Name: modeling neuronal death and degeneration in mouse primary cerebellar granule neurons
Uploaded: 2017-11-06T16:30:00
Description: Watch this Scientific Journal Video about Modeling Neuronal Death and Degeneration in Mouse Primary Cerebellar Granule Neurons Video at JoVE.com

This work is supported by Natural Sciences and Engineering Research Council of Canada and the Canadian Institutes of Health Research grants to A.J.-A.

This protocol is based on modifications of procedures that have been described previously 18,24,25,26,27. This protocol is approved by the Animal Care Committee at McGill University.
1. Experimental Preparation
NOTE: The following stock solutions can be prepared and maintained until use.
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	<li>Goldowitz, D., Hamre, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+cells+and+molecules+that+make+a+cerebellum.">The cells and molecules that make a cerebellum.</a> Trends in Neurosciences. 21 (9), 375-382 (1998).</li><li>Contestabile, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cerebellar+granule+cells+as+a+model+to+study+mechanisms+of+neuronal+apoptosis+or+survival+in+vivo+and+in+vitro.">Cerebellar granule cells as a model to study mechanisms of neuronal apoptosis or survival in vivo and in vitro.</a> Cerebellum. 1 (1), 41-55 (2002).</li><li>Bilimoria, P. M., Bonni, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cultures+of+cerebellar+granule+neurons.">Cultures of cerebellar granule neurons.</a> CSH Protoc. , (2008).</li><li>Kramer, D., Minichiello, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cell+culture+of+primary+cerebellar+granule+cells.">Cell culture of primary cerebellar granule cells.</a> Methods Mol Biol. 633, 233-239 (2010).</li><li>Burgoyne, R. D., Cambray-Deakin, M. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+cellular+neurobiology+of+neuronal+development:+the+cerebellar+granule+cell.">The cellular neurobiology of neuronal development: the cerebellar granule cell.</a> Brain Res. 472 (1), 77-101 (1988).</li><li>Hatten, M. E., Heintz, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mechanisms+of+neural+patterning+and+specification+in+the+developing+cerebellum.">Mechanisms of neural patterning and specification in the developing cerebellum.</a> Annu Rev Neurosci. 18, 385-408 (1995).</li><li>Evans, G. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synaptic+signalling+in+cerebellar+plasticity.">Synaptic signalling in cerebellar plasticity.</a> Biol Cell. 99 (7), 363-378 (2007).</li><li>Hunt, D. L., Castillo, P. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synaptic+plasticity+of+NMDA+receptors:+mechanisms+and+functional+implications.">Synaptic plasticity of NMDA receptors: mechanisms and functional implications.</a> Curr Opin Neurobiol. 22 (3), 496-508 (2012).</li><li>Arundine, M., Tymianski, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Molecular+mechanisms+of+calcium-dependent+neurodegeneration+in+excitotoxicity.">Molecular mechanisms of calcium-dependent neurodegeneration in excitotoxicity.</a> Cell Calcium. 34 (4-5), 325-337 (2003).</li><li>Szydlowska, K., Tymianski, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Calcium,+ischemia+and+excitotoxicity.">Calcium, ischemia and excitotoxicity.</a> Cell Calcium. 47 (2), 122-129 (2010).</li><li>Jahani-Asl, A., Germain, M., Slack, R. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mitochondria:+joining+forces+to+thwart+cell+death.">Mitochondria: joining forces to thwart cell death.</a> Biochim Biophys Acta. 1802 (1), 162-166 (2010).</li><li>Rego, A. C., Oliveira, C. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mitochondrial+dysfunction+and+reactive+oxygen+species+in+excitotoxicity+and+apoptosis:+implications+for+the+pathogenesis+of+neurodegenerative+diseases.">Mitochondrial dysfunction and reactive oxygen species in excitotoxicity and apoptosis: implications for the pathogenesis of neurodegenerative diseases.</a> Neurochem Res. 28 (10), 1563-1574 (2003).</li><li>Wei, M. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Proapoptotic+BAX+and+BAK:+a+requisite+gateway+to+mitochondrial+dysfunction+and+death.">Proapoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death.</a> Science. 292 (5517), 727-730 (2001).</li><li>Doyle, K. P., Simon, R. P., Stenzel-Poore, M. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mechanisms+of+ischemic+brain+damage.">Mechanisms of ischemic brain damage.</a> Neuropharmacology. 55 (3), 310-318 (2008).</li><li>Coyle, J. T., Puttfarcken, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Oxidative+stress,+glutamate,+and+neurodegenerative+disorders.">Oxidative stress, glutamate, and neurodegenerative disorders.</a> Science. 262 (5134), 689-695 (1993).</li><li>Cole, K., Perez-Polo, J. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neuronal+trauma+model:+in+search+of+Thanatos.">Neuronal trauma model: in search of Thanatos.</a> Int J Dev Neurosci. 