied in the cerebellar vermal lobules I–X of the chicken, rat, guinea pig, cat, and monkey using monoclonal mGluR1a antibody as a marker to visualise these recently described nerve cells (Mugnaini and Floris [1994] J. Comp. Neurol. 339:174–180; Mugnaini et al. [1994] Synapse 16:284–311). The morphological appearance of mGluR1a immunopositive UBCs is similar in all species investigated: they are small cells, having a single, relatively short and thick dendrite, terminating in brush‐like dendrioles. Although this, probably excitatory, cell type can be found all over the cerebellar cortex, highest density of UBCs can be seen in the vermal cortex. The present study, therefore, was focused on the quantitative morphology and distribution of UBCs in the 10 lobules of the vermis. Calculating the number of UBCs/1 Purkinje cell (PC), we have found differences in this value (average in vermal lobules I–X) from 1.04 in rat, 1.10 in chicken, 1.16 in guinea pig, 2.27 in monkey, and up to 2.44 in cat. The highest density of UBCs was observed in lobules I, IX, and X, whereas the lowest number of UBCs/1 PC was found in lobules IV–VI (in the mammals) and in lobules VII–VIII (in the chicken). In mammals, particularly the monkey and cat, an increased presence of UBCs was observed in vermal sub‐lobules VIc–VIIb,c, a region defined as the oculomotor vermis because of its role in the control of saccadic eye movement. There is also a basic difference between chicken and mammals in the distribution of UBCs within the lobules: in mammals, the lowest density of these nerve cells was found in the peripheral portion of the lobules, near to the pia, while in the chicken, in contrast, the density of UBCs was the highest subpially with fewer UBCs located in the deepest curvature of the lobules. Finally, the functional significance of the differences in the density and in the distribution pattern of UBCs in the cerebellar vermis between the phylogenetically different species investigated is briefly discussed. J. Neurosci. Res. 55:733–748, 1999.  © 1999 Wiley‐Liss, Inc.
doi_str_mv 10.1002/(SICI)1097-4547(19990315)55:6<733::AID-JNR8>3.0.CO;2-8
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Comp. Neurol. 339:174–180; Mugnaini et al. [1994] Synapse 16:284–311). The morphological appearance of mGluR1a immunopositive UBCs is similar in all species investigated: they are small cells, having a single, relatively short and thick dendrite, terminating in brush‐like dendrioles. Although this, probably excitatory, cell type can be found all over the cerebellar cortex, highest density of UBCs can be seen in the vermal cortex. The present study, therefore, was focused on the quantitative morphology and distribution of UBCs in the 10 lobules of the vermis. Calculating the number of UBCs/1 Purkinje cell (PC), we have found differences in this value (average in vermal lobules I–X) from 1.04 in rat, 1.10 in chicken, 1.16 in guinea pig, 2.27 in monkey, and up to 2.44 in cat. The highest density of UBCs was observed in lobules I, IX, and X, whereas the lowest number of UBCs/1 PC was found in lobules IV–VI (in the mammals) and in lobules VII–VIII (in the chicken). In mammals, particularly the monkey and cat, an increased presence of UBCs was observed in vermal sub‐lobules VIc–VIIb,c, a region defined as the oculomotor vermis because of its role in the control of saccadic eye movement. There is also a basic difference between chicken and mammals in the distribution of UBCs within the lobules: in mammals, the lowest density of these nerve cells was found in the peripheral portion of the lobules, near to the pia, while in the chicken, in contrast, the density of UBCs was the highest subpially with fewer UBCs located in the deepest curvature of the lobules. Finally, the functional significance of the differences in the density and in the distribution pattern of UBCs in the cerebellar vermis between the phylogenetically different species investigated is briefly discussed. J. Neurosci. 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Neurosci. Res</addtitle><description>Morphology, distribution and number of unipolar brush cells (UBCs) was studied in the cerebellar vermal lobules I–X of the chicken, rat, guinea pig, cat, and monkey using monoclonal mGluR1a antibody as a marker to visualise these recently described nerve cells (Mugnaini and Floris [1994] J. Comp. Neurol. 