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Anibal-Martinez, M.

Publications and source records attributed to Anibal-Martinez, M..

2 recordsLinked to original sources

Combinatorial Cell-Adhesion and Activity Codes Instruct Cortical Modality Identity

The emergence of functional sensory modalities requires precise cortical arealization and appropriate thalamocortical targeting. Although early morphogen gradients set broad cortical territories, the mechanisms that specify sensory identity and guide modality-specific thalamocortical targeting remain unknown. Here, we identify an embryonic set of activity-independent cortical "protogenes", prominently enriched for cell-adhesion molecules, that are differentially expressed between primary somatosensory (S1) and visual (V1) cortices prior to thalamic innervation. These adhesion programs are selectively localized to layer 4, the main thalamo-recipient layer, and strikingly mirror the adhesion profiles of their corresponding thalamic nuclei, suggesting partner recognition. Disrupting thalamic activity alters modality-specific spontaneous cortical dynamics and the postnatal expression of another set of modality-specific genes, indicating a modulatory role for thalamic activity in cortical identity. These findings support a two-step model in which cortical identity is primed by adhesion codes driving modality-specific thalamocortical targeting, and later refined by patterned thalamic activity to establish functional cortical modalities.

neuroscience↗

Prenatal tuning of thalamic spontaneous activity patterns regulates somatosensory map resolution

Precise mapping of peripheral inputs onto cortical areas is required for appropriate sensory processing. In the mouse primary somatosensory cortex, mystacial whiskers are represented in large barrels, while upper lip whiskers are in smaller, less defined barrels. Barrel size and definition of these two functionally distinct barrel maps are believed to be determined by the type of whisker input and peripheral receptor density. However, spontaneous activity and transcriptional programs at prenatal developmental stages can influence somatosensory map development independently of sensory experience. Thus, the mechanisms defining distinct barrel field territories, including their size and definition, remain poorly understood. Here, we show that prenatal ablation of mystacial whiskers remap somatosensory cortical territories resulting in enhancement of the functional and anatomical definition of upper lip whisker barrels. These changes do not result from alterations in receptor type but rather stem from thalamic upper lip input-receiving neurons adopting a mystacial-like transcriptional profile. Our results unveil a regulated prenatal mechanism within the thalamus that maps available somatosensory input to ensure sufficient cortical barrel size and functional spatial resolution for sensory processing, irrespective of peripheral receptor type and density.

neuroscience↗