Evidence map›Paper›PMID 28559442›Full record

ArticleEMBO molecular medicine2017

CXCL12α/SDF-1 from perisynaptic Schwann cells promotes regeneration of injured motor axon terminals.

Samuele Negro, Francesca Lessi, Elisa Duregotti, Paolo Aretini, Marco La Ferla, Sara Franceschi, Michele Menicagli, Elisanna Bergamin, Egle Radice, Marcus Thelen and 5 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

44 citing papers in PubMed, 73 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

15 authors at 3 institutions in 2 countries.

Samuele NegroDepartment of Biomedical Sciences, University of Padua, Padua, Italy.
Francesca LessiLaboratory of Genomics, Pisa Science Foundation, Pisa, Italy.
Elisa DuregottiDepartment of Biomedical Sciences, University of Padua, Padua, Italy.
Paolo AretiniLaboratory of Genomics, Pisa Science Foundation, Pisa, Italy.
Marco La FerlaLaboratory of Genomics, Pisa Science Foundation, Pisa, Italy.
Sara FranceschiLaboratory of Genomics, Pisa Science Foundation, Pisa, Italy.
Michele MenicagliLaboratory of Genomics, Pisa Science Foundation, Pisa, Italy.
Elisanna BergaminDepartment of Biomedical Sciences, University of Padua, Padua, Italy.
Egle RadiceInstitute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona, Switzerland.
Marcus ThelenInstitute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona, Switzerland.
Aram MegighianDepartment of Biomedical Sciences, University of Padua, Padua, Italy.
Marco PirazziniDepartment of Biomedical Sciences, University of Padua, Padua, Italy.
Chiara M MazzantiLaboratory of Genomics, Pisa Science Foundation, Pisa, Italy c.mazzanti@fondazionepisascienza.org michela.rigoni@unipd.it cesare.montecucco@unipd.it.ORCID 0000-0002-7249-9221
Michela RigoniDepartment of Biomedical Sciences, University of Padua, Padua, Italy c.mazzanti@fondazionepisascienza.org michela.rigoni@unipd.it cesare.montecucco@unipd.it.ORCID 0000-0003-1763-2648
Cesare MontecuccoDepartment of Biomedical Sciences, University of Padua, Padua, Italy c.mazzanti@fondazionepisascienza.org michela.rigoni@unipd.it cesare.montecucco@unipd.it.ORCID 0000-0001-7361-5688
University of Padua · ITFondazione Pisa · ITUniversità della Svizzera italiana · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The neuromuscular junction has retained through evolution the capacity to regenerate after damage, but little is known on the inter-cellular signals involved in its functional recovery from trauma, autoimmune attacks, or neurotoxins. We report here that CXCL12α, also abbreviated as stromal-derived factor-1 (SDF-1), is produced specifically by perisynaptic Schwann cells following motor axon terminal degeneration induced by α-latrotoxin. CXCL12α acts via binding to the neuronal CXCR4 receptor. A CXCL12α-neutralizing antibody or a specific CXCR4 inhibitor strongly delays recovery from motor neuron degeneration

Indexed as

RegenerationAnimalsChemokine CXCL12Disease Models, AnimalMice, Inbred C57BLMotor NeuronsPresynaptic TerminalsReceptors, CXCR4Schwann CellsSnake BitesSpider Venomsalpha-latrotoxinChemokine CXCL12Cxcl12 protein, mouseCXCR4 protein, mouseReceptors, CXCR4Spider VenomsCXCL12CXCR4neuromuscular junctionneuroregenerationperisynaptic Schwann cells

Identifiers

PMID28559442
PMCPMC5538331
OpenAlexW2617691195

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.