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Cited by 394

The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.

Microglial Responses after Ischemic Stroke and Intracerebral Hemorrhage

Open access
Taylor, Roslyn A., Sansing, Lauren H.·2013·Clinical and Developmental Immunology

Abstract

Stroke is a leading cause of death worldwide. Ischemic stroke is caused by blockage of blood vessels in the brain leading to tissue death, while intracerebral hemorrhage (ICH) occurs when a blood vessel ruptures, exposing the brain to blood components. Both are associated with glial toxicity and neuroinflammation. Microglia, as the resident immune cells of the central nervous system (CNS), continually sample the environment for signs of injury and infection. Under homeostatic conditions, they have a ramified morphology and phagocytose debris. After stroke, microglia become activated, obtain an amoeboid morphology, and release inflammatory cytokines (the M1 phenotype). However, microglia can also be alternatively activated, performing crucial roles in limiting inflammation and phagocytosing tissue debris (the M2 phenotype). In rodent models, microglial activation occurs very early after stroke and ICH; however, their specific roles in injury and repair remain unclear. This review summarizes the literature on microglial responses after ischemic stroke and ICH, highlighting the mediators of microglial activation and potential therapeutic targets for each condition.

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Metadata

Authors
Taylor, R. A., & Sansing, L. H.
Venue
Clinical and Developmental Immunology
Publisher
Wiley
Published
2013
Volume
2013
Pages
1-10
ISSN
  • 1740-2522 (ISSN-L)
  • 1740-2530
OpenAlex
W2153168701
Cited by
394
References
12
FWCI
13.82
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Microglial Responses after Ischemic Stroke and Intracerebral Hemorrhage. https://app.cochat.ai/papers/10.1155/2013/746068
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Taylor, R. A., & Sansing, L. H. (2013). Microglial Responses after Ischemic Stroke and Intracerebral Hemorrhage. Clinical and Developmental Immunology. https://doi.org/10.1155/2013/746068

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.