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Clarke, A.

Publications and source records attributed to Clarke, A..

At least 19 recordsLinked to original sources

Prior visual context accelerates the emergence of object representations

Our knowledge about how the world is structured allows for predictions about what objects we might see next. Visual context is known to impact the perception of subsequent objects, but we do not know what context does to the mental representation of those objects. Using MEG, we tested how a scene context changes the neural representation of visual objects, and whether the context simply enhances expected object representations, or if it acts to reorganise the temporal trajectory of object information in the brain. Using temporal generalisation decoding, we show that multiple dimensions of semantic information are shifted up to 200 ms earlier when the object and the prior context are congruent, and this temporally-shifted decoding was related to behavioural object recognition speed. This suggests that prior context can warp the temporal trajectory through which object representations are accessed and accelerate the emergence of semantic object representations in the mind.

neuroscience↗

The avocado pangenome reveals dynamic clustering and lineage-specific diversity of NLR genes

Avocado is an economically important perennial tree crop with a complex domestication history, yet modern genomic resources are limited. We present the first high-quality avocado pangenome, spanning seven diverse accessions across Mexican, Guatemalan, and West-Indian lineages. PacBio HiFi, partially phased assemblies deliver near chromosome-level continuity (N50 ~57 Mb; BUSCO >96%), and functional annotations show enrichment of immune-related families. Core-accessory partitioning indicates adaptive functions -- pathogen response and secondary metabolism -- are overrepresented in accessory genes. Nucleotide-binding Leucine-rich repeat (NLR) genes were catalogued (226-256 per accession), showing lineage-specific expansions, diverse domain architectures, and frequent chromosomal clustering. Structural variants concentrate within NLR loci, marking hotspots of pathogen-detection diversification. Comparative analyses show ~54% of NLRs are shared, with extensive functional and sequence diversity among accessions. Together, these results define the avocado NLRome and its core- accessory interplay, providing a graph-based framework to accelerate discovery of resistance loci and breeding for durable disease resistance.

plant biology↗

TASL is required for age-related B cell formation and autoimmunity

The autoimmune disease systemic lupus erythematosus (SLE) is associated with genetic variants in the X-linked gene CXORF21, which encodes the protein TASL. TASL acts as an adaptor in the IRF5 pathway and is necessary for the phosphorylation of IRF5 in response to TLR7 or TLR9 stimulation. Here, we investigate the role of TASL in the humoral immune response, and in the development of lupus in the B6.MRLlpr murine model of SLE. We find that while TASL is dispensable for their development, it is required for the full activation of B cells via endolysosomal TLR stimulation, and consequent interferon signalling and inflammatory cytokine expression. Additionally, TASL is crucial for the emergence of age-associated B cells (ABCs), a B cell population derived from the extrafollicular response that increases with age and is expanded in autoimmune disease, and the production of IgG2c antibodies. We also find that deletion of TASL prevents the onset of autoimmunity in the genetically-determined B6.MRLlpr model of lupus.

immunology↗

All spectral frequencies of neural activity reveal semantic representation in the human anterior ventral temporal cortex

Intracranial electrophysiology offers a unique insight into the nature of information representation in the brain - it can be used to disentangle information encoded in local neuronal activity (gamma and high gamma frequencies) from information encoded via long-range interactions (lower frequencies). We used regularised logistic regression to decode animacy from time-frequency power and phase extracted from electrocorticography (ECoG) grid electrode data recorded on the surface of human vATL. Power in gamma (30 - 60 Hz) and high gamma (60 - 200 Hz) produced reliable decoding, indicating that semantic information is indeed expressed by local populations in vATL. However, power from a wide range of frequencies (4 - 200 Hz) produced significantly higher decoding accuracy and also exhibited the same rapidly-changing dynamic code previously observed when decoding voltage. These findings support the theory that semantic information is encoded by a local vATL "hub" that interacts with distributed cortical "spokes".

neuroscience↗

Neural oscillations and top-down connectivity are modulated by object-scene congruency

