Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 12 de 12
Filter
Add more filters










Publication year range
1.
SLAS Discov ; 25(5): 434-446, 2020 06.
Article in English | MEDLINE | ID: mdl-32292096

ABSTRACT

The voltage-gated sodium channel Nav1.7 is a genetically validated target for pain; pharmacological blockers are promising as a new class of nonaddictive therapeutics. The search for Nav1.7 subtype selective inhibitors requires a reliable, scalable, and sensitive assay. Previously, we developed an all-optical electrophysiology (Optopatch) Spiking HEK platform to study activity-dependent modulation of Nav1.7 in a format compatible with high-throughput screening. In this study, we benchmarked the Optopatch Spiking HEK assay with an existing validated automated electrophysiology assay on the IonWorks Barracuda (IWB) platform. In a pilot screen of 3520 compounds, which included compound plates from a random library as well as compound plates enriched for Nav1.7 inhibitors, the Optopatch Spiking HEK assay identified 174 hits, of which 143 were confirmed by IWB. The Optopatch Spiking HEK assay maintained the high reliability afforded by traditional fluorescent assays and further demonstrated comparable sensitivity to IWB measurements. We speculate that the Optopatch assay could provide an affordable high-throughput screening platform to identify novel Nav1.7 subtype selective inhibitors with diverse mechanisms of action, if coupled with a multiwell parallel optogenetic recording instrument.


Subject(s)
High-Throughput Screening Assays , NAV1.7 Voltage-Gated Sodium Channel/drug effects , Patch-Clamp Techniques , Voltage-Gated Sodium Channel Blockers/isolation & purification , Animals , CHO Cells , Cricetulus , Electrophysiological Phenomena , Electrophysiology , HEK293 Cells , Humans , NAV1.7 Voltage-Gated Sodium Channel/genetics
2.
Drug Discov Today Technol ; 23: 17-25, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28647082

ABSTRACT

There is a pressing need for new and more effective treatments for central nervous system (CNS) disorders. A large body of evidence now suggests that alterations in synaptic transmission and neuronal excitability represent underlying factors for many neurological and psychiatric diseases. However, it has been challenging to target these complex functional domains for therapeutic discovery using traditional neuronal assay methods. Here we review advances in neuronal screening technologies and cellular model systems that enable phenotypic screening of neuronal function as a basis for novel CNS drug discovery approaches.


Subject(s)
Central Nervous System Agents/pharmacology , Central Nervous System Diseases/drug therapy , Drug Discovery , Neurons/drug effects , Cells, Cultured , Central Nervous System Agents/therapeutic use , Central Nervous System Diseases/pathology , Electrodes , High-Throughput Screening Assays , Humans , Induced Pluripotent Stem Cells
3.
Cell Rep ; 16(10): 2711-2722, 2016 09 06.
Article in English | MEDLINE | ID: mdl-27568566

ABSTRACT

Synaptic scaling is a form of homeostatic plasticity driven by transcription-dependent changes in AMPA-type glutamate receptor (AMPAR) trafficking. To uncover the pathways involved, we performed a cell-type-specific screen for transcripts persistently altered during scaling, which identified the µ subunit (µ3A) of the adaptor protein complex AP-3A. Synaptic scaling increased µ3A (but not other AP-3 subunits) in pyramidal neurons and redistributed dendritic µ3A and AMPAR to recycling endosomes (REs). Knockdown of µ3A prevented synaptic scaling and this redistribution, while overexpression (OE) of full-length µ3A or a truncated µ3A that cannot interact with the AP-3A complex was sufficient to drive AMPAR to REs. Finally, OE of µ3A acted synergistically with GRIP1 to recruit AMPAR to the dendritic membrane. These data suggest that excess µ3A acts independently of the AP-3A complex to reroute AMPAR to RE, generating a reservoir of receptors essential for the regulated recruitment to the synaptic membrane during scaling up.


