Publication | Open Access
High-resolution CMOS MEA platform to study neurons at subcellular, cellular, and network levels
337
Citations
46
References
2015
Year
EngineeringCircuit NeuroscienceBiomedical EngineeringSensory SystemsNeurochipSocial SciencesSensory NeuroscienceLow-noise Readout ChannelsNeuromorphic EngineeringParallel AccessNeurocomputersComputer EngineeringNetwork LevelsNeural InterfaceNeural InterfacesNeuroengineeringNeurophysiologyComputational NeuroscienceCellular NeuroscienceNeural CircuitsBiomedical ImagingBioelectronicsBiomedical InstrumentationNeuroscienceBrain ElectrophysiologyCentral Nervous SystemBrain-like ComputingThousand Cells
Neuronal network studies would benefit from simultaneous, parallel access to the activity of a large fraction of all neurons. We present a CMOS-based device capable of simultaneously recording the electrical activity of over a thousand cells in in vitro neuronal networks. The device employs a rapidly reconfigurable array of 26,400 microelectrodes at 17.5 µm pitch, allowing any subset to be connected to 1,024 low‑noise readout channels and 32 stimulation units for simultaneous recording and stimulation. It delivers high spatiotemporal resolution that enables simultaneous subcellular, cellular, and network‑level recordings, and we demonstrate its use in whole‑network recordings and axonal property investigations.
Studies on information processing and learning properties of neuronal networks would benefit from simultaneous and parallel access to the activity of a large fraction of all neurons in such networks. Here, we present a CMOS-based device, capable of simultaneously recording the electrical activity of over a thousand cells in in vitro neuronal networks. The device provides sufficiently high spatiotemporal resolution to enable, at the same time, access to neuronal preparations on subcellular, cellular, and network level. The key feature is a rapidly reconfigurable array of 26 400 microelectrodes arranged at low pitch (17.5 μm) within a large overall sensing area (3.85 × 2.10 mm(2)). An arbitrary subset of the electrodes can be simultaneously connected to 1024 low-noise readout channels as well as 32 stimulation units. Each electrode or electrode subset can be used to electrically stimulate or record the signals of virtually any neuron on the array. We demonstrate the applicability and potential of this device for various different experimental paradigms: large-scale recordings from whole networks of neurons as well as investigations of axonal properties of individual neurons.
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