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The ability of cortical networks to integrate information from different sources is essential for cognitive processes. On one hand, sensory areas exhibit fast dynamics often phase-locked to stimulation; on the other hand, frontal lobe areas with slow response latencies to stimuli must integrate and maintain information for longer periods. Thus, cortical areas may require different timescales depending on their functional role. Studying the cortical somatosensory network while monkeys discriminated between two vibrotactile stimulus patterns, we found that a hierarchical order could be established across cortical areas based on their intrinsic timescales. Further, even though subareas (areas 3b, 1, and 2) of the primary somatosensory (S1) cortex exhibit analogous firing rate responses, a clear differentiation was observed in their timescales. Importantly, we observed that this inherent timescale hierarchy was invariant between task contexts (demanding vs. nondemanding). Even if task context severely affected neural coding in cortical areas downstream to S1, their timescales remained unaffected. Moreover, we found that these time constants were invariant across neurons with different latencies or coding. Although neurons had completely different dynamics, they all exhibited comparable timescales within each cortical area. Our results suggest that this measure is demonstrative of an inherent characteristic of each cortical area, is not a dynamical feature of individual neurons, and does not depend on task demands.

Even though humans are mostly not aware of their heartbeats, several heartbeat-related effects have been reported to influence conscious perception. It is not clear whether these effects are distinct or related phenomena, or whether they are early sensory effects or late decisional processes. Combining electroencephalography and electrocardiography, along with signal detection theory analyses, we identify two distinct heartbeat-related influences on conscious perception differentially related to early vs. late somatosensory processing. First, an effect on early sensory processing was found for the heartbeat-evoked potential (HEP), a marker of cardiac interoception. The amplitude of the prestimulus HEP negatively correlated with localization and detection of somatosensory stimuli, reflecting a more conservative detection bias (criterion). Importantly, higher HEP amplitudes were followed by decreases in early (P50) as well as late (N140, P300) somatosensoryevoked potential (SEP) amplitudes. Second, stimulus timing along the cardiac cycle also affected perception. During systole, stimuli were detected and correctly localized less frequently, relating to a shift in perceptual sensitivity. This perceptual attenuationwas accompanied by the suppression of only late SEP components (P300) and was stronger for individuals with a more stable heart rate. Both heart-related effects were independent of alpha oscillations’ influence on somatosensory processing. We explain cardiac cycle timing effects in a predictive coding account and suggest that HEP-related effects might reflect spontaneous shifts between interoception and exteroception or modulations of general attentional resources. Thus, our results provide a general conceptual framework to explain how internal signals can be integrated into our conscious perception of the world.

•Electrical stimulation provides cortical activation comparable to fMRI studies.•Vibrotactile stimulation elicits more complex connectivity and processing.•Electrical stimulation ensures a more accurate finger mapping within S1.•High-frequency vibrotactile stimulation shows promise for finger mapping. Somatosensory evoked potentials (SEPs) recorded with electroencephalography offer insights into cortical responses to tactile stimulation, typically elicited through temporally precise electrical stimulation. Although vibrotactile stimulation is more ecologically valid but less common, studies directly comparing EEG responses to both electrical and vibrotactile finger stimulation are limited. This study examines and compares (a) cortical responses, (b) connectivity patterns, and (c) somatotopic accuracy of these stimulation types on the fingers. In two experiments, SEPs were recorded from healthy participants’ right-hand finger stimulation, using either electrical (experiment 1, n = 22) or vibrotactile (experiment 2, n = 22) stimulation. Vibrotactile stimuli were delivered at 10, 50, and 250 Hz, targeting different ranges of tactile mechanoreceptors activations. Electrical stimulation reliability was assessed across two days, showing consistent SEP amplitudes and latencies. Both stimulation types generated three early components (P1, N1, P2), but all vibrotactile components were increasingly delayed compared to electrical stimulation. Vibrotactile stimulation exhibited stronger localized connectivity in early components (P1, N1) in the left hemisphere, while electrical stimulation showed broader connectivity at P2. Electrical stimulation provided a clearer somatotopic organization in the postcentral gyrus than vibrotactile stimulation. These findings suggest distinct processing for electrical versus vibrotactile finger stimulation. These two stimulation methods are not interchangeable in somatosensory studies: the temporal shift in vibrotactile responses reflects selective activation of Pacinian corpuscles, whereas electrical stimulation yields stronger generalized cortical processing. Electrical stimulation may engage a serial processing pathway starting in the primary somatosensory cortex, while vibrotactile stimulation could involve parallel processing in both primary and secondary somatosensory cortices.

