Inflammation within the neurovascular unit: Focus on microglia for stroke injury and recovery.

Pharmacol Res

Ralph Johnson VA Medical Center, Medical University of South Carolina, Charleston, SC, United States; Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, United States. Electronic address:

Published: September 2019

AI Article Synopsis

  • Neuroinflammation is a key factor in neurodegenerative diseases and stroke, with microglia acting as crucial responders to brain injuries while also serving other important functions.
  • Recent research suggests that instead of trying to eliminate microglia, we should focus on modulating their activities for better outcomes.
  • The review highlights microglial roles, their interactions with the neurovascular unit, differences based on sex, and how conditions like hypertension and diabetes affect their response in cases of ischemic stroke.

Article Abstract

Neuroinflammation underlies the etiology of multiple neurodegenerative diseases and stroke. Our understanding of neuroinflammation has evolved in the last few years and major players have been identified. Microglia, the brain resident macrophages, are considered sentinels at the forefront of the neuroinflammatory response to different brain insults. Interestingly, microglia perform other physiological functions in addition to their role in neuroinflammation. Therefore, an updated approach in which modulation, rather than complete elimination of microglia is necessary. In this review, the emerging roles of microglia and their interaction with different components of the neurovascular unit are discussed. In addition, recent data on sex differences in microglial physiology and in the context of stroke will be presented. Finally, the multiplicity of roles assumed by microglia in the pathophysiology of ischemic stroke, and in the presence of co-morbidities such as hypertension and diabetes are summarized.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954670PMC
http://dx.doi.org/10.1016/j.phrs.2019.104349DOI Listing

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