The knowledge we have about how the world is structured is known to influence object recognition. One way this is demonstrated is through a congruency effect, where object recognition is faster and more accurate if items are presented in expected scene contexts. However, our understanding of the dynamic neural mechanisms that underlie congruency effects are under-explored. Using MEG, we examine how the congruency between an object and a prior scene results in changes in the oscillatory activity in the brain, which regions underpin this effect, and whether congruency results arise from top-down or bottom-up modulations of connectivity. We observed that prior scene information impacts the processing of visual objects in behaviour, neural activity and connectivity. Processing objects that were incongruent with the prior scene resulted in slower reaction times, increased low frequency activity in the ventral visual pathway, and increased top-down connectivity from the anterior temporal lobe and frontal cortex to the posterior ventral temporal cortex. Our results reveal that the recurrent dynamics within the ventral visual pathway are modulated by the prior knowledge imbued by our surrounding environment, suggesting that the way we recognise objects is fundamentally linked to their context.

neuroscience↗

Glycogen synthase kinase-3 is essential for Treg development and function

Tregs are critical regulators of the immune response, but the cellular signalling pathways that control their development and homeostasis remain to be determined. We found that glycogen synthase kinase-3 (GSK3), a kinase which integrates signals from AKT and mTOR, was essential for Treg development, restraining fatal autoimmunity. Loss of Gsk3 led to metabolic rewiring in Tregs, with disordered nucleotide metabolism and activation of OxPhos. Acute deletion of Gsk3 did not affect Treg frequency or numbers, but induced an effector gene expression program, and led to the formation of populations with pro-inflammatory signatures. The loss of Gsk3 in Tregs profoundly enhanced anti-tumoral immune responses and suppressed tumour growth.

immunology↗

Capturing changes to animal complexity from quantifiable patterns in genomic data

A prevailing problem in evolutionary biology is elucidating the "genotype-phenotype map" that characterizes how genomic activities regulate different aspects of organismal morphology and their variability in both space and time. Here, we explore potential causality between genome content and both morphological complexity and disparity by compiling the regulatory components (i.e., transcription factors, RNA binding proteins, and microRNA families) as well as a representative set of non-regulatory "housekeeping genes" in 32 species belonging to a wide variety of animal phyla, altogether encapsulating a number of varying genomic characteristics and morphological diversities. A principal component analysis of these four non-overlapping genomic components from each of these 32 species in relation to their last common ancestor revealed that no relationship exists between genome space and disparity, as changes to animal body plans appear to be largely the result of changes to the gene regulatory networks that govern animal development rather than gaining or losing specific sets of regulatory genes. However, using both phylogenetically correlated as well as phylogenetically uncorrelated statistical tests, we find a strong relationship between the loss of all considered gene types and the advent of some parasitic taxa, as well as between microRNA innovations and organismal complexity. While this analysis of genomic features suggests how complexity and disparity are each encoded in the genome, further analysis of the regulatory networks in which they participate should provide a more comprehensive description of how organisms diversify their morphologies over time through alterations in their genomic components. SIGNIFICANCE STATEMENTVariation in morphological form can be measured by considering either disparity (i.e., the amount of variance in morphological form) or complexity (i.e., the difference in the number of their "parts" including genes or cells). To date, discerning the genomic basis of either has remained largely unknown. Here, we compile the regulatory genome of the last common ancestor of bilaterian metazoans, including its transcription factors, RNA-binding proteins and microRNA families, and ask how changes to these repertoires potentially reflects changes in either disparity or complexity. We find that although there is no relationship between the regulatory genome and disparity, there is a robust relationship between the loss of regulatory genes relative to housekeeping genes, especially in parasitic taxa. Further, there is a strong relationship between increases to microRNAs and complexity, which likely reflects the unique role microRNAs play in increasing both the accuracy and the precision of gene expression during development.

evolutionary biology↗

Congruency effects on object recognition persist when objects are placed in the wild: An AR and mobile EEG study

