Access a toolkit of functional, consistent in vitro models to study neurodegenerative disease
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Learn more about ioGlutamatergic Neurons and explore the data
Learn more about ioGlutamatergic Neurons and explore the data
ioGlutamatergic Neurons are ready for experimentation within days post-thaw
ioGlutamatergic Neurons rapidly acquire a homogeneous neuronal phenotype upon thawing, as captured in this 7-day time course. Powered by opti-ox technology, these cells consistently convert to functional excitatory neurons characterised by >80% expression of glutamate transporter genes VGLUT1 and VGLUT2.
Delivered cryopreserved and ready-to-culture, ioGlutamatergic Neurons offer a highly defined, easy-to-use human model for translational research and drug discovery.
opti-ox deterministic cell programming leads to high lot-to-lot consistency in ioGlutamatergic Neurons
Bulk RNA-sequencing analysis of three independent lots of ioGlutamatergic Neurons reveals tight clustering at specific timepoints, demonstrating the manufacturing precision of opti-ox technology. Analysis of differentially expressed genes (|logFC| >0.5 and FDR <0.01) confirms no statistically significant variance between lots, ensuring users can rely on uniform performance and reproducible experimental data across every vial.
Prof. Marius Wernig and Dr. Mark Kotter discuss the paradigm shift of transcription factor-mediated cell programming and how opti-ox technology is industrialising the process. The speakers outline how this approach overcomes traditional variability to enable the scalable, precise manufacturing of human cells.
ioGlutamatergic Neurons display synchronised network activity as early as day 31
Raster plots generated using the capture the rapid development of functional networks in ioGlutamatergic Neurons co-cultured with human iPSC-derived astrocytes. Spontaneous activity observed at day 7 evolves into clear synchronised bursting by day 31, represented by vertical blue lines across 1,024 active electrodes. This confirms a rapidly maturing functional system ideal for assessing network dynamics and compound effects.
ioGABAergic and ioGlutamatergic Neurons form a robust model for studying excitatory-inhibitory neuron imbalances
Co-culturing ioGlutamatergic Neurons, ioGABAergic Neurons, and hiPSC-derived astrocytes provides a physiologically relevant platform to study network hyperexcitability. As shown in the graphs (A) and raster plots (B), ioGABAergic Neurons functionally integrate to inhibit excitatory activity, reducing the number of spikes per network burst in a cell number-dependent manner. This robust multi-cell-culture can be used as a platform to model neurological conditions such as epilepsy, autism and schizophrenia in vitro.
ioGlutamatergic Neurons Alzheimer鈥檚 disease model displays increased amyloid beta secretion
ioGlutamatergic Neurons engineered with the PSEN1 M146L, APP V717I (London) and APP KM670/671NL (Swedish) mutations recapitulate the changes in A尾 peptide ratios observed in Alzheimer鈥檚 disease patients. This demonstrates their validity as an in vitro model to study Alzheimer's disease and for the discovery of drugs targeting the pathogenic A尾 pathway.
ioGlutamatergic Neurons 50CAG/WT demonstrates Huntington鈥檚 disease-related functional deficits
Charles River Laboratories leveraged the MaxTwo HD-MEA system to characterise 糖心原创鈥檚 Huntington鈥檚 disease (HD) model. By comparing ioGlutamatergic Neurons HTT 50CAG/WT to their genetically-matched wild-type control, the team identified distinct functional phenotypes, including delayed network formation, decreased axonal branching, and reduced spontaneous activity. These results demonstrate the model's ability to recapitulate complex disease-related phenotypes, offering a valuable tool for screening.
ioGlutamatergic Neurons provide a robust model for ASO efficacy screening
ioGlutamatergic Neurons demonstrate high suitability for antisense oligonucleotide (ASO) efficacy screening following delivery by gymnosis. The lack of marked intra- or inter-plate variability confirms these cells as a robust, physiologically relevant model for validating therapeutic candidates.
Utilising GFP ioGlutamatergic Neurons for live-cell imaging and easy multi-cell culture tracking
ioGlutamatergic Neurons have been engineered to constitutively express green fluorescent protein (GFP), offering scientists an in vitro, fluorescent human neuronal model ideal for culturing with other cell types, enabling effortless tracking in multi-cellular systems.
Stable GFP expression enables easy, real-time tracking in complex, multi-cellular systems, facilitating the study of glial interactions or network function alongside inhibitory neurons. This makes the cells ideal for live-cell imaging to assess neurite outgrowth, morphology, and survival in response to compound treatment.
CRISPR-Ready ioGlutamatergic Neurons enable CRISPR screening
CRISPRko-Ready ioGlutamatergic Neurons reveal distinct phenotypic clustering in a pooled knockout screen targeting 100 neurodegenerative disease-relevant genes. As visualised in the UMAP, single-cell analysis shows that aminoacyl-tRNA synthetase (aaRS) knockouts鈥攊ncluding AARS1 and GARS1鈥攇roup together, while non-targeting controls remain evenly distributed. Pathway analysis indicates that targeting these genes activates the unfolded protein response (UPR), validating the model's ability to recapitulate mechanisms found in neurodegenerative conditions like Charcot鈥揗arie鈥揟ooth neuropathy (CMT).
