Survival of interneurons and parallel fiber synapses in a cerebellar cortex deprived of Purkinje cells: Studies in the double mutant mouse Grid2Lc/+;Bax

The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target‐related death of 90% of the granule cells and 60–75% of the olivary neurons. Inactivation of Bax, a pro‐apoptotic gene of the Bcl‐2 family, in heterozygous Lurcher mutant...

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Published inJournal of comparative neurology (1911) Vol. 497; no. 4; pp. 622 - 635
Main Authors Zanjani, S. Hadi, Selimi, Fekrije, Vogel, Michael W., Haeberlé, Anne-Marie, Boeuf, Julien, Mariani, Jean, Bailly, Yannick J.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.08.2006
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Abstract The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target‐related death of 90% of the granule cells and 60–75% of the olivary neurons. Inactivation of Bax, a pro‐apoptotic gene of the Bcl‐2 family, in heterozygous Lurcher mutants (Grid2Lc/+) rescues ∼60% of the granule cells, but does not rescue Purkinje or olivary neurons. Given the larger size of the cerebellar molecular layer in Grid2Lc/+;Bax−/− double mutants compared to Grid2Lc/+ mutants, we analyzed the survival of the stellate and basket interneurons as well as the synaptic connectivity of parallel fibers originating from the surviving granule cells in the absence of their Purkinje cell targets in the Grid2Lc/+;Bax−/− cerebellum. Quantification showed a significantly higher density of interneurons (∼60%) in the molecular layer of the Grid2Lc/+;Bax−/− mice compared to Grid2Lc/+, suggesting that interneurons are subject to a BAX‐dependent target‐related death in the Lurcher mutants. Furthermore, electron microscopy showed the normal ultrastructural aspect of a number of parallel fibers in the molecular layer of the Grid2Lc/+; Bax−/− double mutant mice and preserved their numerous synaptic contacts on interneurons, suggesting that interneurons could play a trophic role for axon terminals of surviving granule cells. Finally, parallel fibers varicosities in the double mutant established “pseudo‐synapses” on glia as well as displayed autophagic profiles, suggesting that the connections established by the parallel fibers in the absence of their Purkinje cell targets were subject to a high turnover involving autophagy. J. Comp. Neurol. 497:622–635, 2006. © 2006 Wiley‐Liss, Inc.
AbstractList The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target‐related death of 90% of the granule cells and 60–75% of the olivary neurons. Inactivation of Bax, a pro‐apoptotic gene of the Bcl‐2 family, in heterozygous Lurcher mutants (Grid2Lc/+) rescues ∼60% of the granule cells, but does not rescue Purkinje or olivary neurons. Given the larger size of the cerebellar molecular layer in Grid2Lc/+;Bax−/− double mutants compared to Grid2Lc/+ mutants, we analyzed the survival of the stellate and basket interneurons as well as the synaptic connectivity of parallel fibers originating from the surviving granule cells in the absence of their Purkinje cell targets in the Grid2Lc/+;Bax−/− cerebellum. Quantification showed a significantly higher density of interneurons (∼60%) in the molecular layer of the Grid2Lc/+;Bax−/− mice compared to Grid2Lc/+, suggesting that interneurons are subject to a BAX‐dependent target‐related death in the Lurcher mutants. Furthermore, electron microscopy showed the normal ultrastructural aspect of a number of parallel fibers in the molecular layer of the Grid2Lc/+; Bax−/− double mutant mice and preserved their numerous synaptic contacts on interneurons, suggesting that interneurons could play a trophic role for axon terminals of surviving granule cells. Finally, parallel fibers varicosities in the double mutant established “pseudo‐synapses” on glia as well as displayed autophagic profiles, suggesting that the connections established by the parallel fibers in the absence of their Purkinje cell targets were subject to a high turnover involving autophagy. J. Comp. Neurol. 497:622–635, 2006. © 2006 Wiley‐Liss, Inc.
