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Habibollahi, F.

Publications and source records attributed to Habibollahi, F..

6 recordsLinked to original sources

Handwritten Digit classification with neural cultures is influenced by neural architecture, network dynamics, and decoding methods

As silicon-based computing approaches fundamental physical limits, neurocomputing offers an energy-efficient alternative by leveraging the intrinsic non-linear dynamics of biological systems. To harness these dynamics, it is vital to understand the structure-function relationship governing how neural cultures process complex spatio-temporal information and how to appropriately decode the resulting neural electrophysiological activity. We investigated this utilizing a closed-loop electrophysiology platform, the CL1, to implement reservoir computing in human iPSC-derived neuronal networks. To systematically evaluate the variables driving neurocomputational capacity, we explored how cellular composition (cortical vs. hippocampal lineages), and the physical architecture (unstructured monolayers, 3D neural organoids, and modular networks confined by microfluidic devices) influenced electrophysiological properties and interacted with different decoding methodologies. Using a spatio-temporal version of a handwritten digit pattern recognition task (MNIST), we analyzed how these biological and analytical factors influenced classification accuracy. To ensure robust interpretation this required us to first demonstrated that reservoir computing decoding methods require strict artifact control and trial-based cross-validation to distinguish network computation from artifactual signal separability or temporal data leakage. Applying this validated frequency-domain pipeline, we suggest a clear functional hierarchy where structural modularity acts as a vital functional regularizer. Modular cortical cultures significantly outperformed unconstrained monolayers and organoids on MNIST. Furthermore, decoding frequency information from raw signals proved superior to typical time-bin decoding implementations. These findings establish that maximizing the computational potential of Synthetic Biological Intelligence, while avoiding false positives, requires a synergistic optimization of cellular identity, structural governance, and rigorous decoding logic. In doing so, this work provides a critical base establishing the criteria under which to evaluate neurocomputing implementations.

neuroscience↗

A novel protocol for the efficient generation of all three major hippocampal neuronal sub-populations from human pluripotent stem cells

The diverse computational functions of the human hippocampus rely on coordinated interactions among dentate gyrus (DG), CA3, and CA1 subfields, yet generating all three neuronal identities in vitro - particularly CA1 - has remained challenging. Here we establish a reproducible and modular differentiation protocol that directs human pluripotent stem cells (hPSCs) through dorsomedial telencephalic progenitors to yield DG, CA3, and CA1 neuronal subtypes together with hippocampal regionally specified astrocytes. Early tri-inhibition combined with Sonic hedgehog suppression produced dorsal forebrain progenitors (FOXG1+, PAX6+), while FGF2 treatment supported progenitor maintenance and induced TBR2+ intermediate progenitors. Controlled WNT activation using CHIR99021 drove progressive enrichment of PROX1 hippocampal progenitors across two independent donor lines. Terminal differentiation produced MAP2+/TAU+ neurons that expressed DG (PROX1), CA3 (GRIK4), and CA1 (WFS1, OCT6) markers, with maturing synaptic puncta. Defined progenitors generated long-lived (>400 days) hippocampal organoids exhibiting mixed neuronal-glial populations and spontaneous activity characterized by increased firing rates, high information entropy, and hub-like causal connectivity relative to monolayers, whereas astrocytes-supplemented monolayers displayed intermediate maturation. Population level electrophysiological analysis was also conducted to explore the dynamics of these different cultures. This platform enables systematic experimental control over neuron-astrocyte ratios, culture geometry, and developmental timing, providing a foundation for mechanistic studies of human hippocampal development, circuit function, and disease. Note on figure qualityThis is the preprint version of the manuscript. Figures are included adjacent to described results for the convenience of the reader but may be lower resolution due to file size restrictions on bioRxiv. High resolution figures are included as separate .tiff files for download.

neuroscience↗

Drug treatment alters performance in a neural microphysiological system of information processing

