Evidence map›Paper›PMID 26053681›Full record

ArticleScientific reports2015

Human Embryonic Stem Cell-Derived Progenitors Assist Functional Sensory Axon Regeneration after Dorsal Root Avulsion Injury.

Jan Hoeber, Carl Trolle, Niclas Konig, Zhongwei Du, Alessandro Gallo, Emmanuel Hermans, Hakan Aldskogius, Peter Shortland, Su-Chun Zhang, Ronald Deumens and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Sensory regeneration in dorsal root avulsion.Neural regeneration research · 2015
    Article
  9. Article
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

11 authors.

Jan HoeberUppsala University, Department of Neuroscience, Husargatan 3, 75124 Uppsala, Sweden.
Carl TrolleUppsala University, Department of Neuroscience, Husargatan 3, 75124 Uppsala, Sweden.
Niclas KonigUppsala University, Department of Neuroscience, Husargatan 3, 75124 Uppsala, Sweden.
Zhongwei DuWaisman Center, University of Wisconsin, 1500 Highland Avenue, Madison, WI 53705, USA.
Alessandro GalloInstitute of Neuroscience, Université Catholique de Louvain, Avenue Hippocrate 54, 1200, Brussels, Belgium.
Emmanuel HermansInstitute of Neuroscience, Université Catholique de Louvain, Avenue Hippocrate 54, 1200, Brussels, Belgium.
Hakan AldskogiusUppsala University, Department of Neuroscience, Husargatan 3, 75124 Uppsala, Sweden.
Peter ShortlandMedical Sciences, School of Science and Health, University of Western Sydney, Campbelltown Campus, Narellan Road, NSW 2567, Australia.
Su-Chun ZhangWaisman Center, University of Wisconsin, 1500 Highland Avenue, Madison, WI 53705, USA.
Ronald DeumensInstitute of Neuroscience, Université Catholique de Louvain, Avenue Hippocrate 54, 1200, Brussels, Belgium.
Elena N KozlovaUppsala University, Department of Neuroscience, Husargatan 3, 75124 Uppsala, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dorsal root avulsion results in permanent impairment of sensory functions due to disconnection between the peripheral and central nervous system. Improved strategies are therefore needed to reconnect injured sensory neurons with their spinal cord targets in order to achieve functional repair after brachial and lumbosacral plexus avulsion injuries. Here, we show that sensory functions can be restored in the adult mouse if avulsed sensory fibers are bridged with the spinal cord by human neural progenitor (hNP) transplants. Responses to peripheral mechanical sensory stimulation were significantly improved in transplanted animals. Transganglionic tracing showed host sensory axons only in the spinal cord dorsal horn of treated animals. Immunohistochemical analysis confirmed that sensory fibers had grown through the bridge and showed robust survival and differentiation of the transplants. Section of the repaired dorsal roots distal to the transplant completely abolished the behavioral improvement. This demonstrates that hNP transplants promote recovery of sensorimotor functions after dorsal root avulsion, and that these effects are mediated by spinal ingrowth of host sensory axons. These results provide a rationale for the development of novel stem cell-based strategies for functionally useful bridging of the peripheral and central nervous system.

Indexed as

AnimalsAxonsGanglia, SpinalHuman Embryonic Stem CellsHumansMaleMiceNerve RegenerationSensory Receptor CellsSpinal CordSpinal Cord InjuriesSpinal Nerve RootsStem Cells

Identifiers

PMID26053681
PMCPMC4459081

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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.