22 (7), 485-496 (2004).</li><li>Cheung, E. C., McBride, H. M., Slack, R. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mitochondrial+dynamics+in+the+regulation+of+neuronal+cell+death.">Mitochondrial dynamics in the regulation of neuronal cell death.</a> Apoptosis. 12 (5), 979-992 (2007).</li><li>Jahani-Asl, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mitofusin+2+protects+cerebellar+granule+neurons+against+injury-induced+cell+death.">Mitofusin 2 protects cerebellar granule neurons against injury-induced cell death.</a> J Biol Chem. 282 (33), 23788-23798 (2007).</li><li>Gallo, V., Kingsbury, A., Balazs, R., Jorgensen, O. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+role+of+depolarization+in+the+survival+and+differentiation+of+cerebellar+granule+cells+in+culture.">The role of depolarization in the survival and differentiation of cerebellar granule cells in culture.</a> J Neurosci. 7 (7), 2203-2213 (1987).</li><li>Miller, T. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Bax+deletion+further+orders+the+cell+death+pathway+in+cerebellar+granule+cells+and+suggests+a+caspase-independent+pathway+to+cell+death.">Bax deletion further orders the cell death pathway in cerebellar granule cells and suggests a caspase-independent pathway to cell death.</a> J Cell Biol. 139 (1), 205-217 (1997).</li><li>Jekabsons, M. B., Nicholls, D. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Bioenergetic+analysis+of+cerebellar+granule+neurons+undergoing+apoptosis+by+potassium/serum+deprivation.">Bioenergetic analysis of cerebellar granule neurons undergoing apoptosis by potassium/serum deprivation.</a> Cell Death Differ. 13 (9), 1595-1610 (2006).</li><li>Piccioli, P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inhibition+of+nuclear+factor-kappaB+activation+induces+apoptosis+in+cerebellar+granule+cells.">Inhibition of nuclear factor-kappaB activation induces apoptosis in cerebellar granule cells.</a> J Neurosci Res. 66 (6), 1064-1073 (2001).</li><li>D'Mello, S. R., Galli, C., Ciotti, T., Calissano, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Induction+of+apoptosis+in+cerebellar+granule+neurons+by+low+potassium:+inhibition+of+death+by+insulin-like+growth+factor+I+and+cAMP.">Induction of apoptosis in cerebellar granule neurons by low potassium: inhibition of death by insulin-like growth factor I and cAMP.</a> Proc Natl Acad Sci U S A. 90 (23), 10989-10993 (1993).</li><li>Gallo, V., Ciotti, M. T., Coletti, A., Aloisi, F., Levi, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Selective+release+of+glutamate+from+cerebellar+granule+cells+differentiating+in+culture.">Selective release of glutamate from cerebellar granule cells differentiating in culture.</a> Proc Natl Acad Sci U S A. 79 (24), 7919-7923 (1982).</li><li>Messer, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+maintenance+and+identification+of+mouse+cerebellar+granule+cells+in+monolayer+culture.">The maintenance and identification of mouse cerebellar granule cells in monolayer culture.</a> Brain Res. 130 (1), 1-12 (1977).</li><li>Jahani-Asl, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CDK5+phosphorylates+DRP1+and+drives+mitochondrial+defects+in+NMDA-induced+neuronal+death.">CDK5 phosphorylates DRP1 and drives mitochondrial defects in NMDA-induced neuronal death.</a> Hum Mol Genet. 24 (16), 4573-4583 (2015).</li><li>Jahani-Asl, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+mitochondrial+inner+membrane+GTPase,+optic+atrophy+1+(Opa1),+restores+mitochondrial+morphology+and+promotes+neuronal+survival+following+excitotoxicity.">The mitochondrial inner membrane GTPase, optic atrophy 1 (Opa1), restores mitochondrial morphology and promotes neuronal survival following excitotoxicity.</a> J Biol Chem. 286 (6), 4772-4782 (2011).</li><li>Li, M., Husic, N., Lin, Y., Snider, B. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Production+of+lentiviral+vectors+for+transducing+cells+from+the+central+nervous+system.">Production of lentiviral vectors for transducing cells from the central nervous system.</a> J Vis Exp. (63), e4031 (2012).</li><li>Wang, X., McManus, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Lentivirus+production.">Lentivirus production.</a> J Vis Exp. (32), (2009).</li><li>Lee, H. Y., Greene, L. A., Mason, C. A., Manzini, M. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Isolation+and+culture+of+post-natal+mouse+cerebellar+granule+neuron+progenitor+cells+and+neurons.">Isolation and culture of post-natal mouse cerebellar granule neuron progenitor cells and neurons.</a> J Vis Exp. (23), (2009).</li><li>Holubowska, A., Mukherjee, C., Vadhvani, M., Stegmuller, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Genetic+manipulation+of+cerebellar+granule+neurons+in+vitro+and+in+vivo+to+study+neuronal+morphology+and+migration.">Genetic manipulation of cerebellar granule neurons in vitro and in vivo to study neuronal morphology and migration.</a> J Vis Exp. (85), (2014).</li></ol>

