Evidence map›Paper›PMID 33661095›Full record

ArticleeLife2021

NMDA receptors control development of somatosensory callosal axonal projections.

Jing Zhou, Yong Lin, Trung Huynh, Hirofumi Noguchi, Jeffrey O Bush, Samuel J Pleasure

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  4. Mef2c Controls Postnatal Callosal Axon Targeting by Regulating Sensitivity to Ephrin Repulsion.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  8. Article
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  11. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Jing ZhouDepartment of Neurology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0003-2809-7097
Yong LinDepartment of Neurology, University of California, San Francisco, San Francisco, United States.
Trung HuynhDepartment of Neurology, University of California, San Francisco, San Francisco, United States.
Hirofumi NoguchiDepartment of Neurology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0002-9779-4956
Jeffrey O BushDepartment of Cell and Tissue Biology, Program in Craniofacial Biology and Institute for Human Genetics, University of California, San Francisco, San Francisco, United States.ORCID 0000-0002-6053-8756
Samuel J PleasureDepartment of Neurology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0001-8599-1613
University of California, San Francisco · US

Funding

Autoimmune Encephalitis - Ataxia and Psychiatric Disease: Identifying and Characterizing Novel Antibody TargetsR01MH122471 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOSEPH L. DERISI, SAMUEL JEREMY PLEASURE · 2020 to 2026
$4.7M
Mechanisms of Eph/Ephrin signaling in craniofacial morphogenesis and craniofrontonasal syndromeR01DE023337 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BUSH, JEFFREY OHMANN · 2013 to 2021
$4.3M
NMDA receptors and callosal circuitry: development and molecular mechanismsR01MH119435 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PLEASURE, SAMUEL JEREMY · 2020 to 2023
$1.6M
NMDA receptors and callosal circuitry: development and molecular mechanismsR56MH119435 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PLEASURE, SAMUEL JEREMY · 2019 to 2019
$401k
NIDCR NIH HHS R01 DE023337NIMH NIH HHS R01 MH119435NIMH NIH HHS R01 MH122471NIMH NIH HHS R56 MH119435
6 · The paper itself

Abstract

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.

Indexed as

AnimalsAxonsCorpus CallosumFemaleMaleMiceReceptors, N-Methyl-D-AspartateSomatosensory CortexNR2B NMDA receptorReceptors, N-Methyl-D-Aspartateaxon guidancecorpus callosumdevelopmental biologymouseneurosciencesomatosensory cortex

Identifiers

PMID33661095
PMCPMC7959694
OpenAlexW3134381812

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.