Evidence map›Paper›PMID 27191729›Full record

ArticleExperimental neurology2016

Lumbar Myeloid Cell Trafficking into Locomotor Networks after Thoracic Spinal Cord Injury.

Christopher N Hansen, Diana M Norden, Timothy D Faw, Rochelle Deibert, Eric S Wohleb, John F Sheridan, Jonathan P Godbout, D Michele Basso

Abstract read
In one paragraph

Article in Experimental neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Matrix metalloproteinase signals following neurotrauma are right on cue.Cellular and molecular life sciences : CMLS · 2019
    Review
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  8. Article
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  12. Review
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 2 institutions in 1 country.

Christopher N HansenCenter for Brain and Spinal Cord Repair, The Ohio State University, Columbus, OH 43210, USA; School of Health and Rehabilitation Sciences, The Ohio State University, Columbus, OH 43210, USA; Department of Neuroscience, The Ohio State University, Columbus, OH 43210, USA.
Diana M NordenCenter for Brain and Spinal Cord Repair, The Ohio State University, Columbus, OH 43210, USA; School of Health and Rehabilitation Sciences, The Ohio State University, Columbus, OH 43210, USA; Department of Neuroscience, The Ohio State University, Columbus, OH 43210, USA.
Timothy D FawCenter for Brain and Spinal Cord Repair, The Ohio State University, Columbus, OH 43210, USA; School of Health and Rehabilitation Sciences, The Ohio State University, Columbus, OH 43210, USA; Department of Neuroscience, The Ohio State University, Columbus, OH 43210, USA; Neuroscience Graduate Program, The Ohio State University, Columbus, OH 43210, USA.
Rochelle DeibertCenter for Brain and Spinal Cord Repair, The Ohio State University, Columbus, OH 43210, USA; School of Health and Rehabilitation Sciences, The Ohio State University, Columbus, OH 43210, USA.
Eric S WohlebDepartment of Neuroscience, The Ohio State University, Columbus, OH 43210, USA; Division of Biosciences, , The Ohio State University, Columbus, OH 43210, USA. Electronic address: eric.wohleb@yale.edu.
John F SheridanCenter for Brain and Spinal Cord Repair, The Ohio State University, Columbus, OH 43210, USA; Division of Biosciences, , The Ohio State University, Columbus, OH 43210, USA; Institute for Behavioral Medicine Research, The Ohio State University, Columbus, OH 43210, USA.
Jonathan P GodboutCenter for Brain and Spinal Cord Repair, The Ohio State University, Columbus, OH 43210, USA; Department of Neuroscience, The Ohio State University, Columbus, OH 43210, USA; Institute for Behavioral Medicine Research, The Ohio State University, Columbus, OH 43210, USA.
D Michele BassoCenter for Brain and Spinal Cord Repair, The Ohio State University, Columbus, OH 43210, USA; School of Health and Rehabilitation Sciences, The Ohio State University, Columbus, OH 43210, USA. Electronic address: Michele.Basso@osumc.edu.
The Ohio State University · USInstitute for Behavioral Medicine · US

Funding

Behavioral and Cellular Determinants of Treadmill Training and Recovery After SCIR01NS074882 · NINDS · OHIO STATE UNIVERSITY · PI BASSO, D M · 2011 to 2020
$3.3M
Peripheral Trafficking in Locomotor Networks After Thoracic SCIR21NS090265 · NINDS · OHIO STATE UNIVERSITY · PI BASSO, D M · 2014 to 2015
$424k
Characterization of lumbar plasticity and remote injury mechanisms after SCIF31NS080512 · NINDS · OHIO STATE UNIVERSITY · PI HANSEN, CHRISTOPHER N. · 2012 to 2013
$62k
NINDS NIH HHS F31 NS080512NINDS NIH HHS R01 NS074882NINDS NIH HHS R21 NS090265
6 · The paper itself

Abstract

Spinal cord injury (SCI) promotes inflammation along the neuroaxis that jeopardizes plasticity, intrinsic repair and recovery. While inflammation at the injury site is well-established, less is known within remote spinal networks. The presence of bone marrow-derived immune (myeloid) cells in these areas may further impede functional recovery. Previously, high levels of the gelatinase, matrix metalloproteinase-9 (MMP-9) occurred within the lumbar enlargement after thoracic SCI and impeded activity-dependent recovery. Since SCI-induced MMP-9 potentially increases vascular permeability, myeloid cell infiltration may drive inflammatory toxicity in locomotor networks. Therefore, we examined neurovascular reactivity and myeloid cell infiltration in the lumbar cord after thoracic SCI. We show evidence of region-specific recruitment of myeloid cells into the lumbar but not cervical region. Myeloid infiltration occurred with concomitant increases in chemoattractants (CCL2) and cell adhesion molecules (ICAM-1) around lumbar vasculature 24h and 7days post injury. Bone marrow GFP chimeric mice established robust infiltration of bone marrow-derived myeloid cells into the lumbar gray matter 24h after SCI. This cell infiltration occurred when the blood-spinal cord barrier was intact, suggesting active recruitment across the endothelium. Myeloid cells persisted as ramified macrophages at 7days post injury in parallel with increased inhibitory GAD67 labeling. Importantly, macrophage infiltration required MMP-9.

Indexed as

Analysis of VarianceAnimalsCapillary PermeabilityCD11b AntigenCell MovementCell TrackingChemokine CCL2Chemokine CXCL12Disease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryGlutamate DecarboxylaseGreen Fluorescent ProteinsIntercellular Adhesion Molecule-1LocomotionCD11b AntigenChemokine CCL2Chemokine CXCL12Glutamate Decarboxylaseglutamate decarboxylase 1Green Fluorescent ProteinsIntercellular Adhesion Molecule-1Matrix Metalloproteinase 9Blood brain barrierInflammationMacrophageMMP-9Spinal cord injury

Identifiers

PMID27191729
PMCPMC4930359
OpenAlexW2404533602

What OpenQuestion holds

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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.