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Updated: Jun 16, 2026

Long-Term Mouse Spinal Cord Organotypic Slice Culture as a Platform for Validating Cell Transplantation in Spinal Cord Injury
Published on: April 12, 2024
A systematic review of cellular transplantation therapies for spinal cord injury
Wolfram Tetzlaff1, Elena B Okon, Soheila Karimi-Abdolrezaee
1University of British Columbia, ICORD, Vancouver, British Columbia, Canada. tetzlaff@icord.org
Abstract:
Cell transplantation therapies have become a major focus in pre-clinical research as a promising strategy for the treatment of spinal cord injury (SCI). In this article, we systematically review the available pre-clinical literature on the most commonly used cell types in order to assess the body of evidence that may support their translation to human SCI patients. These cell types include Schwann cells, olfactory ensheathing glial cells, embryonic and adult neural stem/progenitor cells, fate-restricted neural/glial precursor cells, and bone-marrow stromal cells. Studies were included for review only if they described the transplantation of the cell substrate into an in-vivo model of traumatic SCI, induced either bluntly or sharply. Using these inclusion criteria, 162 studies were identified and reviewed in detail, emphasizing their behavioral effects (although not limiting the scope of the discussion to behavioral effects alone). Significant differences between cells of the same "type" exist based on the species and age of donor, as well as culture conditions and mode of delivery. Many of these studies used cell transplantations in combination with other strategies. The systematic review makes it very apparent that cells derived from rodent sources have been the most extensively studied, while only 19 studies reported the transplantation of human cells, nine of which utilized bone-marrow stromal cells. Similarly, the vast majority of studies have been conducted in rodent models of injury, and few studies have investigated cell transplantation in larger mammals or primates. With respect to the timing of intervention, nearly all of the studies reviewed were conducted with transplantations occurring subacutely and acutely, while chronic treatments were rare and often failed to yield functional benefits.
Insights
This review of cell transplantation for spinal cord injury (SCI) found that rodent cells and models dominate research. Human cell studies are limited, and chronic intervention timing often yields poor functional benefits.
Area of Science:
- Neuroscience
- Regenerative Medicine
- Cell Biology
Background:
- Cell transplantation is a key pre-clinical strategy for spinal cord injury (SCI) treatment.
- Numerous cell types are being investigated for their therapeutic potential in SCI.
- Translational success requires a thorough understanding of pre-clinical evidence.
Purpose of the Study:
- To systematically review pre-clinical literature on cell transplantation for SCI.
- To assess the evidence supporting the translation of various cell types to human SCI patients.
- To identify research gaps and trends in cell-based SCI therapies.
Main Methods:
- Systematic review of 162 in-vivo studies involving cell transplantation into traumatic SCI models.
- Inclusion criteria focused on traumatic SCI models and cell transplantation.
- Emphasis on behavioral effects, but scope included other outcomes.
Main Results:
- Rodent-derived cells and rodent SCI models are most extensively studied.
- Only 19 studies used human cells, primarily bone-marrow stromal cells.
- Most studies used acute or subacute transplantation; chronic interventions were rare and often ineffective.
- Significant variability exists within cell types based on donor species, age, culture, and delivery.
Conclusions:
- The current pre-clinical evidence for cell transplantation in SCI is heavily biased towards rodent models and cells.
- Further research is needed using human cells and larger animal models to facilitate clinical translation.
- Optimizing the timing of cell delivery, particularly exploring chronic interventions, is crucial for improving functional recovery in SCI.
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