Evidence map›Paper›PMID 38585721›Full record

ArticlebioRxiv : the preprint server for biology2024

Symmetry in levels of axon-axon homophilic adhesion establishes topography in the corpus callosum and development of connectivity between brain hemispheres.

Alexandros Poulopoulos, Patrick Davis, Cheryl Brandenburg, Yasuhiro Itoh, Maria J Galazo, Luciano C Greig, Andrea J Romanowski, Bogdan Budnik, Jeffrey D Macklis

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 11 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 2 institutions in 1 country.

Alexandros PoulopoulosDepartment of Stem Cell and Regenerative Biology, and Center for Brain Science, Harvard University, Cambridge, MA, USA.ORCID 0000-0002-5318-7388
Patrick DavisDepartment of Stem Cell and Regenerative Biology, and Center for Brain Science, Harvard University, Cambridge, MA, USA.ORCID 0000-0003-0913-7030
Cheryl BrandenburgUniversity of Maryland School of Medicine, Department of Pharmacology, Baltimore, MD, USA.ORCID 0000-0002-9370-2313
Yasuhiro ItohDepartment of Stem Cell and Regenerative Biology, and Center for Brain Science, Harvard University, Cambridge, MA, USA.ORCID 0000-0001-8590-9122
Maria J GalazoDepartment of Stem Cell and Regenerative Biology, and Center for Brain Science, Harvard University, Cambridge, MA, USA.ORCID 0000-0003-1909-7765
Luciano C GreigDepartment of Stem Cell and Regenerative Biology, and Center for Brain Science, Harvard University, Cambridge, MA, USA.ORCID 0000-0002-0020-9379
Andrea J RomanowskiUniversity of Maryland School of Medicine, Department of Pharmacology, Baltimore, MD, USA.ORCID 0000-0001-8920-7400
Bogdan BudnikHarvard Center for Mass Spectrometry, Harvard University, Cambridge, MA, USA.ORCID 0000-0003-3622-2003
Jeffrey D MacklisDepartment of Stem Cell and Regenerative Biology, and Center for Brain Science, Harvard University, Cambridge, MA, USA.ORCID 0000-0003-3662-9698
Harvard University · USUniversity of Maryland, Baltimore · US

Funding

Training Grant in Cancer BiologyT32CA154274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Toni M Antalis, CURT I CIVIN · 2011 to 2026
$6.8M
Subcellular RNA-Proteome Mapping in Subtype- and Circuit-Specific Growth Cones: Development, Cell Biology, Disease, and RegenerationDP1NS106665 · NINDS · HARVARD UNIVERSITY · PI MACKLIS, JEFFREY D · 2017 to 2021
$5.9M
Multidisciplinary Schizophrenia Research TrainingT32MH067533 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI CARPENTER, WILLIAM T., ELMER, GREGORY I · 2004 to 2025
$4.3M
Untangling the biology of brain wiring: high-throughput innovations for molecular screening and functional targeting of circuit development in vivoDP2MH122398 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI POULOPOULOS, ALEXANDROS · 2019 to 2019
$2.3M
Molecular Development and Diversity of Callosal Projection NeuronsR01NS104055 · NINDS · HARVARD UNIVERSITY · PI MACKLIS, JEFFREY D · 2020 to 2024
$1.9M
A Lightsheet Microscope for an Established Core FacilityS10OD030221 · OD · UNIVERSITY OF MARYLAND BALTIMORE · PI BLANPIED, THOMAS A · 2021 to 2021
$600k
Novel BEAM and R26-BEACON recombinase-based systems for mosaic analysis of gene functionR21NS104733 · NINDS · HARVARD UNIVERSITY · PI MACKLIS, JEFFREY D · 2018 to 2019
$465k
Ctip1 Function in Neocortical Projection Neuron Subtype Specification and ArealizF31NS080343 · NINDS · HARVARD MEDICAL SCHOOL · PI CUSTO GREIG, LUCIANO F · 2012 to 2013
$72k
NCI NIH HHS T32 CA154274NIH HHS S10 OD030221NIMH NIH HHS DP2 MH122398NIMH NIH HHS T32 MH067533NINDS NIH HHS DP1 NS106665NINDS NIH HHS F31 NS080343NINDS NIH HHS R01 NS104055NINDS NIH HHS R21 NS104733
6 · The paper itself

Abstract

Specific and highly diverse connectivity between functionally specialized regions of the nervous system is controlled at multiple scales, from anatomically organized connectivity following macroscopic axon tracts to individual axon target-finding and synapse formation. Identifying mechanisms that enable entire subpopulations of related neurons to project their axons with regional specificity within stereotyped tracts to form appropriate long-range connectivity is key to understanding brain development, organization, and function. Here, we investigate how axons of the cerebral cortex form precise connections between the two cortical hemispheres via the corpus callosum. We identify topographic principles of the developing trans-hemispheric callosal tract that emerge through intrinsic guidance executed by growing axons in the corpus callosum within the first postnatal week in mice. Using micro-transplantation of regionally distinct neurons, subtype-specific growth cone purification, subcellular proteomics, and in utero gene manipulation, we investigate guidance mechanisms of transhemispheric axons. We find that adhesion molecule levels instruct tract topography and target field guidance. We propose a model in which transcallosal axons in the developing brain perform a "handshake" that is guided through co-fasciculation with symmetric contralateral axons, resulting in the stereotyped homotopic connectivity between the brain's hemispheres.

Identifiers

PMID38585721
PMCPMC10996634
OpenAlexW4393352866

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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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.