Delivered cryopreserved, the cells are ready for experimentation post-thaw
In this video, our scientist takes you through the step-by-step process of how to thaw, seed and culture ioGlutamatergic Neurons, which complements our expert scientist's top tips on understanding the importance of handling cells gently, preparation of coatings, media changes and cell density.
What scientists say about ioGlutamatergic Neurons
Dr Shushant Jain
Group Leader | In Vitro Biology | Charles River, 2021
"These cells enable us to move rapidly as from the moment of plating within 4-7 days we have mature and functional neurons."
Dr Mariangela Iovino
Senior Group Leader | Biology Discovery | Charles River
鈥淥ur major surprise when we first used the ioGlutamatergic Neurons was that after thawing the cells in 384-well format, we could see immediately after 2 days a nice neuronal network, and there was no well to well variability within the same plate. This made our assay quite robust.鈥�
Dr Koby Baranes
Research Associate | University of Cambridge
"These cells provide a reliable and pure source of glutamatergic neurons, resembling primary human ones. They are ready-to-use which makes it much more easy for tissue culture work and for reproducible results.鈥�
Dr Jeremy Anton
Scientist | Charles River
"ioGlutamatergic Neurons are easy to use with a simple application protocol. They recover quickly after thaw and are able to form a mature mesh of neurons ideal for testing within a few days."
Professor Deepak Srivastava
Professor | Molecular Neuroscience | King鈥檚 College London and Group Leader | MRC Centre for Developmental Disorders
"ioGlutamatergic Neurons provide a useful system for studying the effects of IFN-gamma in a pure population of glutamatergic cells"
Build functional excitatory - inhibitory in vitro cultures
Combine defined, consistent glutamatergic and GABAergic neurons
Expand your research
Build functional excitatory - inhibitory in vitro cultures
Combine defined, consistent glutamatergic and GABAergic neurons
Study network synchrony, functional connectivity, and drug responses using MEA in a more physiologically relevant neuronal network with balanced excitatory and inhibitory activity.
Explore ioGABAergic Neurons
Explore ioGABAergic Neuron Disease Models
Simplify functional genomics workflows
Perform gene knockout, activation and interference in iPSC-derived neurons and glia
Expand your research
Simplify functional genomics workflows
Perform gene knockout, activation and interference in iPSC-derived neurons and glia
CRISPR-Ready ioCells stably express Cas9 nuclease or dCas9 variants and come with optimised cell culturing and guide delivery protocols.
Start measuring readouts from gene perturbations and CRISPR screens within days
Explore CRISPR-Ready ioCells
Develop complex multi-cell cultures
Combine ioCells to establish models of inflammation and neurodegeneration
Expand your research
Develop complex multi-cell cultures
Combine ioCells to establish models of inflammation and neurodegeneration
Access our in vitro neuroscience toolkit to develop complex models for investigating cellular communication and disease mechanisms in the human context.
ioMicroglia
ioOligodendrocyte-like cells
ioAstrocytes
Perform controlled and reproducible disease modelling
Access an extensive panel of disease models across different CNS cell types
Expand your research
Perform controlled and reproducible disease modelling
Access an extensive panel of disease models across different CNS cell types
Study the impact of mutations related to neurodegenerative diseases in consistent, defined and scalable human CNS disease model cells with genetically matched controls.
- Alzheimer's disease
- Parkinson's disease
- Huntington's disease
- ALS and FTD
ioGlutamatergic Neurons and disease models user manual | 糖心原创
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CRISPRa-Ready ioGlutamatergic Neurons user manual | 糖心原创
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CRISPRi-Ready ioGlutamatergic Neurons user manual | 糖心原创
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Preparing Culture Vessels for Glutamatergic Neurons | How-to Video
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How to culture ioGlutamatergic Neurons
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mRNA transfection of ioGlutamatergic Neurons | 糖心原创
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Co-culturing ioMicroglia and ioGlutamatergic Neurons | 糖心原创
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Lentiviral transduction of ioGlutamatergic Neurons | 糖心原创
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ioGlutamatergic Neurons ICC staining protocol | 糖心原创
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Co-culturing ioGlutamatergic Neurons with astrocytes for MEA assays | 糖心原创
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Co-culturing ioOligodendrocyte-like cells and ioGlutamatergic Neurons | 糖心原创
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Co-culturing ioGlutamatergic Neurons and ioAstrocytes | 糖心原创
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Developing next-generation in vitro phenotypic assays for Huntington鈥檚 disease by combining a precision reprogrammed hiPSC-derived disease model with high-density microelectrode arrays
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Sartorius application note - Advanced in vitro Modeling of Human iPSC-derived Neuronal Mono- and Co-cultures with Microglia
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Producing 3D Neuronal Microtissues for Preclinical Drug Screening using ioGlutamatergic Neurons
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Generating publishable neuroscience research in 12 weeks with ioGlutamatergic Neurons
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ioGlutamatergic Neurons
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High Content Analysis of 2D and 3D cellular models for target and phenotypic drug discovery
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Genotype and phenotype validation of an isogenic human iPSC-derived neuronal model of Huntington鈥檚 Disease
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Rapid and consistent generation of functional microglia from reprogrammed hiPSCs to study neurodegeneration and neuroinflammation
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Generation and characterisation of a panel of human iPSC-derived neurons and microglia carrying early and late onset relevant mutations for Alzheimer鈥檚 disease
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Alzheimer鈥檚 disease models in iPSC-derived glutamatergic neurons show increased secretion of pathogenic amyloid beta peptides
