NETRI News.

Development of a high-throughput arrayed neural circuitry platform using human induced neurons for drug screening applications

Abstract Proper brain function relies on the precise arrangement and flow of information between diverse neural subtypes. Developing improved human cell-based models which faithfully mimic biologically relevant connectivity patterns may improve drug screening efforts given the limited success of animal models to predict safety and efficacy of therapeutics in human clinical trials. To address this need, we have developed experimental models of defined neural circuitries through the compartmentalization of neuronal cell subtypes in a 96 well plate-based platform where each microwell is divided into two compartments connected by microchannels allowing high-throughput screening (HTS) of small molecules. We demonstrate that we can generate subtype-specific excitatory and inhibitory induced neuronal cells (iNs) from human stem cell lines and that these neurons form robust functional circuits with defined connectivity. Through the use of the genetically encoded calcium indicator GCaMP6f, we monitor calcium ion transients generated during neuronal firing between and within compartments. We further demonstrate functionality of the circuit by perturbing network activity through the addition of glutamate receptor blockers using automated liquid handling. Lastly, we show that we can stimulate network activity in defined neuronal subtypes through the expression of the designer receptor exclusively activated by designer drugs (DREADD) hM3Dq and application of the ligand clozapine-N-oxide (CNO). Our results demonstrate the formation of functional neural circuits in a high-throughput platform that is compatible with compound screening, representing an important step towards developing new screening platforms for studying and ultimately treating psychiatric brain disorders that arise from disordered neural circuit function. Joseph A. Fantuzzo, Denise A. Robles, Vincent R. Mirabella, Ronald P. Hart, Zhiping P. Pang, Jeffrey D. Zahn. Full texte here

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Deposition chamber technology as building blocks for a standardized brain-on-chip framework

In vitro modeling of human brain connectomes is key to explore the structure-function relationship of the centralnervous system. The comprehension of this intricate relationship will serve to better study the pathological mechanismsof neurodegeneration, and hence to perform improved drug screenings for complex neurological disorders, such asAlzheimer’s and Parkinson’s diseases. However, currently used in vitro modeling technologies lack potential to mimicphysiologically relevant neural structures, because they are unable to represent the concurrent interconnectivitybetween myriad subtypes of neurons across multiple brain regions. Here, we present an innovative microfluidic designthat allows the controlled and uniform deposition of various specialized neuronal populations within unique platingchambers of variable size and shape. By applying our design, we offer novel neuro-engineered microfluidic platforms,so called neurofluidic devices, which can be strategically used as organ-on-a-chip platforms for neuroscience research.Through the fine tuning of the hydrodynamic resistance and the cell deposition rate, the number of neurons seeded ineach plating chamber can be tailored from a thousand up to a million, creating multi-nodal circuits that representconnectomes existing within the intact brain. These advances provide essential enhancements to in vitro platforms inthe quest accurately model the brain for the investigation of human neurodegenerative diseases.

Microfluidic neurite guidance to study structure-function relationships in topologicallycomplex population-based neural networks

ABSTRACT The central nervous system is a dense, layered, 3D interconnected network of populations of neurons,and thus recapitulating that complexity for in vitro CNS models requires methods that can createdefined topologically-complex neuronal networks. Several three-dimensional patterning approacheshave been developed but none have demonstrated the ability to control the connections betweenpopulations of neurons. Here we report a method using AC electrokinetic forces that can guide,accelerate, slow down and push up neurites in un-modified collagen scaffolds. We present a means tocreate in vitro neural networks of arbitrary complexity by using such forces to create 3D intersectionsof primary neuronal populations that are plated in a 2D plane. We report for the first time in vitro basicbrain motifs that have been previously observed in vivo and show that their functional network is highlydecorrelated to their structure. This platform can provide building blocks to reproduce in vitro thecomplexity of neural circuits and provide a minimalistic environment to study the structure-functionrelationship of the brain circuitry. T. Honegger, M. I. Thielen, S. Feizi, N. E. Sanjana, J. Voldman, Sci. Rep. 2016, 6, 28384. Full text here

Electrokinetic confinement of axonal growth for dynamically configurable neural networks

Abstract Axons in the developing nervous system are directed via guidance cues, whose expression varies both spatially and temporally, to create functional neural circuits. Existing methods to create patterns of neural connectivity in vitro use only static geometries, and are unable to dynamically alter the guidance cues imparted on the cells. We introduce the use of AC electrokinetics to dynamically control axonal growth in cultured rat hippocampal neurons. We find that the application of modest voltages at frequencies on the order of 105 Hz can cause developing axons to be stopped adjacent to the electrodes while axons away from the electric fields exhibit uninhibited growth. By switching electrodes on or off, we can reversibly inhibit or permit axon passage across the electrodes. Our models suggest that dielectrophoresis is the causative AC electrokinetic effect. We make use of our dynamic control over axon elongation to create an axon-diode via an axon-lock system that consists of a pair of electrode ‘gates’ that either permit or prevent axons from passing through. Finally, we developed a neural circuit consisting of three populations of neurons, separated by three axon-locks to demonstrate the assembly of a functional, engineered neural network. Action potential recordings demonstrate that the AC electrokinetic effect does not harm axons, and Ca2+ imaging demonstrated the unidirectional nature of the synaptic connections. AC electrokinetic confinement of axonal growth has potential for creating configurable, directional neural networks. T. Honegger, M. A. Scott, M. F. Yanik, J. Voldman, Lab Chip 2013, 13, 589. Full text here

La Région Auvergne-Rhône-Alpes soutient NETRI

La Région Auvergne-Rhône-Alpes a répondu favorablement à NETRI dans le cadre de l’opération « Financement d’une prestation d’accompagnement conseils dans le cadre du dispositif Ambition Innovation – Être accompagné dans mon projet « Industrie future  ».  

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