Subject(s)
Adaptor Protein Complex 3/metabolism , Adaptor Protein Complex mu Subunits/metabolism , Endosomes/metabolism , Homeostasis , Neuronal Plasticity/physiology , Receptors, AMPA/metabolism , Up-Regulation , Adaptor Proteins, Signal Transducing/metabolism , Animals , Dendrites/metabolism , Discs Large Homolog 1 Protein/metabolism , Endocytosis , Gene Knockdown Techniques , Mice , Nerve Tissue Proteins/metabolism , Pyramidal Cells/metabolism , Synapses/metabolism , Transcriptome/genetics
4.
J Neurosci ; 34(38): 12877-83, 2014 Sep 17.
Article in English | MEDLINE | ID: mdl-25232122

ABSTRACT

Mutations in methyl-CpG-binding protein 2 (MeCP2) cause Rett syndrome and related autism spectrum disorders (Amir et al., 1999). MeCP2 is believed to be required for proper regulation of brain gene expression, but prior microarray studies in Mecp2 knock-out mice using brain tissue homogenates have revealed only subtle changes in gene expression (Tudor et al., 2002; Nuber et al., 2005; Jordan et al., 2007; Chahrour et al., 2008). Here, by profiling discrete subtypes of neurons we uncovered more dramatic effects of MeCP2 on gene expression, overcoming the "dilution problem" associated with assaying homogenates of complex tissues. The results reveal misregulation of genes involved in neuronal connectivity and communication. Importantly, genes upregulated following loss of MeCP2 are biased toward longer genes but this is not true for downregulated genes, suggesting MeCP2 may selectively repress long genes. Because genes involved in neuronal connectivity and communication, such as cell adhesion and cell-cell signaling genes, are enriched among longer genes, their misregulation following loss of MeCP2 suggests a possible etiology for altered circuit function in Rett syndrome.


Subject(s)
Down-Regulation/genetics , Methyl-CpG-Binding Protein 2/metabolism , Neurons/metabolism , Animals , Cell Adhesion/genetics , Cell Communication/genetics , Disease Models, Animal , Gene Expression Profiling , Male , Mice , Mice, Knockout , Mice, Transgenic , Oligonucleotide Array Sequence Analysis , Organ Specificity , Rett Syndrome/genetics
5.
J Neurosci ; 33(27): 10938-49, 2013 Jul 03.
Article in English | MEDLINE | ID: mdl-23825400

ABSTRACT

Working memory is an essential component of higher cognitive function, and its impairment is a core symptom of multiple CNS disorders, including schizophrenia. Neuronal mechanisms supporting working memory under normal conditions have been described and include persistent, high-frequency activity of prefrontal cortical neurons. However, little is known about the molecular and cellular basis of working memory dysfunction in the context of neuropsychiatric disorders. To elucidate synaptic and neuronal mechanisms of working memory dysfunction, we have performed a comprehensive analysis of a mouse model of schizophrenia, the forebrain-specific calcineurin knock-out mouse. Biochemical analyses of cortical tissue from these mice revealed a pronounced hyperphosphorylation of synaptic vesicle cycling proteins known to be necessary for high-frequency synaptic transmission. Examination of the synaptic vesicle cycle in calcineurin-deficient neurons demonstrated an impairment of vesicle release enhancement during periods of intense stimulation. Moreover, brain slice and in vivo electrophysiological analyses showed that loss of calcineurin leads to a gene dose-dependent disruption of high-frequency synaptic transmission and network activity in the PFC, correlating with selective working memory impairment. Finally, we showed that levels of dynamin I, a key presynaptic protein and calcineurin substrate, are significantly reduced in prefrontal cortical samples from schizophrenia patients, extending the disease relevance of our findings. Our data provide support for a model in which impaired synaptic vesicle cycling represents a critical node for disease pathologies underlying the cognitive deficits in schizophrenia.


Subject(s)
Calcineurin/deficiency , Memory Disorders/metabolism , Memory, Short-Term/physiology , Prefrontal Cortex/metabolism , Synaptic Transmission/physiology , Synaptic Vesicles/metabolism , Adult , Animals , Calcineurin/genetics , Female , Humans , Male , Memory Disorders/genetics , Mice , Mice, Knockout , Middle Aged , Nerve Net/metabolism , Organ Culture Techniques , Synaptic Vesicles/genetics
6.
PLoS One ; 6(10): e25999, 2011.
Article in English | MEDLINE | ID: mdl-21998743

ABSTRACT

Unbiased, high-throughput screening has proven invaluable for dissecting complex biological processes. Application of this general approach to synaptic function would have a major impact on neuroscience research and drug discovery. However, existing techniques for studying synaptic physiology are labor intensive and low-throughput. Here, we describe a new high-throughput technology for performing assays of synaptic function in primary neurons cultured in microtiter plates. We show that this system can perform 96 synaptic vesicle cycling assays in parallel with high sensitivity, precision, uniformity, and reproducibility and can detect modulators of presynaptic function. By screening libraries of pharmacologically defined compounds on rat forebrain cultures, we have used this system to identify novel effects of compounds on specific aspects of presynaptic function. As a system for unbiased compound as well as genomic screening, this technology has significant applications for basic neuroscience research and for the discovery of novel, mechanism-based treatments for central nervous system disorders.


