Evidence map›Paper›PMID 32112058›Full record

ArticleNature neuroscience2020

Microglia and macrophages promote corralling, wound compaction and recovery after spinal cord injury via Plexin-B2.

Xiang Zhou, Shalaka Wahane, Marie-Sophie Friedl, Michael Kluge, Caroline C Friedel, Kleopatra Avrampou, Venetia Zachariou, Lei Guo, Bin Zhang, Xijing He and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 164 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
164citing papers in PubMed, 2 pooled it
16.2field-weighted citation impact, top 1% 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

164 citing papers in PubMed, 2 syntheses or guidelines pooled it, 275 citations in OpenAlex.

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104 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 3 countries.

Xiang Zhou *Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Shalaka Wahane *Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-3795-6407
Marie-Sophie FriedlInstitut für Informatik, Ludwig-Maximilians-Universität München, Munich, Germany.
Michael KlugeInstitut für Informatik, Ludwig-Maximilians-Universität München, Munich, Germany.
Caroline C FriedelInstitut für Informatik, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID http://orcid.org/0000-0003-3569-4877
Kleopatra AvrampouNash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Venetia ZachariouNash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Lei GuoDepartment of Genetics and Genomic Sciences, Mount Sinai Center for Transformative Disease Modeling, Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Bin ZhangDepartment of Genetics and Genomic Sciences, Mount Sinai Center for Transformative Disease Modeling, Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Xijing HeDepartment of Orthopedics, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Roland H FriedelNash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. roland.friedel@mssm.edu.ORCID http://orcid.org/0000-0002-7513-3604
Hongyan ZouNash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. hongyan.zou@mssm.edu.ORCID http://orcid.org/0000-0003-4216-5607
Allen Institute for Brain Science · USLudwig-Maximilians-Universität München · DEIcahn School of Medicine at Mount Sinai · USXi’an International University · CN

Funding

Integrative Network Biology Approaches to Identify, Characterize and Validate Molecular Subtypes in Alzheimer's DiseaseU01AG046170 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI EHRLICH, MICHELLE E, GANDY, SAMUEL E. · 2013 to 2022
$26.0M
Transcription Factors in Stimulant and Opioid ActionP01DA047233 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Anne Schaefer · 2019 to 2026
$16.5M
Cellular Mechanisms of Antidepressant Drug Actions in Neuropathic Pain ModelsR01NS086444 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZACHARIOU, VENETIA · 2014 to 2023
$4.4M
Plexin-B2 function in glioma invasion and glioma stem cell maintenanceR01NS092735 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIEDEL, ROLAND HORST · 2016 to 2025
$4.1M
Towards a comprehensive signaling pathway map of parahippocampal vulnerability in Alzheimers DiseaseRF1AG057440 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAROUTUNIAN, VAHRAM, NOGGLE, SCOTT ALLEN · 2017 to 2017
$3.5M
A Female Specific Role of RGSz1 in Modulation of Chronic PainR01NS111351 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZACHARIOU, VENETIA · 2020 to 2024
$1.9M
Promoting axon regeneration by activation of the Smad1 signaling pathwayR01NS073596 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZOU, HONGYAN JENNY · 2011 to 2015
$1.7M
Leica TCS SP8 STED3XS10OD021838 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BENSON, DEANNA L · 2017 to 2017
$1.2M
HDAC5 in the nucleus accumbens modulates the actions of antidepressant drugs in models of neuropathic painR21NS093537 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZACHARIOU, VENETIA · 2015 to 2016
$461k
Promoting Axon regeneration in Spinal Cord Injury by Epigenetic ModulationR56NS073596 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZOU, HONGYAN JENNY · 2017 to 2017
$431k
NIA NIH HHS RF1 AG057440NIA NIH HHS U01 AG046170NIDA NIH HHS P01 DA047233NIH HHS S10 OD021838NINDS NIH HHS R01 NS073596NINDS NIH HHS R01 NS086444NINDS NIH HHS R01 NS092735NINDS NIH HHS R01 NS111351NINDS NIH HHS R21 NS093537NINDS NIH HHS R56 NS073596
6 · The paper itself

Abstract

Tissue repair after spinal cord injury requires the mobilization of immune and glial cells to form a protective barrier that seals the wound and facilitates debris clearing, inflammatory containment and matrix compaction. This process involves corralling, wherein phagocytic immune cells become confined to the necrotic core, which is surrounded by an astrocytic border. Here we elucidate a temporally distinct gene signature in injury-activated microglia and macrophages (IAMs) that engages axon guidance pathways. Plexin-B2 is upregulated in IAMs and is required for motor sensory recovery after spinal cord injury. Plexin-B2 deletion in myeloid cells impairs corralling, leading to diffuse tissue damage, inflammatory spillover and hampered axon regeneration. Corralling begins early and requires Plexin-B2 in both microglia and macrophages. Mechanistically, Plexin-B2 promotes microglia motility, steers IAMs away from colliding cells and facilitates matrix compaction. Our data therefore establish Plexin-B2 as an important link that integrates biochemical cues and physical interactions of IAMs with the injury microenvironment during wound healing.

Indexed as

AnimalsAxonsCellular MicroenvironmentLocomotionMacrophagesMiceMicrogliaNerve RegenerationNerve Tissue ProteinsNeural PathwaysPhagocytosisRecovery of FunctionSensationSpinal Cord InjuriesWound HealingNerve Tissue ProteinsPlxnb2 protein, mouse

Identifiers

PMID32112058
PMCPMC7412870
OpenAlexW3008198525

What OpenQuestion holds

Textmetadata
LicenceTDM
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.