Schwarzmaier Susanne M, Plesnila Nikolaus
Department of Anesthesiology, University of Munich Medical Center Munich, Germany ; Institute for Stroke and Dementia Research (ISD), University of Munich Medical Center Munich, Germany.
Institute for Stroke and Dementia Research (ISD), University of Munich Medical Center Munich, Germany ; Munich Cluster of Systems Neurology Munich, Germany.
Front Cell Neurosci. 2014 Nov 4;8:358. doi: 10.3389/fncel.2014.00358. eCollection 2014.
Traumatic brain injury (TBI) results in immediate brain damage that is caused by the mechanical impact and is non-reversible. This initiates a cascade of delayed processes which cause additional-secondary-brain damage. Among these secondary mechanisms, the inflammatory response is believed to play an important role, mediating actions that can have both protective and detrimental effects on the progression of secondary brain damage. Histological data generated extensive information; however, this is only a snapshot of processes that are, in fact, very dynamic. In contrast, in vivo microscopy provides detailed insight into the temporal and spatial patterns of cellular dynamics. In this review, we aim to summarize data which was generated by in vivo microscopy, specifically investigating the immune response following brain trauma, and its potential effects on secondary brain damage.
创伤性脑损伤(TBI)会导致由机械冲击引起的即时性脑损伤,且这种损伤是不可逆的。这会引发一系列延迟过程,导致额外的继发性脑损伤。在这些继发性机制中,炎症反应被认为起着重要作用,介导着对继发性脑损伤进展既有保护作用又有有害作用的行为。组织学数据产生了大量信息;然而,这只是实际上非常动态的过程的一个快照。相比之下,体内显微镜检查能深入了解细胞动态的时空模式。在本综述中,我们旨在总结由体内显微镜检查产生的数据,特别研究脑外伤后的免疫反应及其对继发性脑损伤的潜在影响。