Here we provide a simple method for the culturing of primary mouse cerebellar granule neurons (CGNs), loss and gain of function studies, and modeling different mechanisms of cell death. Several factors affect the reproducibility of the results using this procedure which require close monitoring. These include the purity of the culture including the elimination of glial cells in the culture, the confluence of the culture, and maintaining healthy cells. Introducing variability in these factors can bias the results and chal...

Cerebellar granule neurons (CGNs) are well characterized in culture and have served as an effective model to study neuronal death and development 1,2,3,4,5,6. The early expression of N-methyl-D-aspartate (NMDA) receptors in CGN cultures in vitro makes them an attractive model to study NMDA-induced signalling. Activation of these receptors with NMDA in conjunction with membrane depolarization is used to model physiological neuronal activity stimulation, and has allowed for research into the mechanisms of synaptic plasticity 7,8. On the contrary, over-stimulation of these receptors by NMDA ligand can be used to model excitotoxicity, a major mechanism of neuronal loss in acute brain damage and neurodegenerative diseases 9. One mechanism for the induction of excitotoxicity is through ATP starvation with reduced oxygen, as seen with acute neuronal injury. This results in membrane depolarization and elevated levels of glutamate release at the synapse. The subsequent overstimulation of the NMDA receptor by elevated glutamate results in excessive Ca2+ influx via these receptors, which in turn activates several pathways including Ca2+-activated proteases, phospholipases, and endonucleases, resulting in the uncontrolled degradation of critical cellular components and cell death. Additionally, high intracellular Ca2+ leads to the generation of oxygen free radicals and mitochondrial damage 10,11.
While the majority of neuronal loss following NMDA-induced neuronal excitotoxicity is due to calcium influx and is Bax/Bak independent, other mechanisms of cell death cannot be excluded from this model. The appearance of both necrotic and apoptotic like cell death due to excitotoxicity is partially due to the generation of reactive oxygen species (ROS) and DNA damage caused by high intracellular Ca2+ levels 12. DNA damage results in neuronal death through apoptotic mechanisms, being correlated with hallmarks of apoptotic cell death, such as the appearance of chromatin masses and apoptotic bodies. Induction of apoptosis is mediated through the release of cytochrome c from the mitochondria, and has been shown to be dependent on Bax/Bak oligomerization 13. Bax/Bak oligomerization promotes pore formation in the outer mitochondrial membrane, resulting in cytochrome c release and the activation of pro-apoptotic regulators as seen with mild ischemic injury 14.
Generation of ROS is a significant issue in the brain due to the low endogenous levels of antioxidants, coupled with the large oxygen requirement for neuronal functioning 15. When exposed to an ischemic event, nitric oxide synthase is upregulated , producing nitric oxide and increasing reactive oxygen species 14. The increased concentration of oxygen radicals can result in DNA damage and indirectly cause energy starvation. High levels of DNA double-stranded breaks are remedied by the activation of poly ADP-ribose polymerase-1 (PARP-1), an eukaryotic chromatin-bound protein responsible for catalyzing the transfer of ADP-ribose units from NAD+, a process integral to DNA repair 16. However, with excessive damage due to oxidative stress, PARP-1 activation can cause energy starvation due to the increased drain on NAD+, a necessary substrate for ATP production through oxidative phosphorylation. Ultimately, oxidative stress will trigger apoptosis in a Bax/Bak dependant manner leading to mitochondrial cytochrome c release, and has been shown to induce mitochondrial remodelling in CGNs 17.
