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 in | Journal of comparative neurology (1911) Vol. 497; no. 4; pp. 622 - 635 |
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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. |
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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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References_xml | – reference: Caddy KWT, Biscoe TJ. 1979. Structural and quantitative studies on the normal CH3 and lurcher mutant mouse. Philos Trans R Soc Lond B 287: 167-201. – reference: Sotelo C. 1991. Cerebellar synaptogenesis: mutant mice-neuronal grafting. J Physiol Paris 85: 134-144. – reference: Wetts R, Herrup K. 1982c. Cerebellar Purkinje cells are descended from a small number of progenitors committed during early development. Qualitative analysis of lurcher chimeric mice. J Neurosci 2: 1494-1498. – reference: Wetts R, Herrup K. 1983. Direct correlation between Purkinje and granule cell number in the cerebella of lurcher chimeras and wild-type mice. Dev Brain Res 10: 41-47. – reference: Herrup K, Sunter K. 1987. Numerical matching during cerebellar development : quantitative analysis of granule cell death in staggerer mouse chimeras. J Neurosci 7: 829-836. – reference: Fan H, Favero M, Vogel MW. 2001. 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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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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 |
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