Subject(s)
High-Throughput Screening Assays/methods , Synapses/drug effects , Synapses/physiology , Animals , Cells, Cultured , Drug Discovery , Neurons/cytology , Neurons/drug effects , Rats , Synaptic Vesicles/drug effects , Time Factors
7.
J Neurosci ; 29(21): 7040-52, 2009 May 27.
Article in English | MEDLINE | ID: mdl-19474331

ABSTRACT

Fast-spiking (FS) interneurons are important elements of neocortical circuitry that constitute the primary source of synaptic inhibition in adult cortex and impart temporal organization on ongoing cortical activity. The highly specialized intrinsic membrane and firing properties that allow cortical FS interneurons to perform these functions are attributable to equally specialized gene expression, which is ultimately coordinated by cell-type-specific transcriptional regulation. Although embryonic transcriptional events govern the initial steps of cell-type specification in most cortical interneurons, including FS cells, the electrophysiological properties that distinguish adult cortical cell types emerge relatively late in postnatal development, and the transcriptional events that drive this maturational process are not known. To address this, we used mouse whole-genome microarrays and whole-cell patch clamp to characterize the transcriptional and electrophysiological maturation of cortical FS interneurons between postnatal day 7 (P7) and P40. We found that the intrinsic and synaptic physiology of FS cells undergoes profound regulation over the first 4 postnatal weeks and that these changes are correlated with primarily monotonic but bidirectional transcriptional regulation of thousands of genes belonging to multiple functional classes. Using our microarray screen as a guide, we discovered that upregulation of two-pore K(+) leak channels between P10 and P25 contributes to one of the major differences between the intrinsic membrane properties of immature and adult FS cells and found a number of other candidate genes that likely confer cell-type specificity on mature FS cells.


Subject(s)
Action Potentials/physiology , Gene Regulatory Networks/physiology , Interneurons/physiology , Neocortex/cytology , Neocortex/growth & development , gamma-Aminobutyric Acid/metabolism , Action Potentials/drug effects , Age Factors , Analysis of Variance , Animals , Animals, Newborn , Biophysics , Electric Stimulation , Excitatory Amino Acid Antagonists/pharmacology , Flow Cytometry/methods , Gene Expression Regulation, Developmental/drug effects , Gene Expression Regulation, Developmental/physiology , Gene Regulatory Networks/drug effects , Glutamate Decarboxylase/genetics , Green Fluorescent Proteins/genetics , Inhibitory Postsynaptic Potentials/drug effects , Inhibitory Postsynaptic Potentials/genetics , Interneurons/classification , Interneurons/drug effects , Ion Channels/genetics , Ion Channels/metabolism , Lysine/analogs & derivatives , Lysine/metabolism , Mice , Mice, Transgenic , Microarray Analysis/methods , Patch-Clamp Techniques
8.
Nat Protoc ; 2(11): 2924-9, 2007.
Article in English | MEDLINE | ID: mdl-18007629

ABSTRACT

Sorting of fluorescent cells is a powerful technique for revealing the cellular processes that differ among the various cell types found in complex tissues. With the recent availability of transgenic mouse strains in which specific subpopulations of neurons are labeled, it has become desirable to purify these fluorescent neurons from their surrounding hetereogeneous brain tissue for electrophysiological, biochemical and molecular analyses. This has been accomplished using automated fluorescence-activated cell sorting (FACS) and laser capture microdissection (LCM). Although these procedures can be effective, they have some serious disadvantages, including high equipment costs and difficulty in obtaining samples completely free of contaminating tissue. Here we offer an alternative protocol for purifying fluorescent neurons, which relies on less-expensive equipment, readily produces perfectly pure samples and can be applied to neurons that are only dimly labeled and present in low numbers. The entire protocol can be completed in 3-5 h.


