Neuroinflammation after intracerebral hemorrhage

Spontaneous intracerebral haemorrhage (ICH) is a particularly severe type of stroke for which no specific treatment has been established yet. Although preclinical models of ICH have substantial methodological limitations, important insight into the pathophysiology has been gained. Mounting evidence...

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Bibliographic Details
Main Authors: Mracskó, Eva (Author) , Veltkamp, Roland (Author)
Format: Article (Journal)
Language:English
Published: 20 November 2014
In: Frontiers in cellular neuroscience
Year: 2014, Volume: 8
ISSN:1662-5102
DOI:10.3389/fncel.2014.00388
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3389/fncel.2014.00388
Verlag, lizenzpflichtig, Volltext: https://www.frontiersin.org/articles/10.3389/fncel.2014.00388/full
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Author Notes:Eva Mracsko and Roland Veltkamp
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Summary:Spontaneous intracerebral haemorrhage (ICH) is a particularly severe type of stroke for which no specific treatment has been established yet. Although preclinical models of ICH have substantial methodological limitations, important insight into the pathophysiology has been gained. Mounting evidence suggests an important contribution of inflammatory mechanisms to brain damage and potentially repair. Neuroinflammation evoked by intracerebral blood involves the activation of resident microglia, the infiltration of systemic immune cells and the production of cytokines, chemokines extracellular proteases and reactive oxygen species. Previous studies focused on innate immunity including microglia, monocytes and granulocytes. More recently, the role of adaptive immune cells has received increasing attention. Little is currently known about the interactions among different immune cell populations in the setting of ICH. Nevertheless, immunomodulatory strategies are already being explored in ICH. To improve the chances of translation from preclinical models to patients, a better characterization of the neuroinflammation in patients is desirable.
Item Description:Gesehen am 28.07.2020
Physical Description:Online Resource
ISSN:1662-5102
DOI:10.3389/fncel.2014.00388