Objects in expected locations are recognised faster and more accurately than objects in incongruent environments. This congruency effect has a neural component, with increased activity for objects in incongruent environments. Studies have increasingly shown differences between neural processes in realistic environments and tasks, and neural processes in the laboratory. Here, we aimed to push the boundaries of traditional cognitive neuroscience by tracking the congruency effect for objects in real world environments, outside of the lab. We investigated how neural activity is modulated when objects are placed in real environments using augmented reality while recording mobile EEG. Participants approached, viewed, and rated how congruent they found the objects with the environment. We found significant differences in ERPs and higher theta-band power for objects in incongruent contexts than objects in congruent contexts. This demonstrates that real-world contexts impacts how objects are processed, and that mobile brain imaging and augmented reality are effective tools to study cognition in the wild.

neuroscience↗

Intact reinforcement learning in healthy ageing

What does age in ageing? Results in reinforcement learning (RL) are mixed. Some studies found deteriorated performance in older participants compared to younger controls whereas other studies did not. Daniel et al. (2020) suggested that task demand can explain these differences, with less demanding tasks showing no effect of age. Here, we increased the task demand of previous studies turning them into a classic navigation task. We extracted 4 behavioral parameters and 2 parameters (learning and exploration rates) of a classic Q-learning model. Except for one specific parameter, all other parameters showed no group differences, i.e., RL turned out to be intact in older individuals also with higher task demands. It is important to publish such null results to avoid the stigmatizing impression of an overall performance deficit among older people.

neuroscience↗

Asparagine availability controls germinal centre B cell homeostasis

Germinal centre (GC) B cells proliferate at some of the highest rates of any mammalian cell, yet the metabolic processes which enable this are poorly understood. We performed integrated metabolomic and transcriptomic profiling of GC B cells, and found that metabolism of the non-essential amino acid asparagine (Asn) was highly upregulated. Asn was conditionally essential to B cells, and its synthetic enzyme, asparagine synthetase (ASNS) was upregulated following their activation, particularly more markedly in the absence of Asn, through the integrated stress response sensor general control non-derepressible 2 (GCN2). When Asns is deleted B cell survival and proliferation in low Asn conditions were strongly impaired, and removal of environmental Asn by asparaginase or dietary restriction markedly compromised the GC reaction, impairing affinity maturation and the humoral response to influenza infection. Using stable isotope tracing and single cell RNA sequencing, we found that metabolic adaptation to the absence of Asn requires ASNS, and that oxidative phosphorylation, mitochondrial homeostasis, and synthesis of nucleotides was particularly sensitive to Asn deprivation. Altogether, we reveal that Asn metabolism acts as a key regulator of B cell function and GC homeostasis. The one sentence summaryAsparagine metabolism is a critical regulator of B cell function, maintaining the germinal centre reaction.

immunology↗

Changes in local interaction rules during ontogeny underlie the evolution of collective behavior

Collective motion emerges from individual interactions which produce groupwide patterns in behavior. While adaptive changes to collective motion are observed across animal species, how local interactions change when these collective behaviors evolve is poorly understood. Here, we use the Mexican tetra, A. mexicanus, which exists as a schooling surface form and a non-schooling cave form, to study differences in how fish alter their swimming in response to neighbors across ontogeny and between evolutionarily diverged populations. We find that surface fish undergo a transition to schooling during development that occurs through increases in inter-individual alignment and attraction mediated by changes in the way fish modulate speed and turning relative to neighbors. Cavefish, which have evolved loss of schooling, exhibit neither of these schooling-promoting interactions at any stage of development. These results reveal how evolution alters local interaction rules to produce striking differences in collective behavior.

evolutionary biology↗

Hearing what is being said: The distributed neural substrate for early speech interpretation

Speech comprehension is remarkable for the immediacy with which the listener hears what is being said. Here, we focus on the neural underpinnings of this process in isolated spoken words. We analysed source-localised MEG data for nouns using Representational Similarity Analysis to probe the spatiotemporal coordinates of phonology, lexical form, and the semantics of emerging word candidates. Phonological model fit was detectable within 40-50 ms, engaging a bilateral network including superior and middle temporal cortex and extending into anterior temporal and inferior parietal regions. Lexical form emerged within 60-70 ms, and model fit to semantics from 100-110 ms. Strikingly, the majority of vertices in a central core showed model fit to all three dimensions, consistent with a distributed neural substrate for early speech analysis. The early interpretation of speech seems to be conducted in a unified integrative representational space, in conflict with conventional views of a linguistically stratified representational hierarchy.

