Evidence map›Paper›PMID 25874621›Full record

ArticlePloS one2015

A critical period for postnatal adaptive plasticity in a model of motor axon miswiring.

Michaela S Helmbrecht, Heidi Soellner, Maria A Castiblanco-Urbina, Stefan Winzeck, Julia Sundermeier, Fabian J Theis, Karim Fouad, Andrea B Huber

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Michaela S HelmbrechtInstitute of Developmental Genetics, Helmholtz-Zentrum München-German Research Center for Environmental Health (GmbH), Ingolstaedter Landstrasse 1, Neuherberg, Germany.
Heidi SoellnerInstitute of Developmental Genetics, Helmholtz-Zentrum München-German Research Center for Environmental Health (GmbH), Ingolstaedter Landstrasse 1, Neuherberg, Germany.
Maria A Castiblanco-UrbinaInstitute of Developmental Genetics, Helmholtz-Zentrum München-German Research Center for Environmental Health (GmbH), Ingolstaedter Landstrasse 1, Neuherberg, Germany.
Stefan WinzeckInstitute of Developmental Genetics, Helmholtz-Zentrum München-German Research Center for Environmental Health (GmbH), Ingolstaedter Landstrasse 1, Neuherberg, Germany.
Julia SundermeierInstitute of Developmental Genetics, Helmholtz-Zentrum München-German Research Center for Environmental Health (GmbH), Ingolstaedter Landstrasse 1, Neuherberg, Germany.
Fabian J TheisInstitute for Computational Biology, Helmholtz-Zentrum München-German Research Center for Environmental Health (GmbH), Ingolstaedter Landstrasse 1, Neuherberg, Germany; Department of Mathematics, Technische Universität München, Garching, Germany.
Karim FouadFaculty of Rehabilitation Medicine, University of Alberta, Edmonton, Canada.
Andrea B HuberInstitute of Developmental Genetics, Helmholtz-Zentrum München-German Research Center for Environmental Health (GmbH), Ingolstaedter Landstrasse 1, Neuherberg, Germany.
Helmholtz Zentrum München · DETechnical University of Munich · DEUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The correct wiring of neuronal circuits is of crucial importance for precise neuromuscular functionality. Therefore, guidance cues provide tight spatiotemporal control of axon growth and guidance. Mice lacking the guidance cue Semaphorin 3F (Sema3F) display very specific axon wiring deficits of motor neurons in the medial aspect of the lateral motor column (LMCm). While these deficits have been investigated extensively during embryonic development, it remained unclear how Sema3F mutant mice cope with these errors postnatally. We therefore investigated whether these animals provide a suitable model for the exploration of adaptive plasticity in a system of miswired neuronal circuitry. We show that the embryonically developed wiring deficits in Sema3F mutants persist until adulthood. As a consequence, these mutants display impairments in motor coordination that improve during normal postnatal development, but never reach wildtype levels. These improvements in motor coordination were boosted to wildtype levels by housing the animals in an enriched environment starting at birth. In contrast, a delayed start of enriched environment housing, at 4 weeks after birth, did not similarly affect motor performance of Sema3F mutants. These results, which are corroborated by neuroanatomical analyses, suggest a critical period for adaptive plasticity in neuromuscular circuitry. Interestingly, the formation of perineuronal nets, which are known to close the critical period for plastic changes in other systems, was not altered between the different housing groups. However, we found significant changes in the number of excitatory synapses on limb innervating motor neurons. Thus, we propose that during the early postnatal phase, when perineuronal nets have not yet been formed around spinal motor neurons, housing in enriched environment conditions induces adaptive plasticity in the motor system by the formation of additional synaptic contacts, in order to compensate for coordination deficits.

Indexed as

AnimalsAxonsBehavior, AnimalCholera ToxinElectromyographyGaitMaleMembrane ProteinsMiceMice, Inbred C57BLMotor NeuronsMotor SkillsMutationNerve Tissue ProteinsNeuronal PlasticitySpinal CordCholera ToxinMembrane ProteinsNerve Tissue ProteinsSema3f protein, mouse

Identifiers

PMID25874621
PMCPMC4395312
OpenAlexW2084260649

What OpenQuestion holds

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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.