Finally, changes in concentration of potassium chloride (KCl) in CGN cultures can be used to model low potassium/depolarization mediated apoptosis 18,19,20. When exposed to low levels of K+, CGNs undergo distinct physiological changes, resulting in reductions of both mitochondrial respiration and glycolysis, attributed to decreased cellular demand 21, as well as reduction in levels of nuclear factor-&#954;B (NF&#954;B) which regulates activities including inflammation and synaptic transmission 22. This model is of particular interest for the study of cell death during neuronal development. The low K+ environment more closely resembles physiological conditions, and causes hallmarks of cell death seen during neuronal development 23.
In summary, CGNs provide a longstanding model to investigate the underlying molecular mechanisms of neuronal death and degeneration. The following protocol will allow isolation and culturing of CGNs, expression or repression of a particular genetic pathway using viruses and the induction of neuronal death via different mechanisms representing neuronal injury and degeneration.

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			<td height="21" style="height:21px;">Poly D-lysine&#160;</td>
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			<td height="21" style="height:21px;width:333px;">DMEM</td>
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			<td style="width:219px;">#319-005-CL</td>
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			<td height="21" style="height:21px;width:333px;">FBS</td>
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			<td style="width:219px;">#080-450</td>
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modeling neuronal death and degeneration in mouse primary cerebellar granule neurons

Cerebellar granule neurons (CGNs) are a commonly used neuronal model, forming an abundant homogeneous population in the cerebellum. In light of their post-natal development, abundance, and accessibility, CGNs are an ideal model to study neuronal processes, including neuronal development, neuronal migration, and physiological neuronal activity stimulation. In addition, CGN cultures provide an excellent model for studying different modes of cell death including excitotoxicity and apoptosis. Within a week in culture, CGNs express N-methyl-D-aspartate (NMDA) receptors, a specific ionotropic glutamate receptor with many critical functions in neuronal health and disease. The addition of low concentrations of NMDA in conjunction with membrane depolarization to rodent primary CGN cultures has been used to model physiological neuronal activity stimulation while the addition of high concentrations of NMDA can be employed to model excitotoxic neuronal injury. Here, a method of isolation and culturing of CGNs from 6 day old pups as well as genetic manipulation of CGNs by adenoviruses and lentiviruses are described. We also present optimized protocols on how to stimulate NMDA-induced excitotoxicity, low-potassium-induced apoptosis, oxidative stress and DNA damage following transduction of these neurons.

With careful dissection, the intact brain should be removed with minimal damage as seen in Figure 1A-B. Effort should be taken to minimize damage to the brain during removal, particularly damage to the cerebellum. Damaging the cerebellum makes for more difficult identification and complete removal of the meninges, and increases the likelihood of contamination of the neuronal culture. Once the meninges have been removed, the cerebellum can be ...