neuroscience↗

Recurrent connectivity supports higher-level visual and semantic object representations in the brain

Visual object recognition is a dynamic process by which we rapidly extract meaningful information about the things we see. However, the functional relevance of inter-regional feedforward and feedback signals in the human ventral visual pathway remain largely unspecified, while its unclear whether computational models of vision alone can accurately capture object-specific representations. Here, we probe these dynamics using a combination of representational similarity and connectivity analyses of fMRI and MEG data recorded during the recognition of familiar, unambiguous objects. Modelling the visual and semantic properties of our stimuli using an artificial neural network as well as a semantic feature model, we find that unique aspects of the neural architecture and connectivity dynamics relate to visual and semantic object properties. Critically, we show that recurrent processing between anterior and posterior ventral temporal cortex relates to higher-level visual properties prior to semantic object properties, in addition to semantic-related feedback from the frontal lobe to the ventral temporal lobe between 250 and 500ms after stimulus onset. These results demonstrate the distinct contributions made by semantic object properties in explaining neural activity and connectivity, highlighting it as a core part of object recognition not fully accounted for by biologically inspired neural networks.

neuroscience↗

LAT1 enables T cell activation under inflammatory conditions: a new therapeutic target for rheumatoid arthritis

ObjectiveTo assess the L-type amino acid transporter-1 (LAT1) as a possible therapeutic target for rheumatoid arthritis (RA). MethodsSynovial LAT1 expression was monitored by immunohistochemistry and transcriptomic datasets. The contribution of LAT1 to gene expression and immune synapse formation was assessed by RNA-sequencing and total internal reflection fluorescent (TIRF) microscopy, respectively. Mouse models of RA were used to assess the impact of therapeutic targeting of LAT1. ResultsLAT1 was strongly expressed by CD4+ T cells in the synovial membrane of patients with active RA and the level of expression correlated with levels of ESR and CRP as well as DAS-28 scores. Deletion of LAT1 in murine CD4+ T cells inhibited the development of experimental arthritis and prevented the differentiation of CD4+ T cells expressing IFN-{gamma} and TNF-, without affecting regulatory T cells. LAT1 deficient CD4+ T cells demonstrated reduced transcription of genes associated with TCR/CD28 signalling, including Akt1, Akt2, Nfatc2, Nfkb1 and Nfkb2. Functional studies using TIRF microscopy revealed a significant impairment of immune synapse formation with reduced recruitment of CD3{zeta} and phospho-tyrosine signalling molecules in LAT1 deficient CD4+ T cells from the inflamed joints but not the draining lymph nodes of arthritic mice. Finally, it was shown that a small molecule LAT1 inhibitor, currently undergoing clinical trials in man, was highly effective in treating experimental arthritis in mice. ConclusionsIt was concluded that LAT1 plays a critical role in activation of pathogenic T cell subsets under inflammatory conditions and represents a promising new therapeutic target for RA. Key MessagesO_ST_ABSWhat is already known about this subject?C_ST_ABSO_LILAT1 is an amino acid transporter that has previously been shown to play a role in T cell activation. C_LI What does this study add?O_LILAT1 is expressed by synovial T cells in human rheumatoid arthritis and the level of expression correlates with disease severity. C_LIO_LILAT1 expression by T cells is necessary for development of severe arthritis in animal models. C_LIO_LILAT1 is required for immune synapse formation and activation of pathogenic CD4+ T cell subsets in the inflamed joint, but not the lymph nodes. C_LIO_LIA small molecular weight LAT1 inhibitor, currently in clinical trials for cancer, is highly effective in animal models of rheumatoid arthritis. C_LI How might this impact on clinical practice of future developments?O_LIThe context-specific nature of LAT1 involvement in T cell activation positions it as an ideal therapeutic target to distinguish between pathogenic and protective T cell responses and this study provides the scientific rationale for clinical evaluation of LAT1 inhibitors in the treatment of rheumatoid arthritis. C_LI

