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Updated: Feb 2, 2026

A Pediatric Concussion Model in Mice: Closed Head Injury with Long-Term Disorders (CHILD)
Published on: February 7, 2025
Repeated Pediatric Concussions Evoke Long-Term Oligodendrocyte and White Matter Microstructural Dysregulation Distant
Jeong Bin Lee1, Bethann M Affeldt1, Yaritxa Gamboa1
1Department of Basic Sciences, Loma Linda University School of Medicine, Loma Linda, California, USA.
Insights
Mild traumatic brain injuries (mTBIs) in developing mice cause long-term white matter and behavioral issues. Repeated injuries lead to distinct white matter changes and oligodendrocyte dysfunction in the pediatric brain.
Area of Science:
- Neuroscience
- Developmental Biology
- Pathology
Background:
- Concussions (mild traumatic brain injuries) can cause lasting behavioral and cognitive problems.
- These deficits may worsen after repeated injuries, particularly in children involved in sports or falls.
- The impact of single or repeated mTBIs on developing white matter in children remains understudied.
Purpose of the Study:
- To investigate the long-term effects of single (s)mTBI and repeated (rmTBI) mild traumatic brain injuries on white matter (WM) structure and development in the pediatric brain.
- To examine the anterior commissure (AC), a WM tract distant from the injury site.
- To assess the impact on oligodendrocyte (OL) development and microstructural integrity.
Main Methods:
- Utilized a closed head injury (CHI) model in postnatal day 14 mice, employing bilateral repeated injuries.
- Applied diffusion tensor imaging (DTI) to assess WM microstructural integrity.
- Conducted immunohistochemistry (IHC) to evaluate oligodendrocyte development and myelin-related changes.
Main Results:
- Both s mTBI and rmTBI induced distinct myelin-related diffusion changes in WM.
- Abnormal oligodendrocyte development was observed in the anterior commissure (AC) following both injury types.
- Behavioral deficits were evident two months post-injury, suggesting long-term consequences.
Conclusions:
- Mild traumatic brain injuries cause long-term behavioral changes and white matter dysregulation linked to oligodendrocyte dysfunction in the developing brain.
- These findings highlight the importance of studying WM and OL development in pediatric TBI.
- Oligodendrocytes and WM development represent potential therapeutic targets for pediatric TBI.
Abstract:
Concussion or mild traumatic brain injury (mTBI) is often accompanied by long-term behavioral and neuropsychological deficits. Emerging data suggest that these deficits can be exacerbated following repeated injuries. However, despite the overwhelming prevalence of mTBI in children due to falls and sports-related activities, the effects of mTBI on white matter (WM) structure and its development in children have not been extensively examined. Moreover, the effect of repeated mTBI (rmTBI) on developing WM has not yet been studied, despite the possibility of exacerbated outcomes with repeat injuries. To address this knowledge gap, we investigated the long-term effects of single (s)mTBI and rmTBI on the WM in the pediatric brain, focusing on the anterior commissure (AC), a WM structure distant to the injury site, using diffusion tensor imaging (DTI) and immunohistochemistry (IHC). We hypothesized that smTBI and rmTBI to the developing mouse brain would lead to abnormalities in microstructural integrity and impaired oligodendrocyte (OL) development. We used a postnatal day 14 Ascl1-CreER: ccGFP mouse closed head injury (CHI) model with a bilateral repeated injury. We demonstrate that smTBI and rmTBI differentially lead to myelin-related diffusion changes in the WM and to abnormal OL development in the AC, which are accompanied by behavioral deficits 2 months after the initial injury. Our results suggest that mTBIs elicit long-term behavioral alterations and OL-associated WM dysregulation in the developing brain. These findings warrant additional research into the development of WM and OL as key components of pediatric TBI pathology and potential therapeutic targets.
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