Evidence map›Paper›PMID 33443682›Full record

ArticleMolecular neurobiology2021

Improvement of Rat Spinal Cord Injury Following Lentiviral Vector-Transduced Neural Stem/Progenitor Cells Derived from Human Epileptic Brain Tissue Transplantation with a Self-assembling Peptide Scaffold.

Sara Abdolahi, Hadi Aligholi, Azizollah Khodakaram-Tafti, Maryam Khaleghi Ghadiri, Walter Stummer, Ali Gorji

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 21% 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, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Research Progress on Biomaterials for Spinal Cord Repair.International journal of nanomedicine · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Spinal cord injury: molecular mechanisms and therapeutic interventions.Signal transduction and targeted therapy · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. 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

6 authors at 4 institutions in 2 countries.

Sara AbdolahiDepartment of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Hadi AligholiDepartment of Neuroscience, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.
Azizollah Khodakaram-TaftiDepartment of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Maryam Khaleghi GhadiriDepartment of Neurosurgery, Westfälische Wilhelms-Universität, Münster, Germany.
Walter StummerDepartment of Neurosurgery, Westfälische Wilhelms-Universität, Münster, Germany.
Ali GorjiShefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran. gorjial@uni-muenster.de.ORCID http://orcid.org/0000-0002-4557-3270
Shiraz University · IRUniversity of Münster · DEMashhad University of Medical Sciences · IRShiraz University of Medical Sciences · IR

Funding

National Institute for Medical Research Development 964650
6 · The paper itself

Abstract

Spinal cord injury (SCI) is a disabling neurological disorder that causes neural circuit dysfunction. Although various therapies have been applied to improve the neurological outcomes of SCI, little clinical progress has been achieved. Stem cell-based therapy aimed at restoring the lost cells and supporting micromilieu at the site of the injury has become a conceptually attractive option for tissue repair following SCI. Adult human neural stem/progenitor cells (hNS/PCs) were obtained from the epileptic human brain specimens. Induction of SCI was followed by the application of lentiviral vector-mediated green fluorescent protein-labeled hNS/PCs seeded in PuraMatrix peptide hydrogel (PM). The co-application of hNS/PCs and PM at the SCI injury site significantly enhanced cell survival and differentiation, reduced the lesion volume, and improved neurological functions compared to the control groups. Besides, the transplanted hNS/PCs seeded in PM revealed significantly higher migration abilities into the lesion site and the healthy host tissue as well as a greater differentiation into astrocytes and neurons in the vicinity of the lesion as well as in the host tissue. Our data suggest that the transplantation of hNS/PCs seeded in PM could be a promising approach to restore the damaged tissues and improve neurological functions after SCI.

Indexed as

Brain Tissue TransplantationTransduction, GeneticAnimalsBrainCell SurvivalDoublecortin Domain ProteinsEpilepsyGenetic VectorsGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsHumansLentivirusMaleMicrotubule-Associated ProteinsNeural Stem CellsNeuropeptidesDoublecortin Domain ProteinsGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsMicrotubule-Associated ProteinsNeuropeptidesPeptidesBioengineeringCell therapyDisabilityScaffoldTrauma

Identifiers

PMID33443682
PMCPMC8128971
OpenAlexW3119836765

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.