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Pavlinek, A.

Publications and source records attributed to Pavlinek, A..

2 recordsLinked to original sources

A human neuron-microglia tri-culture platform to study the influence of microglia on developing neuronal networks in vitro

Human brain function is dependent on synaptic architecture and function between a range of different cell types. Glutamatergic and GABAergic neurons provide the basis by which the excitatory and inhibitory balance is achieved in cortical networks, and microglia interact with them to shape synaptic architecture and neural networks. Understanding the interactions between these cell types is crucial to elucidating mechanisms relevant to brain physiology and, potentially, to neurodevelopmental and neurological disorders. Here, we establish a rapid and reproducible human tri-culture platform comprising deterministically-programmed glutamatergic neurons, GABAergic neurons, and microglia to facilitate cell-cell interaction studies during human cortical development. Using these deterministically-programmed ioCells, we systematically optimised neuronal ratios, culture conditions, and the timing of microglial integration to generate a stable neuronal network prior to microglia incorporation. Multi-electrode arrays (MEAs) recordings identified an 80:20 glutamatergic-to-GABAergic ratio as the most robust configuration for sustained and reproducible network activity in this context. Structural characterisation using automated high-content imaging confirmed the formation of both excitatory and inhibitory synapses, while longitudinal MEA recordings demonstrated stable network maturation following microglial incorporation. Microglia incorporation influenced neuronal firing dynamics, increasing burst activity without disrupting early synapse formation. As a proof of concept for disease modelling, we incorporated microglia carrying the Alzheimers disease-associated TREM2 R47H mutation and detected subtle but reproducible alterations in neuronal burst dynamics. Together, this work establishes a defined human neuron-microglia triculture platform that enables scalable investigation of neuroimmune interactions and genetic variants, laying the foundations for more complex future models.

neuroscience↗

Electrophysiological development and functional plasticity in dissociated human cerebral organoids across multiple cell lines

Microelectrode arrays (MEAs) are increasingly used to profile the development of synchronised activity in neural organoids, yet no organoid study has investigated the consistency of electrophysiological development across cell lines. Here, we used dissociated neural organoids derived from four cell lines on MEAs to characterise functional synapse development using multiple parameters across time. The dissociated organoids had increasing functional connectivity and network activity over time across all cell lines and plasticity in response to synaptic-like stimulation. Like the organoids they were derived from, dissociated organoid cultures contained a diverse mixture of cell types. Variability in activity parameters was associated with differences in cell type composition and regional identity, which in turn were affected by donor cell line and batch effects. These results demonstrate that dissociated cerebral organoids can generate functional neurons, akin to primary neuronal cultures from brain tissue, providing a scalable model for studies of neurodevelopment and synaptic function.

neuroscience↗