MicroRNA-155 contributes to shear-resistant leukocyte adhesion to human brain endothelium in vitro

Fluids Barriers CNS. 2016 May 31;13(1):8. doi: 10.1186/s12987-016-0032-3.

Abstract

Background: Increased leukocyte adhesion to brain endothelial cells forming the blood-brain barrier (BBB) precedes extravasation into the central nervous system (CNS) in neuroinflammatory diseases such as multiple sclerosis (MS). Previously, we reported that microRNA-155 (miR-155) is up-regulated in MS and by inflammatory cytokines in human brain endothelium, with consequent modulation of endothelial paracellular permeability. Here, we investigated the role of endothelial miR-155 in leukocyte adhesion to the human cerebral microvascular endothelial cell line, hCMEC/D3, under shear forces mimicking blood flow in vivo.

Results: Using a gain- and loss-of-function approach, we show that miR-155 up-regulation increases leukocyte firm adhesion of both monocyte and T cells to hCMEC/D3 cells. Inhibition of endogenous endothelial miR-155 reduced monocytic and T cell firm adhesion to naïve and cytokines-induced human brain endothelium. Furthermore, this effect is partially associated with modulation of the endothelial cell adhesion molecules VCAM1 and ICAM1 by miR-155.

Conclusions: Our results suggest that endothelial miR-155 contribute to the regulation of leukocyte adhesion at the inflamed BBB. Taken together with previous observations, brain endothelial miR-155 may constitute a potential molecular target for treatment of neuroinflammation diseases.

Keywords: Blood–brain barrier; Cell adhesion molecules; Flow shear stress; Leukocyte adhesion; Neuroinflammation; microRNA-155.

MeSH terms

  • Blood-Brain Barrier / metabolism*
  • Cell Adhesion / physiology*
  • Cell Line
  • Cerebrovascular Circulation / physiology
  • Endothelial Cells / metabolism*
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism
  • Jurkat Cells
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Models, Cardiovascular
  • Models, Neurological
  • Monocytes / metabolism*
  • Neuroimmunomodulation / physiology
  • Shear Strength / physiology
  • T-Lymphocytes / metabolism*
  • Transfection
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • ICAM1 protein, human
  • MIRN155 microRNA, human
  • MicroRNAs
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1