Imperial College London
Portrait Picture

DrGregoryScott

Faculty of Medicine, Department of Brain Sciences

Post-CCT Research Fellow (IPPRF)
 
 
 
//

Contact

 

gregory.scott99

 
 
//

Location

 

C3NL, Burlington DanesBurlington DanesHammersmith Campus

//

Summary

 

Publications

Citation

BibTex format

@article{Donat:2017:10.3389/fnagi.2017.00208,
author = {Donat, CK and Scott, G and Gentleman, S and Sastre, M},
doi = {10.3389/fnagi.2017.00208},
journal = {Frontiers in Aging Neuroscience},
title = {Microglial activation in traumatic brain injury},
url = {http://dx.doi.org/10.3389/fnagi.2017.00208},
volume = {9},
year = {2017}
}
Download

RIS format (EndNote, RefMan)

TY  - JOUR
AB  - Microglia have a variety of functions in the brain, including synaptic pruning, CNS repair and mediating the immune response against peripheral infection. Microglia rapidly become activated in response to CNS damage. Depending on the nature of the stimulus, microglia can take a number of activation states, which correspond to altered microglia morphology, gene expression and function. It has been reported that early microglia activation following traumatic brain injury (TBI) may contribute to the restoration of homeostasis in the brain. On the other hand, if they remain chronically activated, such cells display a classically activated phenotype, releasing pro-inflammatory molecules, resulting in further tissue damage and contributing potentially to neurodegeneration. However, new evidence suggests that this classification is over-simplistic and the balance of activation states can vary at different points. In this article, we review the role of microglia in TBI, analyzing their distribution, morphology and functional phenotype over time in animal models and in humans. Animal studies have allowed genetic and pharmacological manipulations of microglia activation, in order to define their role. In addition, we describe investigations on the in vivo imaging of microglia using translocator protein (TSPO) PET and autoradiography, showing that microglial activation can occur in regions far remote from sites of focal injuries, in humans and animal models of TBI. Finally, we outline some novel potential therapeutic approaches that prime microglia/macrophages toward the beneficial restorative microglial phenotype after TBI.
AU  - Donat,CK
AU  - Scott,G
AU  - Gentleman,S
AU  - Sastre,M
DO  - 10.3389/fnagi.2017.00208
PY  - 2017///
SN  - 1663-4365
TI  - Microglial activation in traumatic brain injury
T2  - Frontiers in Aging Neuroscience
UR  - http://dx.doi.org/10.3389/fnagi.2017.00208
UR  - http://hdl.handle.net/10044/1/49119
VL  - 9
ER  -
Download