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Biology subjects

Homer, M.

Publications and source records attributed to Homer, M..

3 recordsLinked to original sources

Next-Generation Neural Mass Models Reproduce Features of Speech Processing

Segregation of speech into syllables is a key step in neural speech processing. It relies on the alignment of neural activity with the rhythmic structure of speech. Two competing hypotheses explain this neural speech tracking, phase-resetting and evoked responses. While phenomenological modelling of these hypotheses has been successful, we still lack understanding of the underlying cortical circuits. To investigate these mechanisms, we evaluate whether a biophysical next-generation neural mass model can reproduce several features of neural speech tracking, using phenomenological models of the competing hypotheses as algorithmic baselines. We investigate the models dynamics with four tests: recreating in-silico an EEG experiment that identified a correlation between tracking strength and phoneme sharpness, computing the Phase Concentration Metric, testing the effect of varying syllabic rates, and evaluating the Inter Event Phase Coherence across phoneme onsets. While all of the models that we study reproduce the sharpness-tuned rhythmic speech tracking, the evoked model requires a pre-processed acoustic edge impulse stimulus. We demonstrate that the neural mass model is performing thresholded phase-resetting triggered by sharp onsets in the continuous speech envelope. This produces cross-frequency nested oscillations that qualitatively match an experimentally-observed dual-peak signature in the Inter Event Phase Coherence. Our results indicate that the biophysical neural mass model provides a mechanistic bridge between generic oscillatory dynamics in cortical populations and the cognitive computations of speech tracking. Indeed, the non-linear dynamics of the neural mass model offer an explanation for how peak-rate event representations in auditory cortex activity arise in response to continuous acoustic input. Significance StatementSyllable segregation is crucial but challenging as natural speech lacks clear boundaries, yet humans perform this computation effortlessly. Speech aligns neural activity to syllabic rhythms, predicting syllable timing, but the underlying cortical mechanisms remain unknown. Relating this macroscopic behaviour to neurobiology is challenging; however, next-generation neural mass models promise to resolve this. We demonstrate that these models reproduce sharpness-tuned tracking and acoustic edge extraction. Dynamical analyses indicate this occurs through thresholded phase-resetting to phoneme onsets, triggering cross-frequency nested oscillations. Our results both advance biophysical understanding of syllable segregation and validate the models capacity for simulating macroscopic neural activity. These models offer a bridge between the neurobiology of the auditory cortex and speech processing dynamics that phenomenological models cannot provide.

neuroscience↗

In-silico and in-vitro morphometric analysis of intestinal organoids

Organoids offer a powerful model to study cellular self-organisation, the growth of specific tissue morphologies in-vitro, and to assess potential medical therapies. However, the intrinsic mechanisms of these systems are not entirely understood yet, which can result in variability of organoids due to differences in culture conditions and basement membrane extracts used. Improving the standardisation of organoid cultures is essential for their implementation in clinical protocols. Developing tools to assess and predict the behaviour of these systems may produce a more robust and standardised biological model to perform accurate clinical studies. Here we developed an algorithm to automate crypt-like structure counting on intestinal organoids in both in-vitro and in-silico images. In addition, we modified an existing two-dimensional agent-based mathematical model of intestinal organoids to better describe the system physiology, and evaluated its ability to replicate budding structures compared to new experimental data we generated. The crypt-counting algorithm proved useful in approximating the average budding structures found in our in-vitro intestinal organoid culture images on days 3 and 7 after seeding. Our changes to the in-silico model maintain the potential to produce simulations that replicate the number of budding structures found on days 5 and 7 of in-vitro data. The present study aims to aid in quantifying key morphological structures and provide a method to compare both in-vitro and in-silico experiments. Our results could be extended later to 3D in-silico models.

systems biology↗

Cross-talk between Hippo and Wnt signalling pathways in intestinal crypts: insightsfrom an agent-based model

Intestinal crypts are responsible for the total cell renewal of the lining of the intestines, occurring every 4-7 days in humans. This rapid turnover is governed by the complex interplay between signalling pathways and the cell cycle within individual cells in the crypts. The role of Wnt signalling in governing cell proliferation and differentiation in the intestinal crypt has been extensively studied, with increased signalling found towards the lower regions of the crypt. Recent studies have shown that the Wnt signalling gradient found within the crypt may arise as a result of division-based spreading from a Wnt reservoir at the crypt base. The discovery of the Hippo pathways involvement in maintaining crypt homeostasis is more recent; a mechanistic understanding of Hippo pathway dynamics, and its possible cross-talk with the Wnt pathway, remains lacking. To explore how the interplay between these pathways may control crypt homeostasis and dysplasia we developed and analysed a mathematical model coupling an ordinary differential equation description of Wnt and Hippo signalling with a cell-based description of cell movement, proliferation and contact inhibition. Furthermore, we compared an imposed Wnt gradient with a division-based Wnt gradient model. Our results suggest that Hippo signalling affects the Wnt pathway by reducing the presence of free cytoplasmic {beta}-catenin, causing cell cycle arrest. This process slows the rate of crypt turnover, previously attributed only to mutations in Wnt pathway components commonly observed in colorectal cancers. We also show that a division-based spreading of Wnt can form a Wnt gradient, resulting in proliferative dynamics comparable to imposed-gradient models. This suggests that imposed-gradient models are a reasonable approximation of experimentally observed Wnt gradients, however they provide little insight into the source of Wnt. Finally, a simulated APC double mutant, with misregulated Wnt and Hippo signalling activity, is predicted to be capable of completing a more rapid monoclonal conversion of the crypt than a Wnt-only mutant.\n\nAuthor summaryColorectal cancer is the fourth leading cause of cancer death worldwide. It is generally established that colorectal cancer occurs upon disruption of the dynamics of crypts, tubular indentations lining the walls of the gastrointestinal tract that are responsible for renewal of the intestinal epithelium. Thus, understanding the mechanisms that regulate intestinal crypt dynamics is instrumental to understand how colorectal cancer can emerge. We used mathematical modelling to explore how crypt dynamics emerge from the interactions across several biological scales, including mutations that cause an abnormal cell response to changes at the cell or tissue level, cell proliferation and motility within the crypt. Our model describes, in each cell within the crypt, levels and dynamics of genes involved in two signalling pathways - the canonical Wnt and Hippo pathways - relevant for cell proliferation and adhesion. In simulations, we predict how the crosstalk between these pathways affects crypt dynamics in both healthy and dysplastic cases. Furthermore, our simulations match recent biological evidence of a novel mechanism, based on cell division, causing heterogeneous and graded localisation of different cell types (dividing or not) within the crypt. Our results suggest the possibility of combined disease treatment, targeting both the Wnt and Hippo pathways.

systems biology↗