bioRxiv Science⌕ Search

Biology subjects

Marino, S.

Publications and source records attributed to Marino, S..

13 recordsLinked to original sources

Perceived Control Over Breathing Perturbations Depends on Interosensory Input and Prediction Error

Interoception and homeostatic/allostatic control are not only fundamental for survival but play a key role for maintaining somatic and mental health. Furthermore, metacognitive evaluations of these processes, such as perceived failure of allostatic regulation, have been proposed to underlie the experience of chronic symptoms, such as chronic fatigue. A central question in this regard is what mechanisms the brain uses to evaluate control over bodily states. A prominent computational proposal posits that this is achieved by monitoring of interoceptive prediction errors (PEs). However, to date, this proposal has not been tested experimentally. Here, we tested this hypothesis by applying computational process models of perceived control to data from a novel behavioural paradigm, the Respiratory Metacognition of Control Task (RMCT). The RMCT manipulates control over breathing by changing inspiratory resistive loads as a function of control achieved in a gamified prediction task. We developed and compared trial-by-trial generative models of perceived explicit control in the RMCT, using data from 50 volunteers in a pre-registered analysis. Bayesian model selection suggested that perceived control over breathing is best explained as a function of both trial-wise interoceptive outcomes (breathing with or without an inspiratory resistive load) and trial-wise PEs about respiratory resistance. These results support a longstanding computational proposal of how the brain detects failures of bodily regulation and provide a mechanistic model for understanding inter-individual differences in perceived control over bodily states.

neuroscience↗

Mouse Bio-behavioral Phenotyping Using a Digital Homecage Framework for Long-timescale, High-resolution, and Multi-factor Data Collection and Analytics

MOTIVATION Long-term monitoring of behavioral and physiological processes is critical for understanding complex brain-based phenomena and disorders that develop over extended periods, such as chronic stress, circadian disorders, and metabolic conditions. While digital phenotyping is available in humans using smart devices, there remains a deficit in rodent models. To address this lack of long-term rodent phenotyping, we introduce the "Digital Homecage" (DHC) system. Our system uses accessible components and is designed for seamless integration with brain recording technologies. The Digital Homecage (DHC) allows uninterrupted, long-timescale recording of more than 20 behavioral metrics in single-housed mice, captured at sub-second resolution via video, operant interactions, and wheel-running data. This report demonstrates the DHCs capacity to enable continuous, automated tracking of behaviors like actigraphy, sleep, grooming, and food choice options over weeks, thereby opening up new avenues for longitudinal analyses of chronic conditions. Data collected reveal circadian patterns in multiple spontaneous behaviors, aligning with known nocturnal tendencies. The systems potential to facilitate groundbreaking observations on the long-term behavioral correlates of various neuropsychiatric syndromes is aided by open-source software and relatively low cost. The DHC sets the stage for community-driven innovation, potentially transforming our approach to studying complex traits of brain function and behavior in laboratory settings.

animal behavior and cognition↗

Test-retest reliability of auditory MMN measured with OPM-MEG

In this paper, we report results from an investigation of auditory mismatch responses as measured by magnetoencephalography (MEG) based on optically pumped magnetometers (OPM). Specifically, as part of a quality control study, we examined the reliability and validity of auditory mismatch negativity (MMN) recordings, obtained with a newly installed OPM-MEG system. Based on OPM-MEG data from 30 healthy volunteers, measured twice with an established auditory MMN paradigm with frequency deviants, we examined the following questions: First, we focused on construct validity and examined whether OPM-MEG measurements of MMN responses (in terms of event-related fields, ERFs) were qualitatively comparable to previous MMN findings from studies using EEG or MEG based on superconducting quantum interference devices (SQUIDs). In particular, we examined whether significant MMN responses measured by OPM-MEG occurred in a comparable time window and showed a similar topography as in previous EEG/MEG studies of MMN. Second, we quantified test-retest reliability of MMN amplitude and latency over two separate measurement sessions. The results of our analyses show that MMN responses recorded with OPM-MEG are in good agreement with previously reported MMN results in terms of timing and topography. Furthermore, the comparison of group-level MMN topographies and timeseries shows excellent consistency across the two measurement sessions. Our quantitative test-retest reliability analyses at the sensor level indicate good reliability for MMN amplitude, but poor reliability for MMN latency. Overall, our findings suggest that OPM-MEG measurements of auditory MMN (i) are comparable to results from EEG and SQUID-based MEG and (ii) show good test-retest reliability for amplitude measures at the sensor level. Notably, these results were achieved in an "out of the box" state of the OPM-MEG system, shortly after installation and without further optimisation. The reason for the insufficient reliability for MMN latency we observed is currently under investigation and represents an important target for future improvements.

