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Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period
The lateral cortex of the inferior colliculus (LCIC) is a multimodal subdivision of the midbrain inferior colliculus (IC) that plays a key role in sensory integration. The LCIC is compartmentally-organized, exhibiting a series of discontinuous patches or modules surrounded by an extramodular matrix....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021614/ https://www.ncbi.nlm.nih.gov/pubmed/35463204 http://dx.doi.org/10.3389/fncir.2022.882485 |
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author | Weakley, Jacob M. Kavusak, Erin K. Carroll, Julianne B. Gabriele, Mark L. |
author_facet | Weakley, Jacob M. Kavusak, Erin K. Carroll, Julianne B. Gabriele, Mark L. |
author_sort | Weakley, Jacob M. |
collection | PubMed |
description | The lateral cortex of the inferior colliculus (LCIC) is a multimodal subdivision of the midbrain inferior colliculus (IC) that plays a key role in sensory integration. The LCIC is compartmentally-organized, exhibiting a series of discontinuous patches or modules surrounded by an extramodular matrix. In adult mice, somatosensory afferents target LCIC modular zones, while auditory afferents terminate throughout the encompassing matrix. Recently, we defined an early LCIC critical period (birth: postnatal day 0 to P12) based upon the concurrent emergence of its neurochemical compartments (modules: glutamic acid decarboxylase, GAD+; matrix: calretinin, CR+), matching Eph-ephrin guidance patterns, and specificity of auditory inputs for its matrix. Currently lacking are analogous experiments that address somatosensory afferent shaping and the construction of discrete LCIC multisensory maps. Combining living slice tract-tracing and immunocytochemical approaches in a developmental series of GAD67-GFP knock-in mice, the present study characterizes: (1) the targeting of somatosensory terminals for emerging LCIC modular fields; and (2) the relative separation of somatosensory and auditory inputs over the course of its established critical period. Results indicate a similar time course and progression of LCIC projection shaping for both somatosensory (corticocollicular) and auditory (intracollicular) inputs. While somewhat sparse and intermingling at birth, modality-specific projection patterns soon emerge (P4–P8), coincident with peak guidance expression and the appearance of LCIC compartments. By P12, an adult-like arrangement is in place, with fully segregated multimodal afferent arrays. Quantitative measures confirm increasingly distinct input maps, exhibiting less projection overlap with age. Potential mechanisms whereby multisensory LCIC afferent systems recognize and interface with its emerging modular-matrix framework are discussed. |
format | Online Article Text |
id | pubmed-9021614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90216142022-04-22 Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period Weakley, Jacob M. Kavusak, Erin K. Carroll, Julianne B. Gabriele, Mark L. Front Neural Circuits Neuroscience The lateral cortex of the inferior colliculus (LCIC) is a multimodal subdivision of the midbrain inferior colliculus (IC) that plays a key role in sensory integration. The LCIC is compartmentally-organized, exhibiting a series of discontinuous patches or modules surrounded by an extramodular matrix. In adult mice, somatosensory afferents target LCIC modular zones, while auditory afferents terminate throughout the encompassing matrix. Recently, we defined an early LCIC critical period (birth: postnatal day 0 to P12) based upon the concurrent emergence of its neurochemical compartments (modules: glutamic acid decarboxylase, GAD+; matrix: calretinin, CR+), matching Eph-ephrin guidance patterns, and specificity of auditory inputs for its matrix. Currently lacking are analogous experiments that address somatosensory afferent shaping and the construction of discrete LCIC multisensory maps. Combining living slice tract-tracing and immunocytochemical approaches in a developmental series of GAD67-GFP knock-in mice, the present study characterizes: (1) the targeting of somatosensory terminals for emerging LCIC modular fields; and (2) the relative separation of somatosensory and auditory inputs over the course of its established critical period. Results indicate a similar time course and progression of LCIC projection shaping for both somatosensory (corticocollicular) and auditory (intracollicular) inputs. While somewhat sparse and intermingling at birth, modality-specific projection patterns soon emerge (P4–P8), coincident with peak guidance expression and the appearance of LCIC compartments. By P12, an adult-like arrangement is in place, with fully segregated multimodal afferent arrays. Quantitative measures confirm increasingly distinct input maps, exhibiting less projection overlap with age. Potential mechanisms whereby multisensory LCIC afferent systems recognize and interface with its emerging modular-matrix framework are discussed. Frontiers Media S.A. 2022-04-07 /pmc/articles/PMC9021614/ /pubmed/35463204 http://dx.doi.org/10.3389/fncir.2022.882485 Text en Copyright © 2022 Weakley, Kavusak, Carroll and Gabriele. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Weakley, Jacob M. Kavusak, Erin K. Carroll, Julianne B. Gabriele, Mark L. Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period |
title | Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period |
title_full | Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period |
title_fullStr | Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period |
title_full_unstemmed | Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period |
title_short | Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period |
title_sort | segregation of multimodal inputs into discrete midbrain compartments during an early critical period |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021614/ https://www.ncbi.nlm.nih.gov/pubmed/35463204 http://dx.doi.org/10.3389/fncir.2022.882485 |
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