Ecto-5'-nucleotidase/CD73 enhances endothelial barrier function and sprouting in blood but not lymphatic vasculature

Eur J Immunol. 2015 Feb;45(2):562-73. doi: 10.1002/eji.201444856. Epub 2014 Dec 15.

Abstract

CD73/ecto-5'-nucleotidase is a key enzyme in the regulation of purinergic signaling and inflammatory reactions. It hydrolyzes extracellular AMP into adenosine, which dampens immune cell activation, and reduces leukocyte trafficking. By comparing CD73 expression and function in mononuclear and endothelial cells (ECs) of blood and lymph, we show that extracellular purines and CD73 activity have differential effects in these two vascular systems. We found that CD8-positive T lymphocytes and CD19-positive B lymphocytes in human lymph expressed high levels of CD73 and other purinergic enzymes and adenosine receptors. Soluble CD73 was less abundant in human lymph than in serum, whereas CD73 activity was higher in afferent lymphatic ECs than in blood ECs. Adenosine signaling improved barrier function and induced sprouting of human blood, but not lymphatic, ECs in vitro. Similarly, using CD73-deficient mice we found that CD73 controls only blood vascular permeability at selected lymphoid organs under physiological conditions. Thus, both vascular and lymphatic arms of the immune system synthesize the components of purinergic signaling system, but surprisingly they use CD73 differentially to control endothelial permeability and sprouting.

Keywords: adenosine; endothelial cells; lymphatics; permeability; purinergic signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5'-Nucleotidase / deficiency
  • 5'-Nucleotidase / genetics
  • 5'-Nucleotidase / immunology*
  • Adenosine / immunology*
  • Adenosine / metabolism
  • Adenosine Monophosphate / immunology
  • Adenosine Monophosphate / metabolism
  • Animals
  • Antigens, CD19 / genetics
  • Antigens, CD19 / immunology
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism
  • Capillary Permeability / immunology*
  • Endothelial Cells / cytology
  • Endothelial Cells / immunology
  • Endothelial Cells / metabolism
  • Endothelium, Lymphatic / cytology
  • Endothelium, Lymphatic / immunology*
  • Endothelium, Lymphatic / metabolism
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / immunology*
  • Endothelium, Vascular / metabolism
  • Gene Expression
  • Humans
  • Immunity, Innate
  • Mice
  • Mice, Knockout
  • Neovascularization, Physiologic
  • Organ Specificity
  • Receptors, Purinergic P1 / genetics
  • Receptors, Purinergic P1 / immunology
  • Signal Transduction

Substances

  • Antigens, CD19
  • Receptors, Purinergic P1
  • Adenosine Monophosphate
  • 5'-Nucleotidase
  • Adenosine