neuroscience↗

Modelling medulloblastoma pathogenesis and treatment in human cerebellar organoids.

Faithful genetically engineered in vivo models of medulloblastoma (MB) are currently available only for some molecular subgroups, in keeping with recent studies showing the unique role of human-specific progenitors in the development of G3 and G4 MB subgroups. We generated human cerebellar organoids (CbO) from expanded potential stem cells (EPSC) and characterised their epigenetic and transcriptomic profile compared to the developing human cerebellum. We show the presence of sub compartment-specific cerebellar lineages linked to MB formation, including populations expressing signature genes of putative G3 and G4 MB cells-of-origin. We show that these lineages can be genetically engineered to model MB tumour onset. Moreover, we demonstrate that CbO sustain proliferation and invasion of G3/4 MB cells in a 3D co-culture model (CbO-MB) while preserving their molecular identity, and that treatment of CbO-MB with anti-tumour compounds recapitulate the efficacy of in vivo drug testing in xenograft models.

cancer biology↗

The invasion phenotypes of glioblastoma depend on plastic and reprogrammable cell states

Glioblastoma (GBM), the most common primary brain cancer in adults, is characterized by rapid local invasion along diverse routes, such as infiltration of white matter tracts and penetration of perivascular spaces. We investigate the hypothesis that GBM invasion routes correlate with the transcriptional states of individual cells and identify regulators of route-specific invasion. Utilizing patient-derived GBM xenograft models, we integrate single-cell transcriptomics and spatial proteomics, revealing that mesenchymal and oligodendrocyte progenitor-like GBM cells migrate perivascularly, while neural progenitor and astrocyte-like GBM cells invade diffusely. Computational reconstruction identifies ANXA1 as a perivascular invasion driver and lineage-restricted transcription factors RFX4 and HOPX as drivers of diffuse invasion, predictive of patient survival. Genetic ablation of these genes alters invasion phenotypes and extends survival in xenografted mice, clarifying the role of cell states in GBM invasion, and highlighting potential therapeutic targets for selective invasion route targeting in GBM patients.

cancer biology↗

The inflammatory micro-environment induced by targeted CNS radiotherapy is underpinned by disruption of DNA methylation

Although targeted radiotherapy (RT) is integral to the increasing survival of cancer patients, it has significant side-effects, the cellular and molecular mechanisms of which are not fully understood. During RT epigenetic changes occur in neoplastic tissue, but few studies have assessed these in non-neoplastic tissue and results are highly variable. Using bulk DNA methylation and RNA sequencing as well as spatial transcriptomics (ST) in a unique cohort of patient tissue samples, we show distinct differences in DNA methylation patterns in irradiated brain tissue, whilst ST characterisation identifies specific micro-environmental niches present after irradiation and highlights neuropeptides that could be propagating neuroinflammation. We also show that in a cerebral organoid (CO) model of early changes in neurons after irradiation there are similar DNA methylation alterations and disruption of the DNA methylation machinery, suggesting that early but persistent epigenetic dysregulation plays a role in neurotoxicity. We provide a link between radiotherapy induced neuroinflammation and disruption of DNA methylation for the first time and suggest possible driving mechanisms for this chronic neuroinflammation.

neuroscience↗

Mapping chromatin remodelling in glioblastoma identifies epigenetic regulation of key molecular pathways and novel druggable targets.

