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Temporal and Spatial Dynamics of Cerebral Immune Cell Accumulation in Stroke

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TLDR
The peculiar activation pattern and massive increase of antigen-presenting cells in temporal conjunction with regulatory cells might provide additional insight into poststroke immune regulation.
Abstract
Background and Purpose— Ischemic stroke leads to significant morbidity and mortality in the Western world Early reperfusion strategies remain the treatment of choice but can initiate and augment an inflammatory response causing secondary brain damage The understanding of postischemic inflammation is very limited The objectives of this study were to define the temporal and spatial infiltration of immune cell populations and their activation patterns in a murine cerebral ischemia–reperfusion injury model Methods— Transient middle cerebral artery occlusion was induced for 1 hour followed by 12-hour to 7-day reperfusion in C57/BL6 mice Immunohistochemistry and flow cytometry were used to quantify the infiltrating immune cell subsets Results— Accumulation of microglia and infiltration of the ischemic hemisphere by macrophages, lymphocytes, and dendritic cells (DCs) preceded the neutrophilic influx DCs were found to increase 20-fold and constituted a substantial proportion of infiltrating cells DCs exhi

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Citations
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Journal ArticleDOI

Regulatory T Cell in Stroke: A New Paradigm for Immune Regulation

TL;DR: Evidence of FoxP3+CD25+CD4+ Tregs as potentially important immunomodulators in stroke pathogenesis is summarized and further investigations for possible immunotherapeutic strategies by modulating the quantity and/or functional effects of FoxTregs in stroke patients are highlighted.
Journal ArticleDOI

Inflammatory cell recruitment after experimental thromboembolic stroke in rats.

TL;DR: This study provides novel data on the local inflammatory response to experimental thromboembolic stroke using a rodent model of stroke that closely reflects human embolic ischemia and recommends that future stroke research should preferably use animal models with relevance for clinical translation.
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Non-invasive tracking of CD4+ T cells with a paramagnetic and fluorescent nanoparticle in brain ischemia

TL;DR: In this paper, an in-vivo imaging approach for sequential monitoring of brain-infiltrating CD4+ T cells in experimental ischemic stroke was described, where magnetic resonance imaging (MRI) or Xenogen imaging combined with labeling of SPIO-Molday ION Rhodamine-B (MIRB) can be used to monitor the dynamics of CD4(+) T cells.
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The Role of Gamma-Delta T Cells in Diseases of the Central Nervous System.

TL;DR: A review of the neuro-inflammatory and immune functions of γδ T cells is offered, intending to understand their roles in CNS diseases, which may be crucial for the development of novel clinical applications.
Journal ArticleDOI

Single-cell RNA-seq reveals the transcriptional landscape in ischemic stroke:

TL;DR: In this paper, the authors employed single-cell RNA sequencing (scRNA-seq) to comprehensively map the cell populations in the mouse model of MCAO (middle cerebral artery occlusion).
References
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Journal ArticleDOI

Pathobiology of ischaemic stroke: an integrated view

TL;DR: This article provides a framework that can be used to generate testable hypotheses and treatment strategies that are linked to the appearance of specific pathophysiological events within the ischaemic brain.
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Microglia: active sensor and versatile effector cells in the normal and pathologic brain

TL;DR: This review focuses on several key observations that illustrate the multi-faceted activities of microglia in the normal and pathologic brain.
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Taking dendritic cells into medicine

TL;DR: Some medical implications of DC biology that account for illness and provide opportunities for prevention and therapy are presented.
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The inflammatory response in stroke.

TL;DR: The role of specific cell types including leukocytes, endothelium, glia, microglia, the extracellular matrix and neurons, and mediators produced by inflammatory cells such as cytokines, chemokines, reactive oxygen species and arachidonic acid metabolites are reviewed.
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A synthetic glycolipid prevents autoimmune encephalomyelitis by inducing TH2 bias of natural killer T cells.

TL;DR: A synthetic glycolipid ligand for CD1d-restricted natural killer T (NKT) cells expressing the semi-invariant T-cell receptor (Vα14+) is preventive against EAE and targeting NKT cells with this ligand may be an attractive means for intervening in human autoimmune diseases such as multiple sclerosis.
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