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Two dynamically distinct circuits driving inhibition in sensory thalamus

Most sensory information destined for the neocortex is relayed through the thalamus, where considerable transformation occurs(1,2). One powerful means of transformation involves interactions between excitatory thalamocortical neurons that carry data to cortex and inhibitory neurons of the thalamic r...

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Autores principales: Martinez-Garcia, Rosa I., Voelcker, Bettina, Zaltsman, Julia B., Patrick, Saundra L., Stevens, Tanya R., Connors, Barry W., Cruikshank, Scott J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394732/
https://www.ncbi.nlm.nih.gov/pubmed/32699410
http://dx.doi.org/10.1038/s41586-020-2512-5
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author Martinez-Garcia, Rosa I.
Voelcker, Bettina
Zaltsman, Julia B.
Patrick, Saundra L.
Stevens, Tanya R.
Connors, Barry W.
Cruikshank, Scott J.
author_facet Martinez-Garcia, Rosa I.
Voelcker, Bettina
Zaltsman, Julia B.
Patrick, Saundra L.
Stevens, Tanya R.
Connors, Barry W.
Cruikshank, Scott J.
author_sort Martinez-Garcia, Rosa I.
collection PubMed
description Most sensory information destined for the neocortex is relayed through the thalamus, where considerable transformation occurs(1,2). One powerful means of transformation involves interactions between excitatory thalamocortical neurons that carry data to cortex and inhibitory neurons of the thalamic reticular nucleus (TRN) that regulate flow of those data(3–6). Despite enduring recognition of its importance(7–9), understanding of TRN cell types, their organization, and their functional properties has lagged that of the thalamocortical systems they control. Here we address this, investigating somatosensory and visual circuits of the TRN. In the somatosensory TRN we observed two groups of genetically defined neurons that are topographically segregated, physiologically distinct, and connect reciprocally with independent thalamocortical nuclei via dynamically divergent synapses. Calbindin-expressing cells, located in the central core, connect with the ventral posterior nucleus (VP), the primary somatosensory thalamocortical relay. In contrast, somatostatin-expressing cells, residing along the surrounding edges of TRN, synapse with the posterior medial thalamic nucleus (POM), a higher-order structure that carries both top-down and bottom-up information(10–12). The two TRN cell groups process their inputs in pathway-specific ways. Synapses from VP to central TRN cells transmit rapid excitatory currents that depress deeply during repetitive activity, driving phasic spike output. Synapses from POM to edge TRN cells evoke slower, less depressing excitatory currents that drive more persistent spiking. Differences in intrinsic physiology of TRN cell types, including state-dependent bursting, contribute to these output dynamics. Thus, processing specializations of two somatosensory TRN subcircuits appear to be tuned to the signals they carry—a primary central subcircuit to discrete sensory events, and a higher-order edge subcircuit to temporally distributed signals integrated from multiple sources. The structure and function of visual TRN subcircuits closely resemble those of the somatosensory TRN. These results provide fundamental insights about how subnetworks of TRN neurons may differentially process distinct classes of thalamic information.
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spelling pubmed-73947322021-01-22 Two dynamically distinct circuits driving inhibition in sensory thalamus Martinez-Garcia, Rosa I. Voelcker, Bettina Zaltsman, Julia B. Patrick, Saundra L. Stevens, Tanya R. Connors, Barry W. Cruikshank, Scott J. Nature Article Most sensory information destined for the neocortex is relayed through the thalamus, where considerable transformation occurs(1,2). One powerful means of transformation involves interactions between excitatory thalamocortical neurons that carry data to cortex and inhibitory neurons of the thalamic reticular nucleus (TRN) that regulate flow of those data(3–6). Despite enduring recognition of its importance(7–9), understanding of TRN cell types, their organization, and their functional properties has lagged that of the thalamocortical systems they control. Here we address this, investigating somatosensory and visual circuits of the TRN. In the somatosensory TRN we observed two groups of genetically defined neurons that are topographically segregated, physiologically distinct, and connect reciprocally with independent thalamocortical nuclei via dynamically divergent synapses. Calbindin-expressing cells, located in the central core, connect with the ventral posterior nucleus (VP), the primary somatosensory thalamocortical relay. In contrast, somatostatin-expressing cells, residing along the surrounding edges of TRN, synapse with the posterior medial thalamic nucleus (POM), a higher-order structure that carries both top-down and bottom-up information(10–12). The two TRN cell groups process their inputs in pathway-specific ways. Synapses from VP to central TRN cells transmit rapid excitatory currents that depress deeply during repetitive activity, driving phasic spike output. Synapses from POM to edge TRN cells evoke slower, less depressing excitatory currents that drive more persistent spiking. Differences in intrinsic physiology of TRN cell types, including state-dependent bursting, contribute to these output dynamics. Thus, processing specializations of two somatosensory TRN subcircuits appear to be tuned to the signals they carry—a primary central subcircuit to discrete sensory events, and a higher-order edge subcircuit to temporally distributed signals integrated from multiple sources. The structure and function of visual TRN subcircuits closely resemble those of the somatosensory TRN. These results provide fundamental insights about how subnetworks of TRN neurons may differentially process distinct classes of thalamic information. 2020-07-22 2020-07 /pmc/articles/PMC7394732/ /pubmed/32699410 http://dx.doi.org/10.1038/s41586-020-2512-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Martinez-Garcia, Rosa I.
Voelcker, Bettina
Zaltsman, Julia B.
Patrick, Saundra L.
Stevens, Tanya R.
Connors, Barry W.
Cruikshank, Scott J.
Two dynamically distinct circuits driving inhibition in sensory thalamus
title Two dynamically distinct circuits driving inhibition in sensory thalamus
title_full Two dynamically distinct circuits driving inhibition in sensory thalamus
title_fullStr Two dynamically distinct circuits driving inhibition in sensory thalamus
title_full_unstemmed Two dynamically distinct circuits driving inhibition in sensory thalamus
title_short Two dynamically distinct circuits driving inhibition in sensory thalamus
title_sort two dynamically distinct circuits driving inhibition in sensory thalamus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394732/
https://www.ncbi.nlm.nih.gov/pubmed/32699410
http://dx.doi.org/10.1038/s41586-020-2512-5
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