Topographic sensory maps are a prominent feature of the adult primate brain. Here, we asked whether topographic representations of the body are present at birth. Using functional MRI (fMRI), we find that the newborn somatomotor system, spanning frontoparietal cortex and subcortex, comprises multiple topographic representations of the body. The organization of these large-scale body maps was indistinguishable from those in older monkeys. Finer-scale differentiation of individual fingers increased over the first 2 y, suggesting that topographic representations are refined during early development. Last, we found that somatomotor representations were unchanged in 2 visually impaired monkeys who relied on touch for interacting with their environment, demonstrating that massive shifts in early sensory experience in an otherwise anatomically intact brain are insufficient for driving cross-modal plasticity. We propose that a topographic scaffolding is present at birth that both directs and constrains experience-driven modifications throughout somatosensory and motor systems.

Transcranial alternating current stimulation (tACS) modulates brain activity by passing electrical current through electrodes that are attached to the scalp. Because it is safe and noninvasive, tACS holds great promise as a tool for basic research and clinical treatment. However, little is known about how tACS ultimately influences neural activity. One hypothesis is that tACS affects neural responses directly, by producing electrical fields that interact with the brain's endogenous electrical activity. By controlling the shape and location of these electric fields, one could target brain regions associated with particular behaviors or symptoms. However, an alternative hypothesis is that tACS affects neural activity indirectly, via peripheral sensory afferents. In particular, it has often been hypothesized that tACS acts on sensory fibers in the skin, which in turn provide rhythmic input to central neurons. In this case, there would be little possibility of targeted brain stimulation, as the regions modulated by tACS would depend entirely on the somatosensory pathways originating in the skin around the stimulating electrodes. Here, we directly test these competing hypotheses by recording single-unit activity in the hippocampus and visual cortex of alert monkeys receiving tACS. We find that tACS entrains neuronal activity in both regions, so that cells fire synchronously with the stimulation. Blocking somatosensory input with a topical anesthetic does not significantly alter these neural entrainment effects. These data are therefore consistent with the direct stimulation hypothesis and suggest that peripheral somatosensory stimulation is not required for tACS to entrain neurons.

Integrating artificial limbs as part of one's body involves complex neuroplastic changes resulting from various sensory inputs. While somatosensory feedback is crucial, plastic processes that enable embodiment remain unknown. We investigated this using somatosensory evoked fields (SEFs) in the primary somatosensory cortex (S1) following the Rubber Hand Illusion (RHI), known to quickly induce artificial limb embodiment. During electrical stimulation of the little finger and thumb, 19 adults underwent neuromagnetic recordings before and after the RHI. We found early SEF displacement, including an illusion-brain correlation between extent of embodiment and specific changes to the first cortical response at 20 ms in Area 3b, within S1. Furthermore, we observed a posteriorly directed displacement at 35 ms towards Area 1, known to be important for visual integration during touch perception. That this second displacement was unrelated to extent of embodiment implies a functional distinction between neuroplastic changes of these components and areas. The earlier shift in Area 3b may shape extent of limb ownership, while subsequent displacement into Area 1 may relate to early visual-tactile integration that initiates embodiment. Here we provide evidence for multiple neuroplastic processes in S1—lasting beyond the illusion—supporting integration of artificial limbs like prostheses within the body representation.

Viral infection during pregnancy is correlated with increased frequency of neurodevelopmental disorders, and this is studied in mice prenatally subjected to maternal immune activation (MIA). We previously showed that maternal T helper 17 cells promote the development of cortical and behavioural abnormalities in MIA-affected offspring. Here we show that cortical abnormalities are preferentially localized to a region encompassing the dysgranular zone of the primary somatosensory cortex (S1DZ). Moreover, activation of pyramidal neurons in this cortical region was sufficient to induce MIA-associated behavioural phenotypes in wild-type animals, whereas reduction in neural activity rescued the behavioural abnormalities in MIA-affected offspring. Sociability and repetitive behavioural phenotypes could be selectively modulated according to the efferent targets of S1DZ. Our work identifies a cortical region primarily, if not exclusively, centred on the S1DZ as the major node of a neural network that mediates behavioural abnormalities observed in offspring exposed to maternal inflammation. The authors define a specific cortical subregion of the somatosensory cortex as a critical region of dysfunction that is causal to the emergence of abnormal social and repetitive behaviours in mice exposed to maternal inflammation. Brain patches behind behavioural defects Viral infection and activation of the maternal immune system (MIA) during pregnancy has been linked to behavioural abnormalities in the offspring. In this study, Gloria Choi, Jun Huh and colleagues identify a specific cortical subregion of the somatosensory cortex as a critical region of dysfunction, and show that the presence and size of cortical patches correlate with specific social behaviours. In a related paper published this week, Gloria Choi, Jun Huh and colleagues provide evidence that MIA-mediated abnormal behavioural phenotypes require defined gut commensal bacteria for the induction of interleukin-17 (IL-17)-producing T helper 17 (T H 17) cells, in accordance with previous studies that have demonstrated a role in this association.