Analysis of chromatin remodelling in neoplastic stem cells as compared to ontogenetically related neural stem cells, reveals multifactorial epigenetic regulation of signalling pathways known to contribute to glioblastoma development. It also identifies novel epigenetically regulated druggable target genes on a patient-specific level, including SMOX and GABBR2 which could be further developed for future translational approaches to more effectively treat this neoplasm.

cancer biology↗

Bayesian Workflow for Generative Modeling in Computational Psychiatry

Computational (generative) modelling of behaviour has considerable potential for clinical applications. In order to unlock the potential of generative models, reliable statistical inference is crucial. For this, Bayesian workflow has been suggested which, however, has rarely been applied in Translational Neuromodeling and Computational Psychiatry (TN/CP) so far. Here, we present a worked example of Bayesian workflow in the context of a typical application scenario for TN/CP. This application example uses Hierarchical Gaussian Filter (HGF) models, a family of computational models for hierarchical Bayesian belief updating. When equipped with a suitable response model, HGF models can be fit to behavioural data from cognitive tasks; these data frequently consist of binary responses and are typically univariate. This poses challenges for statistical inference due to the limited information contained in such data. We present a novel set of response models that allow for simultaneous inference from multivariate (here: two) behavioural data types. Using both simulations and empirical data from a speed-incentivised associative reward learning (SPIRL) task, we show that harnessing information from two different data streams (binary responses and continuous response times) improves the accuracy of inference (specifically, identifiability of parameters and models). Moreover, we find a linear relationship between log-transformed response times in the SPIRL task and participants uncertainty about the outcome. Our analysis illustrates the benefits of Bayesian workflow for a typical use case in TN/CP. We argue that adopting Bayesian workflow for generative modelling helps increase the transparency and robustness of results, which in turn is of fundamental importance for the long-term success of TN/CP.

neuroscience↗

Global hypo-methylation in a subgroup of glioblastoma enriched for an astrocytic signature is associated with increased invasion and altered immune landscape

We describe a new molecular subgroup of glioblastoma, the most prevalent malignant adult brain tumour, harbouring a bias towards hypomethylation at defined differentially methylated regions. This epigenetic signature correlates with an enrichment for an astrocytic gene signature, which together with the identification of enriched predicted binding sites of transcription factors known to cause demethylation and to be involved in astrocytic/glial lineage specification, point to a shared ontogeny between this glioblastoma subgroup and astroglial progenitors. At functional level, increased invasiveness, at least in part mediated by SRPX2, and macrophage infiltration characterise this glioblastoma subgroup.

cancer biology↗

Interoception of breathing and its relationship with anxiety

Interoception, the perception of internal bodily states, is thought to be inextricably linked to affective qualities such as anxiety. While interoception spans sensory to metacognitive processing, it is not clear whether anxiety is differentially related to these processing levels. Here we investigated this question in the domain of breathing, using computational modelling and high-field (7 Tesla) fMRI to assess brain activity relating to dynamic changes in inspiratory resistance of varying predictability. Notably, the anterior insula was associated with both breathing-related prediction certainty and prediction errors, suggesting an important role in representing and updating models of the body. Individuals with low vs. moderate anxiety traits showed differential anterior insula activity for prediction certainty. Multimodal analyses of data from fMRI, computational assessments of breathing-related metacognition, and questionnaires demonstrated that anxiety-interoception links span all levels from perceptual sensitivity to metacognition, with strong effects seen at higher levels of interoceptive processes.

neuroscience↗

The Filter Detection Task for measurement of breathing-related interoception and metacognition

