Mild and repetitive mild traumatic brain injury: Changes in microglial cells and synapses

Adna Smajkan1,2,3, Elizabeth Naranjo-Cinto1,2,4, Florence M Bareyre1,2,5

  • 1Institute of Clinical Neuroimmunology, University Hospital, LMU Munich, Munich, Germany.

PubMed

Insights

Repetitive mild traumatic brain injury (mTBI) causes cumulative deficits by altering synaptic function and activating immune cells. Understanding these microglial and synaptic changes is crucial for managing chronic neurodegenerative conditions.

Area of Science:

  • Neuroscience
  • Immunology
  • Traumatic Brain Injury Research

Background:

  • Mild traumatic brain injury (mTBI) stems from external head trauma.
  • Repetitive mTBI (rmTBI) is common in sports and abuse, increasing risks of neurodegeneration.
  • Recent research focuses on subtle synaptic and microglial changes post-mTBI.

Purpose of the Study:

  • To review current literature on mTBI and rmTBI.
  • To emphasize microglial and synaptic alterations following these injuries.

Main Methods:

  • Literature review of studies on mTBI and rmTBI.
  • Focus on synaptic function and microglial cell activation.
  • Analysis of morphological and functional changes.

Main Results:

  • Single mTBI causes transient synaptic alterations, including increased excitation and disrupted plasticity.
  • Microglial cells activate rapidly and persistently post-mTBI.
  • rmTBI leads to pronounced microglial priming, neuroimmune dysregulation, and heightened vulnerability.

Conclusions:

  • Synaptic and microglial changes are critical early events in mTBI.
  • rmTBI exacerbates neuroimmune dysregulation, increasing chronic risks.
  • Further research into these mechanisms is vital for therapeutic strategies.