Evidence map›Paper›PMID 24152553›Full record

ArticleCell transplantation2015

Permissive Schwann cell graft/spinal cord interfaces for axon regeneration.

Ryan R Williams, Martha Henao, Damien D Pearse, Mary Bartlett Bunge

Open access · greenAbstract read
In one paragraph

Article in Cell transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
2.4field-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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Brain Plasticity in Patients with Spinal Cord Injuries: A Systematic Review.International journal of molecular sciences · 2024
    Pooled it
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  11. Cell transplantation to repair the injured spinal cord.International review of neurobiology · 2022
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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

4 authors at 2 institutions in 1 country.

Ryan R WilliamsThe Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, FL, USA.
Martha Henao
Damien D Pearse
Mary Bartlett Bunge
University of Miami · USNeurological Surgery · US

Funding

Stem cell therapy for spinal cord injuryP01NS038665 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI DIETRICH, W. DALTON DALTON · 2000 to 2004
$6.8M
CYTOLOGICAL STUDIES OF DEVELOPING &MATURE NEURONSR01NS009923 · NINDS · WASHINGTON UNIVERSITY · PI BETHEA, JOHN ROLAND, BUNGE, MARY BARTLETT · 1985 to 2016
$5.1M
Axon Regenration: Synergistic Actions of the MAPK and Cyclic AMP PathwaysR01NS056281 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PEARSE, DAMIEN D. · 2007 to 2010
$1.3M
NINDS NIH HHS P01 NS038665NINDS NIH HHS R01 NS009923NINDS NIH HHS R01 NS056281PHS HHS 09923Wellcome Trust 056281
6 · The paper itself

Abstract

The transplantation of autologous Schwann cells (SCs) to repair the injured spinal cord is currently being evaluated in a clinical trial. In support, this study determined properties of spinal cord/SC bridge interfaces that enabled regenerated brainstem axons to cross them, possibly leading to improvement in rat hindlimb movement. Fluid bridges of SCs and Matrigel were placed in complete spinal cord transections. Compared to pregelled bridges of SCs and Matrigel, they improved regeneration of brainstem axons across the rostral interface. The regenerating brainstem axons formed synaptophysin(+) bouton-like terminals and contacted MAP2A(+) dendrites at the caudal interface. Brainstem axon regeneration was directly associated with glial fibrillary acidic protein (GFAP(+)) astrocyte processes that elongated into the SC bridge. Electron microscopy revealed that axons, SCs, and astrocytes were enclosed together within tunnels bounded by a continuous basal lamina. Neuroglycan (NG2) expression was associated with these tunnels. One week after injury, the GFAP(+) processes coexpressed nestin and brain lipid-binding protein, and the tips of GFAP(+)/NG2(+) processes extended into the bridges together with the regenerating brainstem axons. Both brainstem axon regeneration and number of GFAP(+) processes in the bridges correlated with improvement in hindlimb locomotion. Following SCI, astrocytes may enter a reactive state that prohibits axon regeneration. Elongation of astrocyte processes into SC bridges, however, and formation of NG2(+) tunnels enable brainstem axon regeneration and improvement in function. It is important for spinal cord repair to define conditions that favor elongation of astrocytes into lesions/transplants.

Indexed as

Spinal Cord InjuriesSpinal Cord RegenerationAnimalsAntigensAstrocytesAutograftsAxonsChondroitin Sulfate Proteoglycan 4FemaleProteoglycansRatsRats, Inbred F344Schwann CellsAntigensChondroitin Sulfate Proteoglycan 4Proteoglycans

Identifiers

PMID24152553
PMCPMC4809058
OpenAlexW2327191065

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.