Watch this Scientific Journal Video about Modeling Neuronal Death and Degeneration in Mouse Primary Cerebellar Granule Neurons Video at JoVE.com

Modeling Neuronal Death and Degeneration in Mouse Primary Cerebellar Granule Neurons Video (Video) | JoVE

This protocol describes a simple method for isolating and culturing primary mouse cerebral granule neurons (CGNs) from 6-7 day old pups, efficient transduction of CGNs for loss and gain of function studies, and modelling NMDA-induced neuronal excitotoxicity, low-potassium-induced cell death, DNA-damage, and oxidative stress using the same culture model.

Modeling Neuronal Death and Degeneration in Mouse Primary Cerebellar Granule Neurons

Cerebellar granule neurons (CGNs) are a commonly used neuronal model, forming an abundant homogeneous population in the cerebellum. In light of their ...

Research

JoVE Journal

Neuroscience

In utero Electroporation followed by Primary Neuronal Culture for Studying Gene Function in Subset of Cortical Neurons

In utero Electroporation followed by Primary Neuronal Culture for Studying Gene Function in Subset of Cortical Neurons (Video) | JoVE 

In vitro study of primary neuronal cultures allows for quantitative analyses of neurite outgrowth. In order to study how genetic alterations affect ...

Nucleofection and Primary Culture of Embryonic Mouse Hippocampal and Cortical Neurons

Nucleofection and Primary Culture of Embryonic Mouse Hippocampal and Cortical Neurons (Video) | JoVE 

Hippocampal and cortical neurons have been used extensively to study central nervous system (CNS) neuronal polarization, axon/dendrite outgrowth, and ...

Quantitative Analysis of Synaptic Vesicle Pool Replenishment in Cultured Cerebellar Granule Neurons using FM Dyes

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After neurotransmitter release in central nerve terminals, SVs are rapidly retrieved by endocytosis.  Retrieved SVs are then refilled with ...

Genetic Manipulation of Cerebellar Granule Neurons In Vitro and In Vivo to Study Neuronal Morphology and Migration

Genetic Manipulation of Cerebellar Granule Neurons In Vitro and In Vivo to Study Neuronal Morphology and Migration Video (Video) | JoVE

Developmental events in the brain including neuronal morphogenesis and migration are highly orchestrated processes. In vitro and in vivo analyses allow ...

Primary Culture of Mouse Dopaminergic Neurons

Primary Culture of Mouse Dopaminergic Neurons Video (Video) | JoVE

Dopaminergic neurons represent less than 1% of the total number of neurons in the brain. This low amount of neurons regulates important brain functions ...

Ex Vivo Imaging of Postnatal Cerebellar Granule Cell Migration Using Confocal Macroscopy

Ex Vivo Imaging of Postnatal Cerebellar Granule Cell Migration Using Confocal Macroscopy Video (Video) | JoVE

During postnatal development, immature granule cells (excitatory interneurons) exhibit tangential migration in the external granular layer, and then ...

Selective Depletion of Microglia from Cerebellar Granule Cell Cultures Using L-leucine Methyl Ester

Selective Depletion of Microglia from Cerebellar Granule Cell Cultures Using L-leucine Methyl Ester Video (Video) | JoVE

Microglia, the resident immunocompetent cells of the CNS, play multifaceted roles in modulating and controlling neuronal function, as well as mediating ...

Assessment of Neuronal Viability Using Fluorescein Diacetate-Propidium Iodide Double Staining in Cerebellar Granule Neuron Culture

Assessment of Neuronal Viability Using Fluorescein Diacetate-Propidium Iodide Double Staining in Cerebellar Granule Neuron Culture Video (Video) | JoVE

Primary cultured Cerebellar Granule Neurons (CGNs) have been widely used as an in vitro model in neuroscience and neuropharmacology research. However, the ...

Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons

Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons Video (Video) | JoVE

Neurodegeneration of spinal motoneurons (MNs) is implicated in a large spectrum of neurological disorders including amyotrophic lateral sclerosis, ...

Ballistic Labeling of Pyramidal Neurons in Brain Slices and in Primary Cell Culture

Ballistic Labeling of Pyramidal Neurons in Brain Slices and in Primary Cell Culture Video (Video) | JoVE

It has been reported that the size and shape of dendritic spines is related to their structural plasticity. To identify the morphological structure of ...