RESUMEN
A fundamental paradigm in neuroscience is the concept of neural coding through tuning functions 1 . According to this idea, neurons encode stimuli through fixed mappings of stimulus features to firing rates. Here, we report that the tuning of visual neurons can rapidly and coherently change across a population to attend to a whole and its parts. We set out to investigate a longstanding debate concerning whether inferotemporal (IT) cortex uses a specialized code for representing specific types of objects or whether it uses a general code that applies to any object. We found that face cells in macaque IT cortex initially adopted a general code optimized for face detection. But following a rapid, concerted population event lasting < 20 ms, the neural code transformed into a face-specific one with two striking properties: (i) response gradients to principal detection-related dimensions reversed direction, and (ii) new tuning developed to multiple higher feature space dimensions supporting fine face discrimination. These dynamics were face specific and did not occur in response to objects. Overall, these results show that, for faces, face cells shift from detection to discrimination by switching from an object-general code to a face-specific code. More broadly, our results suggest a novel mechanism for neural representation: concerted, stimulus-dependent switching of the neural code used by a cortical area.
RESUMEN
The thalamic reticular nucleus (TRN), the major source of thalamic inhibition, regulates thalamocortical interactions that are critical for sensory processing, attention and cognition1-5. TRN dysfunction has been linked to sensory abnormality, attention deficit and sleep disturbance across multiple neurodevelopmental disorders6-9. However, little is known about the organizational principles that underlie its divergent functions. Here we performed an integrative study linking single-cell molecular and electrophysiological features of the mouse TRN to connectivity and systems-level function. We found that cellular heterogeneity in the TRN is characterized by a transcriptomic gradient of two negatively correlated gene-expression profiles, each containing hundreds of genes. Neurons in the extremes of this transcriptomic gradient express mutually exclusive markers, exhibit core or shell-like anatomical structure and have distinct electrophysiological properties. The two TRN subpopulations make differential connections with the functionally distinct first-order and higher-order thalamic nuclei to form molecularly defined TRN-thalamus subnetworks. Selective perturbation of the two subnetworks in vivo revealed their differential role in regulating sleep. In sum, our study provides a comprehensive atlas of TRN neurons at single-cell resolution and links molecularly defined subnetworks to the functional organization of thalamocortical circuits.
