The synapse in traumatic brain injury

被引:121
作者
Jamjoom, Aimun A. B. [1 ]
Rhodes, Jonathan [2 ]
Andrews, Peter J. D. [2 ]
Grant, Seth G. N. [1 ,3 ]
机构
[1] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh BioQuarter, Chancellors Bldg, Edinburgh EH16 4SB, Midlothian, Scotland
[2] Univ Edinburgh, Anaesthesia Crit Care & Pain Med, Edinburgh EH16 4SA, Midlothian, Scotland
[3] Univ Edinburgh, Ctr Discovery Brain Sci, Simons Initiat Developing Brain SIDB, Hugh Robson Bldg,George Sq, Edinburgh EH8 9XD, Midlothian, Scotland
基金
英国惠康基金; 欧洲研究理事会;
关键词
synaptopathy; synaptome; astrocyte; inflammation; microglia; OXIDATIVE STRESS; POSTSYNAPTIC DENSITY; CEREBROSPINAL-FLUID; PROTEOMIC ANALYSIS; AXONAL INJURY; PET TRACER; REACTIVE SYNAPTOGENESIS; ALZHEIMERS-DISEASE; DENDRITIC SPINES; CORTICAL IMPACT;
D O I
10.1093/brain/awaa321
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Traumatic brain injury (TBI) is a leading cause of death and disability worldwide and is a risk factor for dementia later in life. Research into the pathophysiology of TBI has focused on the impact of injury on the neuron. However, recent advances have shown that TBI has a major impact on synapse structure and function through a combination of the immediate mechanical insult and the ensuing secondary injury processes, leading to synapse loss. In this review, we highlight the role of the synapse in TBI pathophysiology with a focus on the confluence of multiple secondary injury processes including excitotoxicity, inflammation and oxidative stress. The primary insult triggers a cascade of events in each of these secondary processes and we discuss the complex interplay that occurs at the synapse. We also examine how the synapse is impacted by traumatic axonal injury and the role it may play in the spread of tau after TBI. We propose that astrocytes play a crucial role by mediating both synapse loss and recovery. Finally, we highlight recent developments in the field including synapse molecular imaging, fluid biomarkers and therapeutics. In particular, we discuss advances in our understanding of synapse diversity and suggest that the new technology of synaptome mapping may prove useful in identifying synapses that are vulnerable or resistant to TBI.
引用
收藏
页码:18 / 31
页数:14
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