Subject(s)
Brain/cytology , Cell Separation/methods , Fluorescent Dyes/analysis , Neurons/cytology , Animals , Mice , Mice, Transgenic , Microdissection , Microtomy
10.
Trends Neurosci ; 29(6): 339-45, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16714064

ABSTRACT

Neural circuits within the vertebrate brain are composed of highly diverse cell types. The exact extent of this diversity is a matter of continuing debate. For example, do cortical interneurons comprise a few, dozens or >100 distinct cell types? Recently, several groups have used microarrays to measure genome-wide gene expression profiles for specific neuronal cell types. These methods can offer an objective basis for neuronal classification. In this review, we argue that this approach should now be carried out more broadly and that it should be coupled to large-scale efforts to generate mouse driver lines in which tools for genetic manipulation, such as the Cre recombinase, are expressed in identified cell types within the brain. This would enable neuroscientists to begin to investigate more systematically the roles of specific genes in establishing particular cellular phenotypes, and also the roles of particular cell types within brain circuits. This review is part of the TINS special issue on The Neural Substrates of Cognition.


Subject(s)
Brain/cytology , Genomics , Neurons/classification , Neurons/physiology , Animals , Gene Expression Profiling , Humans , Nerve Net/cytology , Nerve Net/physiology
11.
Nat Neurosci ; 9(1): 99-107, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16369481

ABSTRACT

Identifying the neuronal cell types that comprise the mammalian forebrain is a central unsolved problem in neuroscience. Global gene expression profiles offer a potentially unbiased way to assess functional relationships between neurons. Here, we carried out microarray analysis of 12 populations of neurons in the adult mouse forebrain. Five of these populations were chosen from cingulate cortex and included several subtypes of GABAergic interneurons and pyramidal neurons. The remaining seven were derived from the somatosensory cortex, hippocampus, amygdala and thalamus. Using these expression profiles, we were able to construct a taxonomic tree that reflected the expected major relationships between these populations, such as the distinction between cortical interneurons and projection neurons. The taxonomic tree indicated highly heterogeneous gene expression even within a single region. This dataset should be useful for the classification of unknown neuronal subtypes, the investigation of specifically expressed genes and the genetic manipulation of specific neuronal circuit elements.


Subject(s)
Gene Expression/physiology , Neurons/classification , Neurons/ultrastructure , Prosencephalon/cytology , Animals , Bacterial Proteins/genetics , Brain Chemistry/genetics , Data Interpretation, Statistical , Electrophysiology , Flow Cytometry , Fluorescent Dyes , Genes, Reporter/genetics , Green Fluorescent Proteins/genetics , Immunohistochemistry , In Situ Hybridization , Luminescent Proteins/genetics , Male , Mice , Mice, Transgenic , Oligonucleotide Array Sequence Analysis , Patch-Clamp Techniques , Prosencephalon/metabolism , Reverse Transcriptase Polymerase Chain Reaction
12.
J Neurosci Methods ; 120(2): 121-9, 2002 Oct 30.
Article in English | MEDLINE | ID: mdl-12385762

ABSTRACT

We describe the ongoing development of a method that combines multi-unit extracellular recording with intracellular recording to probe unitary synaptic connections in the central nervous system. In multi-unit spike-triggered averaging (multi-unit STA), intracellular recordings are averaged based on extracellularly recorded action potentials from multiple units to rapidly screen large numbers of neuronal pairs for rare synaptic connections. High throughput is achieved by using many extracellular electrodes and online, automated analysis. Using this approach, we were able to screen dozens of candidate pairs per hour. About 1-2% of these were synaptically connected, and for some of these presynaptic unit isolation was sufficient to accurately quantify synaptic properties such as latency, conductance, kinetics and transmission failure rate. Since it requires only a single intracellular recording, multi-unit STA might be a suitable method for probing unitary synaptic connections in the intact brain, where obtaining multiple intracellular recordings is not feasible.


Subject(s)
Electrophysiology/methods , Synapses/physiology , Algorithms , Animals , Electrodes , Electrophysiology/statistics & numerical data , Excitatory Postsynaptic Potentials/physiology , Extracellular Space/physiology , Glutamic Acid/metabolism , Glutamic Acid/physiology , In Vitro Techniques , Membrane Potentials/physiology , Neural Pathways/physiology , Neurons/physiology , Patch-Clamp Techniques , Rats , Rats, Long-Evans , Receptors, Presynaptic/physiology
SELECTION OF CITATIONS
SEARCH DETAIL
...