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Amyloid-beta induces toxicity and cell death in human iPSC-derived neurons: alzheimer disease in vitro model
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An in vitro toolkit to study the cell-specific roles of glutamatergic neurons and glia in Alzheimer鈥檚 disease
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An iPSC-derived neuroinflammation/neurotoxicity in vitro model of neurons and glial cells
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Characterization of a human iPSC derived Huntington鈥檚 disease cell line suitable for disease modelling and drug screening
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Driving experimental reproducibility and lot-to-lot biological consistency in human iPSC-derived cells enabled by opti-ox technology
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Establishment and validation of an in vitro co-culture model to study myelination using human iPSC-derived glutamatergic neurons and oligodendrocytes
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Harnessing CRISPR-Ready ioCells as functional genomics tools for drug target identification and validation
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Modelling neurodegeneration using a human genetically matched system: a next generation approach to study frontotemporal dementia and amyotrophic lateral sclerosis
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Physiologically relevant media unmasks severe mitochondrial dysfunction in a precision reprogrammed iPSC-derived model of Huntington's disease
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Scalable and well defined human glutamatergic and gabaergic co-culture platform for studying excitatory-inhibitory neuron imbalances and the discovery of drugs to treat associated diseases
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Identification of neuronal subtype-specific splice variants in iPSC-derived cell models of ALS and FTD
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iPSC-derived Alzheimer's disease models show increased secretion of pathogenic amyloid beta peptides in glutamatergic neurons and responses to amyloid beta 42 in microglia
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Optimisation of mRNA delivery to overcome transfection challenges in hiPSC-derived neurons and microglia
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opti-ox deterministic cell programming to enable the industrialisation of New Approach Methodologies
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Lipid-Bilayer-Supported 3D Printing of Human Cerebral Cortex Cells Reveals Developmental Interactions
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Reprogramming the stem cell for a new generation of cures
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Inducible and Deterministic Forward Programming of Human Pluripotent Stem Cells into Neurons, Skeletal Myocytes, and Oligodendrocytes
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Compounds co-targeting kinases in axon regulatory pathways promote regeneration and behavioral recovery after spinal cord injury in mice
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Glutamatergic Neurons and Brain Cyst Formation
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Interferon-纬 exposure of human iPSC-derived neurons alters major histocompatibility complex I and synapsin protein expression
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3D bioprinting of iPSC neuron-astrocyte coculture
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Rewiring of the promoter-enhancer interactome and regulatory landscape in glioblastoma orchestrates gene expression underlying neurogliomal synaptic communication
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HNRNPH1 regulates the neuroprotective cold鈥恠hock protein RBM3 expression through poison exon exclusion
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Schizophrenia risk gene ZNF804A controls ribosome localization and synaptogenesis in developing human neurons
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Circadian clocks in human cerebral organoids
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Dynein and dynactin move long-range but are delivered separately to the axon tip
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Drug treatment alters performance in a neural microphysiological system of information processing
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A triple serine motif in the intracellular domain of SorCS2 impacts its cellular signaling
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Phenotypic screening with primary and human iPSC-derived neurons
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Cell-Type Specific Molecular and Functional Consequences of TDP-43 Loss-of-Function in Human Induced Neurons
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NRN1 as a therapeutic target for Alzheimer's disease
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Consistent and scalable human iPSC-derived cells for in vitro disease modelling and drug discovery
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Industrialising Cellular Reprogramming: Leveraging opti-ox Technology to Manufacture Human Cells with Unprecedented Consistency
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In Vitro Approaches to Neurodegeneration: Characterisation of ioGlutamatergic Neurons as PD models
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rAAV meets ioNeurons: Pioneering the future of translational neurotherapies
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Partnering with Charles River to advance CNS drug discovery with ioGlutamatergic Neurons
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In Conversation with Charles River
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Modelling neurodevelopment | Investigating the impact of maternal immune activation on neurodevelopment using human iPSC-derived cells | 糖心原创
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Rethinking Developmental Biology With Cellular Reprogramming | 糖心原创
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Addressing the Reproducibility Crisis | Driving Genome-Wide Consistency in Cellular Reprogramming | 糖心原创
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Running Large-Scale CRISPR Screens in Human Neurons | 糖心原创
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Human iPSC-Based Models of Glial Cells for Studying Neurodegenerative Disease | 糖心原创
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