NMDA receptors control development of somatosensory callosal axonal projections

Callosal projections from primary somatosensory cortex (S1) are key for processing somatosensory inputs and integrating sensory-motor information. How the callosal innervation pattern in S1 is formed during early postnatal development is not clear. We found that the normal termination pattern of the...

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Main Authors: Jing Zhou, Yong Lin, Trung Huynh, Hirofumi Noguchi, Jeffrey O Bush, Samuel J Pleasure
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-03-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/59612
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spelling doaj-a939c38ac0644da580c581751482322e2021-05-05T22:51:44ZengeLife Sciences Publications LtdeLife2050-084X2021-03-011010.7554/eLife.59612NMDA receptors control development of somatosensory callosal axonal projectionsJing Zhou0https://orcid.org/0000-0003-2809-7097Yong Lin1Trung Huynh2Hirofumi Noguchi3https://orcid.org/0000-0002-9779-4956Jeffrey O Bush4https://orcid.org/0000-0002-6053-8756Samuel J Pleasure5https://orcid.org/0000-0001-8599-1613Department of Neurology, University of California, San Francisco, San Francisco, United States; Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, United StatesDepartment of Neurology, University of California, San Francisco, San Francisco, United States; Department of Neurological Surgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Neurology, University of California, San Francisco, San Francisco, United States; Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, United StatesDepartment of Neurology, University of California, San Francisco, San Francisco, United States; Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, United StatesDepartment of Cell and Tissue Biology, Program in Craniofacial Biology and Institute for Human Genetics, University of California, San Francisco, San Francisco, United States; Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, United StatesDepartment of Neurology, University of California, San Francisco, San Francisco, United States; Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, United States; Programs in Neuroscience and Developmental Stem Cell Biology, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Kavli Institute for Fundamental Neuroscience, San Francisco, United StatesCallosal projections from primary somatosensory cortex (S1) are key for processing somatosensory inputs and integrating sensory-motor information. How the callosal innervation pattern in S1 is formed during early postnatal development is not clear. We found that the normal termination pattern of these callosal projections is disrupted in cortex specific NMDAR mutants. Rather than projecting selectively to the primary/secondary somatosensory cortex (S1/S2) border, axons were uniformly distributed throughout S1. In addition, the density of this projection increased over postnatal life until the mice died by P30. By combining genetic and antibody-mediated loss of function, we demonstrated that it is GluN2B-containing NMDA receptors in target S1 that mediate this guidance phenotype, thus playing a central role in interhemispheric connectivity. Furthermore, we found that this function of NMDA receptors in callosal circuit formation is independent of ion channel function and works with the EPHRIN-B/EPHB system. Thus, NMDAR in target S1 cortex regulates the formation callosal circuits perhaps by modulating EPH-dependent repulsion.https://elifesciences.org/articles/59612axon guidancecorpus callosumsomatosensory cortex
collection DOAJ
language English
format Article
sources DOAJ
author Jing Zhou
Yong Lin
Trung Huynh
Hirofumi Noguchi
Jeffrey O Bush
Samuel J Pleasure
spellingShingle Jing Zhou
Yong Lin
Trung Huynh
Hirofumi Noguchi
Jeffrey O Bush
Samuel J Pleasure
NMDA receptors control development of somatosensory callosal axonal projections
eLife
axon guidance
corpus callosum
somatosensory cortex
author_facet Jing Zhou
Yong Lin
Trung Huynh
Hirofumi Noguchi
Jeffrey O Bush
Samuel J Pleasure
author_sort Jing Zhou
title NMDA receptors control development of somatosensory callosal axonal projections
title_short NMDA receptors control development of somatosensory callosal axonal projections
title_full NMDA receptors control development of somatosensory callosal axonal projections
title_fullStr NMDA receptors control development of somatosensory callosal axonal projections
title_full_unstemmed NMDA receptors control development of somatosensory callosal axonal projections
title_sort nmda receptors control development of somatosensory callosal axonal projections
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2021-03-01
description Callosal projections from primary somatosensory cortex (S1) are key for processing somatosensory inputs and integrating sensory-motor information. How the callosal innervation pattern in S1 is formed during early postnatal development is not clear. We found that the normal termination pattern of these callosal projections is disrupted in cortex specific NMDAR mutants. Rather than projecting selectively to the primary/secondary somatosensory cortex (S1/S2) border, axons were uniformly distributed throughout S1. In addition, the density of this projection increased over postnatal life until the mice died by P30. By combining genetic and antibody-mediated loss of function, we demonstrated that it is GluN2B-containing NMDA receptors in target S1 that mediate this guidance phenotype, thus playing a central role in interhemispheric connectivity. Furthermore, we found that this function of NMDA receptors in callosal circuit formation is independent of ion channel function and works with the EPHRIN-B/EPHB system. Thus, NMDAR in target S1 cortex regulates the formation callosal circuits perhaps by modulating EPH-dependent repulsion.
topic axon guidance
corpus callosum
somatosensory cortex
url https://elifesciences.org/articles/59612
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AT yonglin nmdareceptorscontroldevelopmentofsomatosensorycallosalaxonalprojections
AT trunghuynh nmdareceptorscontroldevelopmentofsomatosensorycallosalaxonalprojections
AT hirofuminoguchi nmdareceptorscontroldevelopmentofsomatosensorycallosalaxonalprojections
AT jeffreyobush nmdareceptorscontroldevelopmentofsomatosensorycallosalaxonalprojections
AT samueljpleasure nmdareceptorscontroldevelopmentofsomatosensorycallosalaxonalprojections
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