immunology↗

Semantic object processing is modulated by prior scene context

Objects that are congruent with a scene are recognised more efficiently than objects that are incongruent. Further, semantic integration of incongruent objects elicits a stronger N300/N400 EEG component. Yet, the time course and mechanisms of how contextual information supports access to semantic object information is unclear. We used computational modelling and EEG to test how context influences semantic object processing. Using representational similarity analysis, we established that EEG patterns dissociated between objects in congruent or incongruent scenes from around 300 ms. By modelling semantic processing of objects using independently normed properties, we confirm that the onset of semantic processing of both congruent and incongruent objects is similar ([~]150 ms). Critically, after [~]275 ms, we discover a difference in the duration of semantic integration, lasting longer for incongruent compared to congruent objects. These results constrain our understanding of how contextual information supports access to semantic object information.

neuroscience↗

Dynamic mitochondrial transcription and translation in B cells control germinal centre entry and lymphomagenesis

Germinal centre (GC) B cells undergo proliferation at very high rates in a hypoxic microenvironment, but the cellular processes driving this are incompletely understood. Here we show that the mitochondria of GC B cells are highly dynamic, with significantly upregulated transcription and translation rates associated with the activity of transcription factor mitochondrial A (TFAM). TFAM, whilst also necessary for normal B cell development, is required for entry of activated GC-precursor B cells into the germinal centre reaction, and deletion of Tfam significantly impairs GC formation, function, and output. Loss of TFAM in B cells compromises the actin cytoskeleton and impairs cellular motility of GC B cells in response to chemokine signalling, leading to their spatial disorganisation. We show that B cell lymphoma substantially increases mitochondrial translation, and deletion of Tfam in B cells is protective against the development of lymphoma in a c-Myc transgenic model. Finally, we show that pharmacologic inhibition of mitochondrial transcription and translation inhibits growth of GC-derived human lymphoma cells, and induces similar defects in the actin cytoskeleton.

immunology↗

Enabled primarily controls filopodial morphology, not actin organization, in the TSM1 growth cone in Drosophila

Ena/VASP proteins are processive actin polymerases that are required throughout animal phylogeny for many morphogenetic processes, including axon growth and guidance. Here we use live imaging of morphology and actin organization in the TSM1 axon of the Drosophila wing to dissect the mechanism of Ena action. We find that altering Ena activity has a substantial impact on filopodial morphology in this growth cone, but exerts only modest effects on actin organization. This is in contrast to the main regulator of Ena, Abl tyrosine kinase, which has profound effects on actin and only mild effects on TSM1 growth cone morphology. These data suggest that the primary role of Ena in this axon may be to link actin to morphogenetic processes of the plasma membrane, rather than regulating actin organization itself. These data also suggest that a key role of Ena, acting downstream of Abl, may be to maintain a constant filopodial organization of the growth cone, even as Abl activity varies in response to guidance cues in the environment. Summary statementWe dissect the function of the actin polymerase, Enabled, in axon growth by live-imaging of actin dynamics and axon morphology of the TSM1 neuron in its native environment in vivo.

neuroscience↗

Plasma iron controls neutrophil production and function

Low plasma iron (hypoferremia) induced by hepcidin is a conserved inflammatory response that protects against infections but inhibits erythropoiesis. How hypoferremia influences leukocytogenesis is unclear. Using proteomic data, we predicted that neutrophil production would be profoundly more iron-demanding than generation of other white blood cell types. Accordingly in mice, hepcidin-mediated hypoferremia substantially reduced numbers of granulocytes but not monocytes, lymphocytes or dendritic cells. Neutrophil rebound after anti-GR1-induced neutropenia was blunted during hypoferremia, but was rescued by supplemental iron. Similarly, hypoferremia markedly inhibited pharmacologically-stimulated granulopoiesis mediated by GCSF and inflammation-induced accumulation of neutrophils in the spleen and peritoneal cavity. Furthermore, hypoferremia specifically altered neutrophil effector functions, suppressing antibacterial mechanisms but enhancing mitochondrial ROS-dependent NETosis associated with chronic inflammation. Notably, antagonising endogenous hepcidin during acute inflammation enhanced production of neutrophils. We propose plasma iron modulates the profile of innate immunity by controlling monocyte-to-neutrophil ratio and neutrophil activity in a therapeutically targetable system.

immunology↗