Basket cell axons don't reach to the Purkinje cells in the deep part of the central mass of the reeler cerebellum

1991 ◽  
Vol 16 ◽  
pp. 108
Author(s):  
Chitoshi Takayama ◽  
Yoshiro Inoue
2021 ◽  
Author(s):  
Hideki Miwa ◽  
Ken Kobayashi ◽  
Shinobu Hirai ◽  
Mitsuhiko Yamada ◽  
Masahiko Watanabe ◽  
...  

2020 ◽  
Author(s):  
Hideki Miwa ◽  
Ken Kobayashi ◽  
Shinobu Hirai ◽  
Mitsuhiko Yamada ◽  
Masahiko Watanabe ◽  
...  

Abstract Gamma-aminobutyric acid (GABA) is a major inhibitory neurotransmitter in the central nervous system, synthesized by two isoforms of glutamate decarboxylase (GAD): GAD65 and GAD67. GABA may act as a trophic factor during brain development, but its contribution to the development and maturation of cerebellar neural circuits is not known. To understand the roles of GABA in cerebellar development and associated functions in motor coordination and balance, we examined GAD65 conventional knock out (KO) mice and mice in which GAD67 was eliminated in parvalbumin-expressing neurons ( PV-Cre ; GAD67 flox/flox mice). We found aberrant subcellular localization of the Shaker-type K channel Kv1.1 in basket cell collaterals of PV-Cre ; GAD67 flox/flox mice and abnormal projections from basket cells to Purkinje cells in both mouse strains. Furthermore, PV-Cre ; GAD67 flox/flox mice exhibited abnormal motor coordination in the rotarod test. These results indicate that GABA signaling in the cerebellum during development is critical for establishing appropriate connections between basket cells and Purkinje cells and is associated with motor coordination in mice.


2011 ◽  
Vol 71 ◽  
pp. e215
Author(s):  
Ryoichi Ichikawa ◽  
Miwako Yamasaki ◽  
Taisuke Miyazaki ◽  
Haruyuki Tatsumi ◽  
Masahiko Watanabe

The cerebellum of the homozygous reeler mouse shows a marked reduction in size and in the number of fissures, its dry mass and DNA content are respectively and j—J of those of normal animals. Its high content in the P400 protein, which is abundant in the Purkinje cell, indicates that the decrease in cell number associated with the fall in DNA affects primarily the granular cells. The anatomy of the reeler cerebellum is rather unique: a thin cortex with almost normal molecular, granular and Purkinje cell layers embracing a central mass of closely packed large neurons, mostly Purkinje cells. Purkinje cells may therefore be found in four different cellular environments: (1) at their normal position in the superficial cortical structure; (2) within the granular layer; (3) intermingled with white matter in the central mass; (4) overlapping with neurons of the deep cerebellar nuclei. The reeler cerebellum therefore offers a model to study to what extent local cellular interactions are required to achieve the planar organization of the Purkinje cell dendrites and the normal synaptic investment of these cells. Concerning the three-dimensional shape of Purkinje cells, only the rare ones located at their normal position and receiving a normal ratio of all their synaptic afferences succeed to develop a characteristic dendritic pattern. Purkinje cells within the granular layer show three distinct patterns of dendritic arrangements. The variation in shape of the Purkinje cell dendrites located in the central agranular mass mimics that described in other agranular cerebella: in particular they show randomly oriented dendrites devoid of spiny branchlets. Concerning the cerebellar circuitry, the specificity of most of the synaptic connections is preserved, despite important disorders in Purkinje cell distribution.Several important differences with the normal cerebellum have, however, been observed at the level of the Purkinje cell: (i) The density of climbing fibre varicosities increases in the central cerebellar mass, where Purkinje cells are deprived of parallel fibre afferences. In addition, electrophysiological studies reveal that, at this position, the response of the Purkinje cells to climbing fibre stimulation is graded by steps as a function of stimulus intensity instead of being all-or-none as found in the superficial cortex or in normal cerebellum. These deep Purkinje cells receive therefore several climbing fibres instead of only one as in normal adult cerebellum, (ii) Ectopic synapses (somato-dendritic and dendro-dendritic) between the soma and/or the dendrite of the granule cell as presynaptic element and mainly the Purkinje cell dendrites as postsynaptic element may form, (iii) Heterologous synapses between mossy fibres and Purkinje cell spines are found in the granular layer and within the central mass. The electrophysiological studies show that these synapses are functional.


