The HIF-1/glial TIM-3 axis controls inflammation-associated brain damage under hypoxia

Nat Commun. 2015 Mar 20:6:6340. doi: 10.1038/ncomms7340.

Abstract

Inflammation is closely related to the extent of damage following cerebral ischaemia, and the targeting of this inflammation has emerged as a promising therapeutic strategy. Here, we present that hypoxia-induced glial T-cell immunoglobulin and mucin domain protein (TIM)-3 can function as a modulator that links inflammation and subsequent brain damage after ischaemia. We find that TIM-3 is highly expressed in hypoxic brain regions of a mouse cerebral hypoxia-ischaemia (H/I) model. TIM-3 is distinctively upregulated in activated microglia and astrocytes, brain resident immune cells, in a hypoxia-inducible factor (HIF)-1-dependent manner. Notably, blockade of TIM-3 markedly reduces infarct size, neuronal cell death, oedema formation and neutrophil infiltration in H/I mice. Hypoxia-triggered neutrophil migration and infarction are also decreased in HIF-1α-deficient mice. Moreover, functional neurological deficits after H/I are significantly improved in both anti-TIM-3-treated mice and myeloid-specific HIF-1α-deficient mice. Further understanding of these insights could serve as the basis for broadening the therapeutic scope against hypoxia-associated brain diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / immunology*
  • Brain / immunology*
  • Brain / pathology
  • Carotid Artery, Common / surgery
  • Cell Movement
  • Cells, Cultured
  • Hepatitis A Virus Cellular Receptor 2
  • Hypoxia-Inducible Factor 1, alpha Subunit / immunology*
  • Hypoxia-Ischemia, Brain / immunology*
  • Hypoxia-Ischemia, Brain / pathology
  • Immunohistochemistry
  • In Vitro Techniques
  • Inflammation
  • Ligation
  • Magnetic Resonance Imaging
  • Mesencephalon
  • Mice
  • Microglia / immunology*
  • Neuroglia / immunology
  • Neutrophils
  • RNA, Messenger / metabolism*
  • Receptors, Virus / immunology*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Havcr2 protein, mouse
  • Hepatitis A Virus Cellular Receptor 2
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • RNA, Messenger
  • Receptors, Virus