Evidence map›Paper›PMID 41173548›Full record

ArticleStem cells translational medicine2025

Oligodendrogenic neural progenitors for treatment of chronic compressive cervical spinal cord injury.

Zixiang Luo, Zijian Lou, Mohammad-Masoud Zavvarian, Sogolie Kouhzaei, Jian Wang, James Hong, Seong Jun Kim, Jianzhong Hu, Mohamad Khazaei, Michael G Fehlings

Abstract read
In one paragraph

Article in Stem cells translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Zixiang LuoDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
Zijian LouDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
Mohammad-Masoud ZavvarianDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
Sogolie KouhzaeiDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
Jian WangDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
James HongDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
Seong Jun KimDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
Jianzhong HuDepartment of Spine Surgery and Orthopaedics, Xiangya Hospital, Central South University, Changsha 410008, Hunan, China.
Mohamad KhazaeiDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.
Michael G FehlingsDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON M5T 0S8, Canada.ORCID 0000-0002-5722-6364

Funding

Canada First Research Excellence Fund "Medicine by Design" Pivotal Experiment Fund
6 · The paper itself

Abstract

Chronic compressive cervical spinal cord injury (cCSCI), a debilitating condition, lacks effective treatment options. Addressing this gap, our study introduces a novel rat model of cCSCI developed through spinal cord compression via synthetic polyether sheet implantation, closely mimicking human pathology. We evaluated the model's fidelity utilizing a comprehensive series of behavioral, electrophysiological, and histological assessments. Our research also explored the therapeutic potential of oligodendrogenic neural progenitor cells (oNPCs) derived from induced pluripotent stem cells. Transplanted oNPCs successfully integrated into the host spinal cord, differentiated into neurons, astrocytes, and oligodendrocytes, and demonstrated a remarkable capacity for enhancing neuroplasticity. Electrophysiological analyses revealed significant improvements in motor evoked potentials and a rectification of the excitability imbalance posttransplantation, indicating substantial recovery of motor circuits. Histological findings complemented these results, showing enhanced remyelination and a reduction in excitatory transmitter expression in the residual gray matter. Functionally, the transplantation of oNPCs led to marked improvements in grip strength, locomotor abilities, and sensory functions, surpassing those seen with standard treatments. This study not only provides a novel and reliable rat model of cCSCI for further research but also highlights the potential of oNPCs as a transformative approach for spinal cord injury therapy, suggesting their significant role in neural regeneration and repair.

Indexed as

Neural Stem CellsOligodendrogliaSpinal Cord CompressionSpinal Cord InjuriesAnimalsCell DifferentiationCervical CordDisease Models, AnimalFemaleInduced Pluripotent Stem CellsRatsRats, Sprague-Dawleycell transplantationchronic cervical spinal cord injuryneuroplasticity repairoligodendrogenic neural progenitor cells

Identifiers

PMID41173548
PMCPMC12578511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.