Regulation of blood-brain barrier integrity by microglia in health and disease: A therapeutic opportunity.

TitleRegulation of blood-brain barrier integrity by microglia in health and disease: A therapeutic opportunity.
Publication TypeJournal Article
Year of Publication2020
AuthorsRonaldson PT, Davis TP
JournalJ Cereb Blood Flow Metab
Date Published2020 Dec
KeywordsBlood-Brain Barrier, Humans, Microglia, Oxidative Stress

The blood-brain barrier (BBB) is a critical regulator of CNS homeostasis. It possesses physical and biochemical characteristics (i.e. tight junction protein complexes, transporters) that are necessary for the BBB to perform this physiological role. Microvascular endothelial cells require support from astrocytes, pericytes, microglia, neurons, and constituents of the extracellular matrix. This intricate relationship implies the existence of a neurovascular unit (NVU). NVU cellular components can be activated in disease and contribute to dynamic remodeling of the BBB. This is especially true of microglia, the resident immune cells of the brain, which polarize into distinct proinflammatory (M1) or anti-inflammatory (M2) phenotypes. Current data indicate that M1 pro-inflammatory microglia contribute to BBB dysfunction and vascular "leak", while M2 anti-inflammatory microglia play a protective role at the BBB. Understanding biological mechanisms involved in microglia activation provides a unique opportunity to develop novel treatment approaches for neurological diseases. In this review, we highlight characteristics of M1 proinflammatory and M2 anti-inflammatory microglia and describe how these distinct phenotypes modulate BBB physiology. Additionally, we outline the role of other NVU cell types in regulating microglial activation and highlight how microglia can be targeted for treatment of disease with a focus on ischemic stroke and Alzheimer's disease.

Alternate JournalJ Cereb Blood Flow Metab
PubMed ID32928017
PubMed Central IDPMC7687032
Grant ListR01 DA051812 / DA / NIDA NIH HHS / United States
R01 NS084941 / NS / NINDS NIH HHS / United States
Faculty Member Reference: 
Thomas P Davis, PhD
Patrick T Ronaldson, PhD, FAAPS