Two largely distinct bodies of research have demonstrated age-related alterations and disease-specific aberrations in both local gamma oscillations and patterns of cortical thickness. However, seldom has the relationship between gamma activity and cortical thickness been investigated. Herein, we combine the spatiotemporal precision of magnetoencephalography (MEG) with high-resolution magnetic resonance imaging and surface-based morphometry to characterize the relationships between somatosensory gamma oscillations and the thickness of the cortical tissue generating the oscillations in 94 healthy adults (age range: 22–72). Specifically, a series of regressions were computed to assess the relationships between thickness of the primary somatosensory cortex (S1), S1 gamma response power, peak gamma frequency, and somatosensory gating of identical stimuli. Our results indicated that increased S1 thickness significantly predicted greater S1 gamma response power, reduced peak gamma frequency, and improved somatosensory gating. Furthermore, peak gamma frequency significantly and partially mediated the relationship between S1 thickness and the magnitude of the S1 gamma response. Finally, advancing age significantly predicted reduced S1 thickness and decreased gating of redundant somatosensory stimuli. Notably, this is the first study to directly link somatosensory gamma oscillations to local cortical thickness. Our results demonstrate a multi-faceted relationship between structure and function, and have important implications for understanding age- and disease-related deficits in basic sensory processing and higher-order inhibitory function. •Possible links between local cortical thickness and gamma-band activity are unclear.•Adults underwent structural MRI and a somatosensory gating task during MEG.•Advanced oscillatory and surface-based morphometry analysis methods were combined.•Local cortical thickness predicted gamma response power, frequency, and gating.•Peak gamma frequency mediated the relationship between thickness and response power.

•We investigated the contribution of somatosensory system in object perception.•Tactile probes were coupled with affordable/non-affordable objects images.•Viewing graspable objects enhances somatosensory activity to concurrent tactile input.•Findings support the role of somatosensory system in affordance processing. Object perception is inherently multisensory, as the brain integrates information across sensory modalities to facilitate the interaction with them. This intrinsic ‘action potential’ of objects is described by the concept of affordance, which refers to the opportunities for interaction that an object offers to an organism, depending on both the object’s physical characteristics and the organism’s sensorimotor abilities. Converging evidence demonstrated that seeing affordable objects modulates motor activity. Coherently, viewing graspable objects can also induce a somatosensory activation associated with their tactile manipulation. Yet, little is known about the representation of affordances in the somatosensory system. Here, we investigated whether visual perception of affordable objects modulates somatosensory evoked activity. Participants viewed images of affordable and non-affordable objects, while concomitantly probing the somatosensory system with tactile stimuli delivered to both index fingers. We found that viewing graspable objects enhances somatosensory processing, as indicated by higher somatosensory evoked potentials to tactile stimuli when paired with images of affordable objects compared to non-affordable objects. These findings suggest that the observation of affordable objects triggers somatosensory responses associated with potential actions, supporting the view that object perception is a dynamic multisensory process. In everyday interactions, objects like cups are consistently grasped, leading to the formation of strong multisensory associations between objects’ visual features and tactile afferences. Once well-established, these associations may allow vision alone to activate stored tactile representations, enhancing somatosensory engagement, as observed in our study.

Non-pial neocortical astrocytes have historically been thought to comprise largely a nondiverse population of protoplasmic astrocytes. Here we show that astrocytes of the mouse somatosensory cortex manifest layer-specific morphological and molecular differences. Two- and three-dimensional observations revealed that astrocytes in the different layers possess distinct morphologies as reflected by differences in cell orientation, territorial volume, and arborization. The extent of ensheathment of synaptic clefts by astrocytes in layer II/III was greater than that by those in layer VI. Moreover, differences in gene expression were observed between upper-layer and deep-layer astrocytes. Importantly, layer-specific differences in astrocyte properties were abrogated in reeler and Dab1 conditional knockout mice, in which neuronal layers are disturbed, suggesting that neuronal layers are a prerequisite for the observed morphological and molecular differences of neocortical astrocytes. This study thus demonstrates the existence of layer-specific interactions between neurons and astrocytes, which may underlie their layer-specific functions. Several studies have suggested that astrocytes in the neocortex are more diverse than previously thought. Here, the authors describe layer-specific differences in morphology and molecular characteristics of astrocytes that depend on the neurons within those layers.