Author(s):  
Joy Zhou ◽  
Amanda M. Brown ◽  
Elizabeth P. Lackey ◽  
Marife Arancillo ◽  
Tao Lin ◽  
...  

AbstractRamón y Cajal proclaimed the neuron doctrine based on circuit features he exemplified using cerebellar basket cell projections. Basket cells form dense inhibitory plexuses that wrap Purkinje cell somata and terminate as pinceaux at the initial segment of axons. Here, we demonstrate that HCN1, Kv1.1, PSD95 and GAD67 unexpectedly mark patterns of basket cell pinceaux that map onto Purkinje cell functional zones. Using cell-specific genetic tracing with an Ascl1CreERT2 mouse conditional allele, we reveal that basket cell zones comprise different sizes of pinceaux. We tested whether Purkinje cells instruct the assembly of inhibitory projections into zones, as they do for excitatory afferents. Genetically silencing Purkinje cell neurotransmission blocks the formation of sharp Purkinje cell zones and disrupts excitatory axon patterning. The distribution of pinceaux into size-specific zones is eliminated without Purkinje cell output. Our data uncover the cellular and molecular diversity of a foundational synapse that revolutionized neuroscience.


eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Joy Zhou ◽  
Amanda M Brown ◽  
Elizabeth P Lackey ◽  
Marife Arancillo ◽  
Tao Lin ◽  
...  

Ramón y Cajal proclaimed the neuron doctrine based on circuit features he exemplified using cerebellar basket cell projections. Basket cells form dense inhibitory plexuses that wrap Purkinje cell somata and terminate as pinceaux at the initial segment of axons. Here, we demonstrate that HCN1, Kv1.1, PSD95 and GAD67 unexpectedly mark patterns of basket cell pinceaux that map onto Purkinje cell functional zones. Using cell-specific genetic tracing with an Ascl1CreERT2 mouse conditional allele, we reveal that basket cell zones comprise different sizes of pinceaux. We tested whether Purkinje cells instruct the assembly of inhibitory projections into zones, as they do for excitatory afferents. Genetically silencing Purkinje cell neurotransmission blocks the formation of sharp Purkinje cell zones and disrupts excitatory axon patterning. The distribution of pinceaux into size-specific zones is eliminated without Purkinje cell GABAergic output. Our data uncover the cellular and molecular diversity of a foundational synapse that revolutionized neuroscience.


2011 ◽  
Vol 31 (47) ◽  
pp. 16916-16927 ◽  
Author(s):  
R. Ichikawa ◽  
M. Yamasaki ◽  
T. Miyazaki ◽  
K. Konno ◽  
K. Hashimoto ◽  
...  

Author(s):  
R.V.W. Dimlich ◽  
M.H. Biros

In severe cerebral ischemia, Purkinje cells of the cerebellum are one of the cell types most vulnerable to anoxic damage. In the partial (forebrain) global ischemic (PGI) model of the rat, Paljärvi noted at the light microscopic level that cerebellar damage is inconsistant and when present, milder than in the telencephalon, diencephalon and rostral brain stem. Cerebellar injury was observed in 3 of 4 PGI rats following 5 minutes of reperfusion but in none of the rats after 90 min of reperfusion. To evaluate a time between these two extremes (5 and 90 min), the present investigation used the PGI model to study the effects of ischemia on the ultrastructure of cerebellar Purkinje cells in rats that were sacrificed after 30 min of reperfusion. This time also was chosen because lactic acid that is thought to contribute to ischemic cell changes in PGI is at a maximum after 30 min of reperfusion.


Author(s):  
R.V.W. Dimlich ◽  
M.H. Biros

Although a previous study in this laboratory determined that Purkinje cells of the rat cerebellum did not appear to be damaged following 30 min of forebrain ischemia followed by 30 min of reperfusion, it was suggested that an increase in rough endoplasmic reticulum (RER) and/or polysomes had occurred in these cells. The primary objective of the present study was to morphometrically determine whether or not this increase had occurred. In addition, since there is substantial evidence that glial cells may be affected by ischemia earlier than other cell types, glial cells also were examined. To ascertain possible effects on other cerebellar components, granule cells and neuropil near Purkinje cells as well as neuropil in the molecular layer also were evaluated in this investigation.


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