The study of the brains processing of sensory inputs from within the body ( interoception) has been gaining rapid popularity in neuroscience, where interoceptive disturbances are thought to exist across a wide range of chronic physiological and psychological conditions. Here we present a task and analysis procedure to quantify specific dimensions of breathing-related interoception, including interoceptive sensitivity (accuracy), decision bias, metacognitive bias, and metacognitive performance. Two major developments address some of the challenges presented by low trial numbers in interoceptive experiments: (i) a novel adaptive algorithm to maintain task performance at 70-75% accuracy; (ii) an extended hierarchical metacognitive model to estimate regression parameters linking metacognitive performance to relevant (e.g. clinical) variables. We demonstrate the utility of the task and analysis developments, using both simulated data and three empirical datasets. This methodology represents an important step towards accurately quantifying interoceptive dimensions from a simple experimental procedure that is compatible with clinical settings.

neuroscience↗

Compressive Big Data Analytics: An Ensemble Meta-Algorithm for High-dimensional Multisource Datasets

Health advances are contingent on continuous development of new methods and approaches to foster data driven discovery in the biomedical and clinical health sciences. Open-science offers hope for tackling some of the challenges associated with Big Data and team-based scientific discovery. Domain-independent reproducibility, area-specific replicability, curation, analysis, organization, management and sharing of health-related digital objects are critical components. This study expands the functionality and utility of an ensemble semi-supervised machine learning technique called Compressive Big Data Analytics (CBDA). Applied to high-dimensional data, CBDA identifies salient features and key biomarkers for reliable and reproducible forecasting of binary or multinomial outcomes. The method relies on iterative subsampling, combines function optimization and statistical inference, and generates ensemble predictions of observed univariate outcomes. In this manuscript, we extend the CBDA technique by (1) efficiently handling extremely large datasets, (2) generalizing the internal and external validation steps, (3) expanding the set of base-learners for joint ensemble prediction, (4) introduce an automated selection of CBDA specifications, and (5) provide mechanisms to assess CBDA convergence, evaluate the prediction accuracy, and measure result consistency. We validated the CBDA 2.0 technique using synthetic datasets as well as a population-wide census-like study, which grounds the mathematical models and the computational algorithm into translational health research settings. Specifically, we empirically validated the CBDA technique on a large-scale clinical study (UK Biobank), which includes imaging, cognitive, and clinical assessment data. The UK Biobank archive presents several difficult challenges related to the aggregation, harmonization, modeling, and interrogation of the information. These problems are related to the complex longitudinal structure, feature heterogeneity, multicollinearity, incongruency, and missingness, as well as violations of classical parametric assumptions that require novel health analytical approaches. Our results showcase the scalability, efficiency and potential of CBDA to compress complex data into structural information leading to derived knowledge and translational action. The results of the real case-study suggest new and exciting avenues of research in the context of identifying, tracking, and treating mental health and aging-related disorders. Following open-science principles, we share the entire end-to-end protocol, source-code, and results. This facilitates independent validation, result reproducibility, and team-based collaborative discovery.

bioinformatics↗

Correlated seed failure as an environmental veto to synchronize reproduction of masting plants

Highly variable, synchronized seed production, called masting, is a widespread reproductive strategy in plants. Resource dynamics, pollination success, and, as described here, environmental veto, are possible proximate mechanisms of masting. We extended the resource budget model of masting with correlated and uncorrelated reproductive failure, and ran this model across its parameters space. Next, we parametrized the model based on a 16-year seed production data for red (Quercus rubra) and white (Q. alba) oaks. Simulations showed that resource dynamics and reproduction failure produce masting even in the absence of pollen coupling. In concordance, in both species, among-year variation in resource gain and correlated reproductive failure were necessary and sufficient to produce masting. Environmental variation is a form of reproduction failure caused by environmental veto that may drive large-scale synchronization without density-dependent pollen limitation. Reproductive-inhibiting weather events are prevalent in ecosystems, suggesting that these described mechanisms likely operate in many masting systems.

ecology↗