339:174–180; Mugnaini et al. [1994] Synapse 16:284–311). The morphological appearance of mGluR1a immunopositive UBCs is similar in all species investigated: they are small cells, having a single, relatively short and thick dendrite, terminating in brush‐like dendrioles. Although this, probably excitatory, cell type can be found all over the cerebellar cortex, highest density of UBCs can be seen in the vermal cortex. The present study, therefore, was focused on the quantitative morphology and distribution of UBCs in the 10 lobules of the vermis. Calculating the number of UBCs/1 Purkinje cell (PC), we have found differences in this value (average in vermal lobules I–X) from 1.04 in rat, 1.10 in chicken, 1.16 in guinea pig, 2.27 in monkey, and up to 2.44 in cat. The highest density of UBCs was observed in lobules I, IX, and X, whereas the lowest number of UBCs/1 PC was found in lobules IV–VI (in the mammals) and in lobules VII–VIII (in the chicken). In mammals, particularly the monkey and cat, an increased presence of UBCs was observed in vermal sub‐lobules VIc–VIIb,c, a region defined as the oculomotor vermis because of its role in the control of saccadic eye movement. 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Neurosci. Res</addtitle><date>1999-03-15</date><risdate>1999</risdate><volume>55</volume><issue>6</issue><spage>733</spage><epage>748</epage><pages>733-748</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>Morphology, distribution and number of unipolar brush cells (UBCs) was studied in the cerebellar vermal lobules I–X of the chicken, rat, guinea pig, cat, and monkey using monoclonal mGluR1a antibody as a marker to visualise these recently described nerve cells (Mugnaini and Floris [1994] J. Comp. Neurol. 339:174–180; Mugnaini et al. [1994] Synapse 16:284–311). The morphological appearance of mGluR1a immunopositive UBCs is similar in all species investigated: they are small cells, having a single, relatively short and thick dendrite, terminating in brush‐like dendrioles. Although this, probably excitatory, cell type can be found all over the cerebellar cortex, highest density of UBCs can be seen in the vermal cortex. The present study, therefore, was focused on the quantitative morphology and distribution of UBCs in the 10 lobules of the vermis. Calculating the number of UBCs/1 Purkinje cell (PC), we have found differences in this value (average in vermal lobules I–X) from 1.04 in rat, 1.10 in chicken, 1.16 in guinea pig, 2.27 in monkey, and up to 2.44 in cat. The highest density of UBCs was observed in lobules I, IX, and X, whereas the lowest number of UBCs/1 PC was found in lobules IV–VI (in the mammals) and in lobules VII–VIII (in the chicken). In mammals, particularly the monkey and cat, an increased presence of UBCs was observed in vermal sub‐lobules VIc–VIIb,c, a region defined as the oculomotor vermis because of its role in the control of saccadic eye movement. There is also a basic difference between chicken and mammals in the distribution of UBCs within the lobules: in mammals, the lowest density of these nerve cells was found in the peripheral portion of the lobules, near to the pia, while in the chicken, in contrast, the density of UBCs was the highest subpially with fewer UBCs located in the deepest curvature of the lobules. Finally, the functional significance of the differences in the density and in the distribution pattern of UBCs in the cerebellar vermis between the phylogenetically different species investigated is briefly discussed. J. Neurosci. Res. 55:733–748, 1999.  © 1999 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>10220114</pmid><doi>10.1002/(SICI)1097-4547(19990315)55:6&lt;733::AID-JNR8&gt;3.0.CO;2-8</doi><tpages>16</tpages></addata></record>
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ispartof Journal of neuroscience research, 1999-03, Vol.55 (6), p.733-748
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1097-4547
language eng
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source Wiley-Blackwell Read & Publish Collection
subjects Animals
Cats
cerebellum
Cerebral Cortex - cytology
Cerebral Cortex - metabolism
Chickens
Dendrites - metabolism
Guinea Pigs
Immunohistochemistry
Macaca mulatta
mGluR1a
Neurons - classification
Neurons - cytology
Neurons - metabolism
Rats
Rats, Wistar
Receptors, Metabotropic Glutamate - analysis
Receptors, Metabotropic Glutamate - metabolism
Species Specificity
UBC
title Metabotrop glutamate receptor type 1a expressing unipolar brush cells in the cerebellar cortex of different species: A comparative quantitative study
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