The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target-related death of 90% of the granule cells and 60-75% of the olivary neurons. Inactivation of Bax, a pro-apoptotic gene of the Bcl-2 family, in heterozygous Lurcher mutants (Grid2Lc/+) rescues approximately 60% of the granule cells, but does not rescue Purkinje or olivary neurons. Given the larger size of the cerebellar molecular layer in Grid2Lc/+;Bax(-/-) double mutants compared to Grid2Lc/+ mutants, we analyzed the survival of the stellate and basket interneurons as well as the synaptic connectivity of parallel fibers originating from the surviving granule cells in the absence of their Purkinje cell targets in the Grid2Lc/+;Bax(-/-) cerebellum. Quantification showed a significantly higher density of interneurons ( approximately 60%) in the molecular layer of the Grid2Lc/+;Bax(-/-) mice compared to Grid2Lc/+, suggesting that interneurons are subject to a BAX-dependent target-related death in the Lurcher mutants. Furthermore, electron microscopy showed the normal ultrastructural aspect of a number of parallel fibers in the molecular layer of the Grid2Lc/+; Bax(-/-) double mutant mice and preserved their numerous synaptic contacts on interneurons, suggesting that interneurons could play a trophic role for axon terminals of surviving granule cells. Finally, parallel fibers varicosities in the double mutant established "pseudo-synapses" on glia as well as displayed autophagic profiles, suggesting that the connections established by the parallel fibers in the absence of their Purkinje cell targets were subject to a high turnover involving autophagy.The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target-related death of 90% of the granule cells and 60-75% of the olivary neurons. Inactivation of Bax, a pro-apoptotic gene of the Bcl-2 family, in heterozygous Lurcher mutants (Grid2Lc/+) rescues approximately 60% of the granule cells, but does not rescue Purkinje or olivary neurons. Given the larger size of the cerebellar molecular layer in Grid2Lc/+;Bax(-/-) double mutants compared to Grid2Lc/+ mutants, we analyzed the survival of the stellate and basket interneurons as well as the synaptic connectivity of parallel fibers originating from the surviving granule cells in the absence of their Purkinje cell targets in the Grid2Lc/+;Bax(-/-) cerebellum. Quantification showed a significantly higher density of interneurons ( approximately 60%) in the molecular layer of the Grid2Lc/+;Bax(-/-) mice compared to Grid2Lc/+, suggesting that interneurons are subject to a BAX-dependent target-related death in the Lurcher mutants. Furthermore, electron microscopy showed the normal ultrastructural aspect of a number of parallel fibers in the molecular layer of the Grid2Lc/+; Bax(-/-) double mutant mice and preserved their numerous synaptic contacts on interneurons, suggesting that interneurons could play a trophic role for axon terminals of surviving granule cells. Finally, parallel fibers varicosities in the double mutant established "pseudo-synapses" on glia as well as displayed autophagic profiles, suggesting that the connections established by the parallel fibers in the absence of their Purkinje cell targets were subject to a high turnover involving autophagy.
The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target-related death of 90% of the granule cells and 60-75% of the olivary neurons. Inactivation of Bax, a pro-apoptotic gene of the Bcl-2 family, in heterozygous Lurcher mutants (Grid2Lc/+) rescues approximately 60% of the granule cells, but does not rescue Purkinje or olivary neurons. Given the larger size of the cerebellar molecular layer in Grid2Lc/+;Bax(-/-) double mutants compared to Grid2Lc/+ mutants, we analyzed the survival of the stellate and basket interneurons as well as the synaptic connectivity of parallel fibers originating from the surviving granule cells in the absence of their Purkinje cell targets in the Grid2Lc/+;Bax(-/-) cerebellum. Quantification showed a significantly higher density of interneurons ( approximately 60%) in the molecular layer of the Grid2Lc/+;Bax(-/-) mice compared to Grid2Lc/+, suggesting that interneurons are subject to a BAX-dependent target-related death in the Lurcher mutants. Furthermore, electron microscopy showed the normal ultrastructural aspect of a number of parallel fibers in the molecular layer of the Grid2Lc/+; Bax(-/-) double mutant mice and preserved their numerous synaptic contacts on interneurons, suggesting that interneurons could play a trophic role for axon terminals of surviving granule cells. Finally, parallel fibers varicosities in the double mutant established "pseudo-synapses" on glia as well as displayed autophagic profiles, suggesting that the connections established by the parallel fibers in the absence of their Purkinje cell targets were subject to a high turnover involving autophagy.
Author Vogel, Michael W.
Haeberlé, Anne-Marie
Mariani, Jean
Zanjani, S. Hadi
Selimi, Fekrije
Boeuf, Julien
Bailly, Yannick J.
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1993; 156
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SSID ssj0009938
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Snippet The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target‐related death of 90% of the...
The Lurcher mutation in the Grid2 gene causes the cell autonomous death of virtually all cerebellar Purkinje cells and the target-related death of 90% of the...
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wiley
istex
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SubjectTerms Animals
Apoptosis - genetics
autophagy
Autophagy - genetics
bcl-2-Associated X Protein - genetics
Cell Communication - genetics
Cell Count
Cell Differentiation - genetics
Cell Proliferation
Cell Survival - genetics
Cerebellar Cortex - abnormalities
Cerebellar Cortex - cytology
Cerebellar Cortex - metabolism
cerebellum
Female
Gene Expression Regulation, Developmental - genetics
interneuron
Interneurons - metabolism
Interneurons - secretion
Interneurons - ultrastructure
Male
Mice
Mice, Knockout
Mice, Neurologic Mutants
Microscopy, Electron, Transmission
Nerve Growth Factors - metabolism
Nerve Growth Factors - secretion
Neuroglia - metabolism
Neuroglia - ultrastructure
neuronal death
Purkinje Cells - metabolism
Purkinje Cells - ultrastructure
Receptors, Glutamate - genetics
synapse
Synapses - metabolism
Synapses - ultrastructure
Up-Regulation - genetics
Title Survival of interneurons and parallel fiber synapses in a cerebellar cortex deprived of Purkinje cells: Studies in the double mutant mouse Grid2Lc/+;Bax
URI https://api.istex.fr/ark:/67375/WNG-N7WC2WVF-K/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcne.21017
https://www.ncbi.nlm.nih.gov/pubmed/16739195
https://www.proquest.com/docview/68048222
Volume 497
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