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Izsak, J.

Publications and source records attributed to Izsak, J..

2 recordsLinked to original sources

Non-Physiological Potassium Concentrations in Commercial Culture Media Trigger Acute Epileptiform Activity in Human iPSC-Derived Neurons

Neuronal in vitro cultures are pivotal for studying brain electrophysiological function and dysfunction. Neuronal activity and communication are regulated by extracellular ion concentrations. Therefore, cell culture medium ion concentrations should ideally mimic those of cerebrospinal fluid (CSF) - considered as the milieu for brain cells in vivo. In this study, we demonstrate that commonly used cell culture media, including Neurobasal (+/- A), Neurobasal Plus, and BrainPhys media, do not accurately replicate human CSF ion concentrations. Using human iPSC-derived neuronal networks on microelectrode arrays, we show that the abnormally high potassium concentrations present in all tested cell culture media induce acute epileptiform activity, similar to that elicited by the convulsive drug 4- aminopyridine. These findings raise a critical question: How can human in vitro neuronal activity be defined as physiological and reliably distinguished from pathophysiological activity, if the routinely used ion concentrations in in vitro experiments are causing aberrant neuronal activity? SummaryThe neuronal activity in neuronal in vitro culture relies on extracellular ion concentrations, which should mimic cerebrospinal fluid (CSF). This study shows that common cell culture media and widely used artificial CSF composition in neuroscience research fail to replicate CSF ion levels, causing non-physiological and rather pathological neuronal activity.

neuroscience↗

Ontogeny of oscillatory slow-wave and neuronal population activity in human iPSC-3D cortical circuits

Oscillatory slow-wave activity (0.5--100 Hz) emerges during fetal human cortex development reflecting functional consequences of cellular brain ontogeny. Human induced pluripotent stem cell-derived (iPSC) neural in vitro models recapitulate aspects of in vivo cellular brain ontogeny, while neuronal mesoscale functional ontogeny is largely uncharacterized. We utilized a human iPSC-derived 3D cortical aggregate model to assess properties of emerging oscillatory slow-wave activity and its relation to synchronous neuronal population activity in cortical circuits. We reveal that oscillatory slow-wave activity (< 1 Hz), phased locked to synchronous population bursting, emerges within 14 days in vitro followed by consecutive stages of emerging delta (1--4 Hz), theta (4--11 Hz), beta (11--30 Hz), and gamma (30--55 Hz) oscillatory activity, accompanied by stage-specific changes in neuronal population burst pattern characteristics. We provide a classification of neuronal mesoscale functional ontogeny stages of developing human iPSC-cortical circuits, where each stage is defined by specific oscillatory slow-wave activity and characteristic synchronous neuronal bursting patterns.

neuroscience↗