Mild hypoxia triggers transient blood-brain barrier disruption: a fundamental protective role for microglia

Acta Neuropathol Commun. 2020 Oct 28;8(1):175. doi: 10.1186/s40478-020-01051-z.

Abstract

We recently demonstrated that when mice are exposed to chronic mild hypoxia (CMH, 8% O2), blood vessels in the spinal cord show transient vascular leak that is associated with clustering and activation of microglia around disrupted vessels. Importantly, microglial depletion profoundly increased hypoxia-induced vascular leak, implying that microglia play a critical role maintaining vascular integrity in the hypoxic spinal cord. The goal of the current study was to examine if microglia play a similar vasculo-protective function in the brain. Employing extravascular fibrinogen leak as an index of blood-brain barrier (BBB) disruption, we found that CMH provoked transient vascular leak in cerebral blood vessels that was associated with activation and aggregation of Mac-1-positive microglia around leaky vessels. Interestingly, CMH-induced vascular leak showed regional selectivity, being much more prevalent in the brainstem and olfactory bulb than the cerebral cortex and cerebellum. Pharmacological depletion of microglia with the colony stimulating factor-1 receptor inhibitor PLX5622, had no effect under normoxic conditions, but markedly increased hypoxia-induced cerebrovascular leak in all regions examined. As in the spinal cord, this was associated with endothelial induction of MECA-32, a marker of leaky CNS endothelium, and greater loss of endothelial tight junction proteins. Brain regions displaying the highest levels of hypoxic-induced vascular leak also showed the greatest levels of angiogenic remodeling, suggesting that transient BBB disruption may be an unwanted side-effect of hypoxic-induced angiogenic remodeling. As hypoxia is common to a multitude of human diseases including obstructive sleep apnea, lung disease, and age-related pulmonary, cardiac and cerebrovascular dysfunction, our findings have important translational implications. First, they point to a potential pathogenic role of chronic hypoxia in triggering BBB disruption and subsequent neurological dysfunction, and second, they demonstrate an important protective role for microglia in maintaining vascular integrity in the hypoxic brain.

Keywords: Angiogenesis; Blood vessels; Blood–brain barrier integrity; Brain; Chronic mild hypoxia; Endothelial proliferation; Fibrinogen; Microglia.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigens, Surface / metabolism
  • Blood-Brain Barrier / drug effects
  • Blood-Brain Barrier / metabolism*
  • Brain / blood supply
  • Brain / drug effects
  • Brain / metabolism*
  • Brain Stem / blood supply
  • Brain Stem / drug effects
  • Brain Stem / metabolism
  • Capillary Permeability / drug effects
  • Capillary Permeability / physiology*
  • Cerebellum / blood supply
  • Cerebellum / drug effects
  • Cerebellum / metabolism
  • Cerebral Cortex / blood supply
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism
  • Cerebrovascular Circulation
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism
  • Fibrinogen / metabolism*
  • Hypoxia / metabolism*
  • Hypoxia / physiopathology
  • Macrophage-1 Antigen / metabolism
  • Mice
  • Microglia / drug effects
  • Microglia / physiology*
  • Olfactory Bulb / blood supply
  • Olfactory Bulb / drug effects
  • Olfactory Bulb / metabolism
  • Organic Chemicals / pharmacology
  • Tight Junction Proteins / drug effects
  • Tight Junction Proteins / metabolism

Substances

  • Antigens, Surface
  • MECA-32 antigen, mouse
  • Macrophage-1 Antigen
  • Organic Chemicals
  • PLX5622
  • Tight Junction Proteins
  • Fibrinogen