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Campos-Perez, A. F.

Publications and source records attributed to Campos-Perez, A. F..

2 recordsLinked to original sources

Multiple task-demands flexibly optimize neural geometry in human ventral temporal cortex

A hallmark of human intelligence is the ability to perform multiple tasks immediately upon instruction. Yet, the neural processes that implement such flexibility remain unclear. Using intracranial electrophysiology in epilepsy patients, we examined how representational geometries evolve as participants switched among three tasks - individuation, categorization, and conceptualization - on a trial-by-trial basis. Although tasks differed in the required representational geometries, neural representations across cortex were not immediately optimized following task cues. Instead, task-tailored geometries emerged gradually over successive stimulus repetitions within a trial. Ventral temporal cortex was the only region to exhibit task-specific adjustments for all three tasks, dynamically transforming within- and between-category distances in line with task demands. Importantly, these gradual representational changes were behaviorally relevant, predicting trial-level performance. Our results show that behavioral flexibility is supported by incremental, task-dependent refinement of representational geometry already within sensory cortex - far earlier in the processing hierarchy than previously thought.

neuroscience↗

Lack of evidence for participation of TMEM150c/TENTONIN3 in sensory mechanotransduction.

The membrane protein TMEM150c has been proposed to form a mechanosensitive ion channel that is required for normal proprioceptor function. Here we examined whether expression of TMEM150c in neuroblastoma cells lacking Piezo1 is associated with the appearance of mechanosensitive currents. Using three different modes of mechanical stimuli, indentation, membrane stretch and substrate deflection we could not evoke mechanosensitive currents in cells expressing TMEM150c. We next asked if TMEM150c is necessary for the normal mechanosensitivity of cutaneous sensory neurons. We used an available mouse model in which the Tmem150c locus was disrupted through the insertion of a LacZ cassette with a splice acceptor that should lead to transcript truncation. Analysis of these mice indicated that ablation of the Tmem150c gene was not complete in sensory neurons of the dorsal root ganglia (DRG). Using a Crispr/cas9 strategy we made a second mouse model in which a large part of the Tmem150c gene was deleted and established that these Tmem150c-/- mice completely lack TMEM150c protein in the DRGs. We used an ex vivo skin nerve preparation to characterize the mechanosenstivity of mechanoreceptors and nociceptors in the glabrous skin of the Tmem150c-/- mice. We found no quantitative alterations in the physiological properties of any type of cutaneous sensory fiber in Tmem150c-/- mice. Since it has been claimed that TMEM150c is required for normal proprioceptor function we made a quantitative analysis of locomotion in Tmem150c-/- mice. Here again we found no indication that there was altered gait in Tmem150c-/- mice compared to wild type controls. In summary, we conclude that existing mouse models that have been used to investigate TMEM150c function in vivo are problematic. Furthermore, we could find no evidence that TMEM150c forms a mechanosensitive channel or that it is necessary for the normal mechanosensitivity of cutaneous sensory neurons.

neuroscience↗