Biology subjects

Heiney, K.

Publications and source records attributed to Heiney, K..

4 recordsLinked to original sources

bioRxiv2026

Memory consolidation and representational drift

Memory consolidation is the process by which temporary, malleable memories are transformed into more stable, longer-lasting forms. On a coarse anatomical scale, consolidation redistributes memories in the brain, but it remains poorly understood how these changes manifest themselves on the finer, cellular scale of neuronal engrams and how they relate to the cognitive level. In this study, we developed a phenomenological model of engram dynamics under systems consolidation. The model describes consolidation as a brain-wide phenomenon, where memories deterministically follow a trajectory through a space of patterns distributed among brain regions. It captures a broad range of features of memory consolidation, including selective consolidation, semantization, and power-law forgetting. In the model, consolidation is accompanied by population-level changes in neuronal representations that resemble the widely observed phenomenon of representational drift. When only a subset of neurons is observed, the deterministic dynamics of the model can appear stochastic, and a readout of task features deteriorates over time even when a stable readout exists for the full system. Our model offers a dynamical systems perspective on memory consolidation as a distributed process, moving beyond the classic region-centered view, and provides a functional interpretation of drift as a means of redistributing engrams for improved memory retention.

neuroscience↗

bioRxiv2025

Information theoretic measures of neural and behavioural coupling predict representational drift

In many parts of the brain, population tuning to stimuli and behaviour gradually changes over the course of days to weeks in a phenomenon known as representational drift. The tuning stability of individual cells varies over the population, and it remains unclear what drives this heterogeneity. We investigate how a neurons tuning stability relates to its shared variability with other neurons in the population using two published datasets from posterior parietal cortex and visual cortex. We quantified the contribution of pairwise interactions to behaviour or stimulus encoding by partial information decomposition, which breaks down the mutual information between the pairwise neural activity and the external variable into components uniquely provided by each neuron and by their interactions. Information shared by the two neurons is termed redundant, and information requiring knowledge of the state of both neurons is termed synergistic. We found that a neurons tuning stability is positively correlated with the strength of its average pairwise redundancy with the population, and that these high-redundancy neurons also tend to show high average pairwise synergy. We hypothesize that subpopulations of neurons show greater stability because they are tuned to salient features common across multiple tasks. Regardless of the mechanistic implications of our work, the stability-redundancy relationship may support improved longitudinal neural decoding in technology that has to track population dynamics over time, such as brain-machine interfaces. Author summaryActivity in the brain represents information about the outside world and how we interact with it. Recent evidence shows that these representations slowly change day to day, while memories and learned behaviours stay stable. Individual neurons change their relationship to external variables at different rates, and we explore how interactions with other neurons in the population relates to this neuron-to-neuron variability. We find that more stable neurons tend to share information about external variables with many other neurons. Our results suggest there are constraints on how representations can change over time, and that these constraints are exhibited in shared fluctuations in activity among neurons in the population.

neuroscience↗

bioRxiv2020

Criticality as a measure of developing proteinopathy in engineered human neural networks

A patterned spread of proteinopathy represents a common characteristic of many neurodegenerative diseases. In Parkinsons disease (PD), misfolded forms of alpha-synuclein proteins aggregate and accumulate in hallmark pathological inclusions termed Lewy bodies and Lewy neurites, which seems to affect selectively vulnerable neuronal populations and propagate within interconnected neuronal networks. Research findings suggest that these proteinopathic inclusions are present at very early timepoints in disease development, even before strong behavioural symptoms of dysfunction arise, but that these underlying pathologies might be masked by homeostatic processes working to maintain the function of the degenerating neural circuits. This study investigates whether inducing the PD-related alpha-synuclein pathology in engineered human neural networks can be associated with changes in network function, and particularly with network criticality states. Self-organised criticality represents the critical point between resilience against perturbation and adaptational flexibility, which appears to be a functional trait in self-organising neural networks, both in vitro and in vivo. By monitoring the developing neural network activity through the use of multielectrode arrays (MEAs) for a period of three weeks following proteinopathy induction, we show that although this developing pathology is not clearly manifest in standard measurements of network function, it may be discerned by differences in network criticality states.

neuroscience↗

bioRxiv2020

Structural and functional alterations associated with the LRRK2 G2019S mutation revealed in structured human neural networks

Mutations in the LRRK2 gene have been widely linked to Parkinsons disease. The G2019S variant has been shown to contribute uniquely to both familial and sporadic forms of the disease. LRRK2-related mutations have been extensively studied, yet the wide variety of cellular and network events directly or indirectly related to these mutations remain poorly understood. In this study, we structured multi-nodal human neural networks carrying the G2019S mutation using custom-designed microfluidic chips coupled to microelectrode-arrays. By applying live imaging approaches, immunocytochemistry and computational modelling, we have revealed alterations in both the structure and function of the resulting neural networks when compared to controls. We provide first evidence of increased neuritic density associated with the G2019S LRRK2 mutation, while previous studies have found either a strong decrease, or no change, compared to controls. Additionally, we corroborate previous findings regarding increased baseline network activity compared to control neural networks. Furthermore, we can reveal additional network alterations attributable to the specific mutation by selectively inducing transient overexcitation to confined parts of the structured multi-nodal networks. These alterations, which we were able to capture both at the micro- and mesoscale manifested as differences in relative network activity and correlation, as well as in mitochondria activation, neuritic remodelling, and synaptic alterations. Our study thus provides important new insights into early signs of neural network pathology significantly expanding upon the current knowledge relating to the G2019S Parkinsons disease mutation.

neuroscience↗