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Updated: Jun 30, 2026

Advanced Diffusion Imaging in The Hippocampus of Rats with Mild Traumatic Brain Injury
Published on: August 14, 2019
Cellular infiltration in traumatic brain injury
Aftab Alam1, Eric P Thelin2,3,4, Tamara Tajsic2
1Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK. alam.camb@gmail.com.
Abstract:
Traumatic brain injury leads to cellular damage which in turn results in the rapid release of damage-associated molecular patterns (DAMPs) that prompt resident cells to release cytokines and chemokines. These in turn rapidly recruit neutrophils, which assist in limiting the spread of injury and removing cellular debris. Microglia continuously survey the CNS (central nervous system) compartment and identify structural abnormalities in neurons contributing to the response. After some days, when neutrophil numbers start to decline, activated microglia and astrocytes assemble at the injury site-segregating injured tissue from healthy tissue and facilitating restorative processes. Monocytes infiltrate the injury site to produce chemokines that recruit astrocytes which successively extend their processes towards monocytes during the recovery phase. In this fashion, monocytes infiltration serves to help repair the injured brain. Neurons and astrocytes also moderate brain inflammation via downregulation of cytotoxic inflammation. Depending on the severity of the brain injury, T and B cells can also be recruited to the brain pathology sites at later time points.
Insights
Traumatic brain injury triggers a cascade of cellular damage and immune responses, involving neutrophils, microglia, and astrocytes. These cells work to clear debris, contain injury, and initiate repair processes in the central nervous system.
Area of Science:
- Neuroscience
- Immunology
- Cell Biology
Background:
- Traumatic brain injury (TBI) causes cellular damage, releasing damage-associated molecular patterns (DAMPs).
- DAMPs initiate inflammatory responses involving cytokines and chemokines, recruiting immune cells to the injury site.
- Resident glial cells, including microglia and astrocytes, play crucial roles in the early and later stages of TBI response.
Purpose of the Study:
- To elucidate the sequential cellular and molecular events following traumatic brain injury.
- To understand the roles of various immune cells and glial cells in the brain's response to TBI.
- To identify mechanisms contributing to both injury progression and repair after TBI.
Main Methods:
- Observational study detailing cellular responses post-TBI.
- Analysis of immune cell infiltration and glial activation dynamics.
- Investigation of signaling pathways involving DAMPs, cytokines, and chemokines.
Main Results:
- Neutrophils are rapidly recruited to clear debris and limit injury spread.
- Microglia and astrocytes form a barrier at the injury site, facilitating repair.
- Monocyte infiltration aids in astrocyte recruitment and brain tissue repair.
- Neurons and astrocytes modulate inflammation, while T and B cells may be recruited later.
Conclusions:
- The brain mounts a complex, multi-stage immune and cellular response to traumatic brain injury.
- Specific immune cells and glial cells orchestrate distinct phases of injury management and repair.
- Understanding these cellular dynamics is crucial for developing therapeutic strategies for TBI.
Related Concept Videos
Cellular Injury I: Introduction
Cellular Injury II: Classification
Bacterial Meningitis II: Pathophysiology
Traumatic Brain Injury l: Introduction
Increased Intracranial Pressure ll: Pathophysiology
Cerebral Edema ll: Pathophysiology