Assessment of pharmacological intervention on in vitro neural systems often emphasizes molecular and structural changes. However, neural systems fundamentally process and act on information. For preclinical assays to predict drug efficacy, they must model these physiological functions. DishBrain, an in vitro synthetic biological intelligence (SBI) assay embodying a neural system in a simulated game-world, enables the quantification of this information-processing capacity, however the question remains whether such a system permits classical pharmacological interrogation and dose-response profiling. Hyperactive glutamatergic dysregulation is linked to neurological disorders including epilepsy, and inducible overexpression of neurogenin 2 (NGN2) in human induced pluripotent stem cells (hiPSCs) generates glutamatergic cultures with dysregulated hyperactivity. We therefore tested three anti-seizure medications (ASMs), phenytoin, perampanel, and carbamazepine, on NGN2 neurons from day 21 of differentiation in this system. The key finding was that, while all compounds altered spontaneous firing, carbamazepine 200 {micro}M significantly improved gameplay metrics. This marks the first demonstration of altered SBI following exogenous drug treatment. Notably, only inhibitory compounds enhanced goal-directed activity, linking glutamatergic attenuation to performance. Neurocomputational analysis revealed nuanced pharmacological responses during closed-loop stimulation, highlighting insights beyond spontaneous activity metrics.

neuroscience↗

Human Neural Organoid Microphysiological Systems Show the Building Blocks Necessary for Basic Learning and Memory

Brain Microphysiological Systems including neural organoids derived from human induced pluripotent stem cells offer a unique lens to study the intricate workings of the human brain. This paper investigates the foundational elements of learning and memory in neural organoids, also known as Organoid Intelligence by quantifying immediate early gene expression, synaptic plasticity, neuronal network dynamics, and criticality to demonstrate the utility of these organoids in basic science research. Neural organoids showed synapse formation, glutamatergic and GABAergic receptor expression, immediate early gene expression basally and evoked, functional connectivity, criticality, and synaptic plasticity in response to theta-burst stimulation. In addition, pharmacological interventions on GABAergic and glutamatergic receptors, and input specific theta-burst stimulation further shed light on the capacity of neural organoids to mirror synaptic modulation and short-term potentiation, demonstrating their potential as tools for studying neurophysiological and neurological processes and informing therapeutic strategies for diseases. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=169 SRC="FIGDIR/small/613333v1_ufig1.gif" ALT="Figure 1"> View larger version (54K): org.highwire.dtl.DTLVardef@50a256org.highwire.dtl.DTLVardef@1d1f8c9org.highwire.dtl.DTLVardef@24688borg.highwire.dtl.DTLVardef@4ba3b4_HPS_FORMAT_FIGEXP M_FIG C_FIG Overview of the main components of the experiments conducted. Figure created using BioRender.com.

neuroscience↗

Neural Networks Are Tuned Near Criticality During a Cognitive Task and Distanced from Criticality In a Psychopharmacological Model of Alzheimer's Disease

Dynamical systems exhibit transitions between ordered and disordered states and "criticality" occurs when the system lies at the borderline between these states at which the input is neither strongly damped nor excessively amplified. Impairments in brain function such as dementia or epilepsy could arise from failure of adaptive criticality, and deviation from criticality may be a potential biomarker for cognition-related neurological and psychiatric impairments. Miniscope wide-field calcium imaging of several hundred hippocampal CA1 neurons in freely-behaving mice was studied during rest, a cognitive task of novel object recognition (NOR), and novel object recognition following scopolamine administration that greatly impairs spatial memory encoding. We find that while hippocampal networks exhibit characteristics of a near-critical system at rest, the network activity shifts significantly closer to a critical state when the mice engaged in the NOR task. The dynamics shift away from criticality with impairment of novel object performance due to scopolamine-induced memory impairment. These results support the concept that hippocampal neural networks move closer to criticality when successfully processing increased cognitive load, taking advantage of maximal dynamical range, information content, and transmission that occur in critical regimes.

neuroscience↗

Critical dynamics arise during structured information presentation: analysis of embodied in vitro neuronal networks

AO_SCPLOWBSTRACTC_SCPLOWAmongst the characteristics about information processing in the brain, observations of dynamic near-critical states have generated significant interest. However, theoretical and experimental limitations have precluded a definite answer about when and why neural criticality arises. To explore this topic, we used an in vitro neural network of cortical neurons that was trained to play a simplified game of Pong. We demonstrate that critical dynamics emerge when neural networks receive task-related structured sensory input, reorganizing the system to a near-critical state. Additionally, better task performance correlated with proximity to critical dynamics. However, criticality alone is insufficient for a neuronal network to demonstrate learning in the absence of additional information regarding the consequences of previous actions. These findings have compelling implications for the role of neural criticality.

neuroscience↗