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Role of microglia in development of epilepsy and behavioural comorbidities after a traumatic brain injury

Description 
Description Brain inflammation appears to play a critical role in the pathogenesis of epilepsy. A major cell type involved in inflammatory cascades are the microglial cells – brain-resident immune cells that become activated after epileptogenic brain injuries. Despite years of research in this area, a clear role of microglia in epilepsy development has not been established. This is partly due to the dynamic nature in which these cells get activated. The function of these cells can oscillate between different phenotypes that are associated with the release of either pro- or anti-inflammatory mediators. Therefore, depending on the stage after initial epileptogenic traumatic brain injury, their activation may promote brain repair processes or conversely accelerate the epilepsy development. This project will utilise animal models to identify the role of microglia at different stages of epilepsy development. This will be achieved by pharmacologically eliminating microglia at different timepoints following brain injury, and evaluate the relevant epilepsy outcomes by electrophysiological, molecular, immunofluorescence and imaging techniques.
Essential criteria: 
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords 
Traumatic brain injury, epilepsy, microglia, neuroinflammation
School 
School of Translational Medicine » Neuroscience
Available options 
PhD/Doctorate
Masters by coursework
Honours
BMedSc(Hons)
Time commitment 
Full-time
Top-up scholarship funding available 
No
Physical location 
Alfred Centre
Co-supervisors 
Assoc Prof 
Nigel C. Jones
Bridgette Semple

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