bioRxiv ScienceSearch

bioRxiv · 10.1101/660415

Electrophysiological correlates of syntactic structures

Abstract

Syntax is traditionally defined as a specifically human way to pair sound with meaning: words are assembled in a recursive way generating a potentially infinite set of sentences1,2. There can be different phrasal structures depending on the types of words involved, for example, \"noun phrases\" (NP), combining an article and a noun, vs. \"verb phrases\" (VP), combining a verb and a complement. Although it is known that the combination of an increasing number of words in sequences correlates with an increasing electrophysiological activity3,4, the specific electrophysiological correlates of the syntactic operation generating NPs vs. VPs remain unknown. A major confounding factor is the fact that syntactic information is inevitably intertwined with the acoustic information contained in words even during inner speech5. Here, we addressed this issue in a novel way by designing a paradigm to factor out acoustic information and isolate the syntactic component. In particular, we construed phrases that have exactly the same acoustic content but that are interpreted as NPs or VPs depending on their syntactic context (homophonous phrases). By performing stereo-electro-encephalographic (SEEG) recordings in epileptic patients6 we show that VPs are associated with a higher activity in the high gamma band (150-300Hz frequency), an index of cortical activity associated with linguistic processing, with respect to NPs in multiple cortical areas in both hemispheres, including language areas and their homologous in the non-dominant hemisphere. Our findings pave the way to a deeper understanding of the electrophysiological mechanisms underlying syntax and contribute to the ultimate far reaching goal of a complete neural decoding of linguistic structures from the brain2.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Artoni, F., D'Oro, P., Catricala', E., Conca, F., Bottoni, F., Pelliccia, V., Sartori, I., Lo Russo, G., Cappa, S., Micera, S., Moro, A.. 2019-06-06. Electrophysiological correlates of syntactic structures. https://doi.org/10.1101/660415

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

The Unreasonable Effectiveness of Cell Types in Describing Neuronal Physiological Features

Single-cell RNA sequencing (scRNA-seq) captures detailed gene expression profiles at scale, while patch-clamp recordings measure intrinsic neuronal electrophysiological properties. Modeling the relations between these two modalities remains a challenge. Here, we compare how well electrophysiological features can be predicted by traditional transcriptomic cell type classification, representations derived from a foundational model (scGPT) pretrained on large-scale scRNA-seq datasets, ion channel-coding genes, and highly variable genes. Using paired transcriptomic and electrophysiological patch-sequencing data from 495 human neurons from neurosurgical tissue, we find that cluster-level cell type representations consistently outperform highly variable gene selection, ion channel gene selection, and context-enriched scGPT embeddings. Notably, performance varies across model architectures and initializations, and the best results are obtained by combining the outputs of separate cell type and scGPT-based models. Together, these findings suggest that traditional discrete cellular classification is highly effective in predicting physiological features. For maximum performance it can be complemented by pretrained transformer models.

neuroscience

A nonlinear inhibition pathway underlying cortical responses to tuned holographic optogenetic perturbations

Optogenetics enables causal manipulation of cortical activity. Perturbation responses can be counterintuitive due to network interactions, making theory essential for predicting them. Existing approaches often rely on linear approximations, which fail for many biologically relevant perturbations. Here we develop a nonlinear theory of responses to holographic perturbations in cell-type-specific recurrent networks with structured connectivity. We fit a nonlinear model to mouse V1 data, which shows cotuned-ensemble suppression: perturbing spatially clustered neurons with similar preferred orientations yields markedly stronger short-range suppression than perturbing untuned ensembles. We show that cotuned-ensemble suppression arises from a feature-tuned, nonlinear inhibition pathway implicating somatostatin-positive (SST) interneurons. The theory predicts that cotuned ensembles suppress parvalbumin-positive (PV) neurons but facilitate SST neurons, and links the degree of cotuned-ensemble suppression or facilitation to the variance of the SST response. This framework identifies mechanisms by which nonlinear inhibition sculpts cortical dynamics and establishes a predictive basis for targeted optogenetic interventions.

neuroscience

Proteomic signatures of APOE ε4 across human tissues and cell types in Alzheimers disease

The apolipoprotein E {varepsilon}4 (APOE {varepsilon}4) allele is the strongest genetic risk factor for late-onset Alzheimers disease (AD). However, the underlying molecular mechanisms remain unclear. This study included 1691 participants from the Religious Orders Study and Rush Memory and Aging Project (ROSMAP), 1226 participants from the Accelerating Medicines Partnership - Alzheimers Disease (AMP-AD) Diverse Cohorts Study, and 735 participants from the Alzheimers Disease Neuroimaging Initiative (ADNI). To characterise APOE {varepsilon}4 molecular effects, we analysed proteomic data from plasma, cerebrospinal fluid (CSF), and induced pluripotent stem cell (iPSC)-derived astrocytes and neurons, as well as transcriptomic and proteomic data from multiple brain regions. The association of APOE {varepsilon}4 with AD neuropathology was also examined. APOE {varepsilon}4 carriers shared a plasma proteomic signature enriched for immune processes, irrespective of AD diagnosis. A machine learning classifier trained on this signature discriminated APOE {varepsilon}4 carriers from non-carriers in an independent cohort using CSF proteomics. APOE {varepsilon}4 carriage was associated with higher Braak stages and Consortium to Establish a Registry for Alzheimers Disease (CERAD) score. However, only limited APOE {varepsilon}4-associated transcriptomic and proteomic changes were observed in bulk brain tissue, with poor cross-layer concordance. Proteomic analyses of iPSC-derived astrocytes and neurons further revealed cell-type-specific APOE {varepsilon}4-associated changes. APOE {varepsilon}4 is associated with a consistent proteomic signature across plasma and CSF. Its molecular effects in the brain differ across cell types, brain regions and molecular layers. These findings support the need for cell-type-resolved multi-omic studies to elucidate how APOE {varepsilon}4 confers AD risk.

neuroscience