Related Experiment Video
Updated: Feb 2, 2026

A Tissue Displacement-based Contusive Spinal Cord Injury Model in Mice
Published on: June 18, 2017
Olig2-expressing Mesenchymal Stem Cells Enhance Functional Recovery after Contusive Spinal Cord Injury
Hwan-Woo Park1,2, Soonyi Oh1, Kyung Hee Lee3
1Laboratory of Stem Cell & Neurobiology, Department of Oral Anatomy, Dental Research Institute & School of Dentistry, Seoul National University, Seoul, Korea.
Background And Objectives:
Glial scarring and inflammation after spinal cord injury (SCI) interfere with neural regeneration and functional recovery due to the inhibitory microenvironment of the injured spinal cord. Stem cell transplantation can improve functional recovery in experimental models of SCI, but many obstacles to clinical application remain due to concerns regarding the effectiveness and safety of stem cell transplantation for SCI patients. In this study, we investigated the effects of transplantation of human mesenchymal stem cells (hMSCs) that were genetically modified to express Olig2 in a rat model of SCI.
Methods:
Bone marrow-derived hMSCs were genetically modified to express Olig2 and transplanted one week after the induction of contusive SCI in a rat model. Spinal cords were harvested 7 weeks after transplantation.
Results:
Transplantation of Olig2-expressing hMSCs significantly improved functional recovery in a rat model of contusive SCI model compared to the control hMSC-transplanted group. Transplantation of Olig2-expressing hMSCs also attenuated glial scar formation in spinal cord lesions. Immunohistochemical analysis showed that transplanted Olig2-expressing hMSCs were partially differentiated into Olig1-positive oligodendrocyte-like cells in spinal cords. Furthermore, NF-M-positive axons were more abundant in the Olig2-expressing hMSC-transplanted group than in the control hMSC-transplanted group.
Conclusions:
We suggest that Olig2-expressing hMSCs are a safe and optimal cell source for treating SCI.
Insights
Transplanting genetically modified human mesenchymal stem cells (hMSCs) expressing Olig2 improved functional recovery and reduced glial scarring in a rat spinal cord injury (SCI) model. These Olig2-hMSCs show promise for SCI treatment.
Area of Science:
- Neuroscience
- Regenerative Medicine
- Cell Therapy
Background:
- Spinal cord injury (SCI) causes glial scarring and inflammation, inhibiting neural regeneration.
- Stem cell transplantation shows potential for SCI recovery but faces clinical application challenges.
- The inhibitory microenvironment post-SCI hinders functional recovery.
Purpose of the Study:
- To investigate the therapeutic potential of human mesenchymal stem cells (hMSCs) genetically modified to express Olig2 in a rat SCI model.
- To assess the effects of Olig2-hMSC transplantation on functional recovery and the spinal cord microenvironment.
Main Methods:
- Bone marrow-derived hMSCs were genetically modified to express Olig2.
- hMSCs (Olig2-modified or control) were transplanted one week after inducing contusive SCI in rats.
- Spinal cords were analyzed 7 weeks post-transplantation.
Main Results:
- Olig2-hMSC transplantation significantly improved functional recovery compared to control hMSCs.
- Transplantation of Olig2-hMSCs attenuated glial scar formation in spinal cord lesions.
- Olig2-hMSCs differentiated into oligodendrocyte-like cells, and axonal regeneration (NF-M positive) increased.
Conclusions:
- Olig2-expressing hMSCs represent a safe and effective cell source for SCI treatment.
- Olig2 modification enhances the therapeutic efficacy of hMSCs for spinal cord repair.
Related Concept Videos
Mesenchymal Stem Cells
Spinal Cord
The Spinal Cord
Spinal Cord: Information Processing
Sensory Information Processing
Sensory information processing begins at the sensory receptors located in the skin and other tissues, which detect somatic sensory stimuli such as touch, temperature, or pain. These receptors function as catalysts, initiating...
Spinal Cord: Gross Anatomy
Spinal Cord: Cross-sectional Anatomy
Gray Matter and its Components
Central to the gray matter is...

