Interaction of kindlin-3 and β2-integrins differentially regulates neutrophil recruitment and NET release in mice

Blood. 2015 Jul 16;126(3):373-7. doi: 10.1182/blood-2015-03-636720. Epub 2015 Jun 8.

Abstract

Kindlin-3 essentially supports integrin activation in blood cells. Absence of kindlin-3 in humans causes leukocyte adhesion deficiency-III characterized with severe bleeding disorder and recurrent infections. Previously, we generated kindlin-3 knock-in (K3KI) mice carrying an integrin-interaction disrupting mutation in kindlin-3 and verified the functional significance of the binding of kindlin-3 to integrin αIIbβ3 in platelets. Here, using K3KI mice, we functionally evaluate the crosstalk between kindlin-3 and β2-integrins in neutrophils. Although the kindlin-3 mutant in K3KI neutrophils is normally expressed, its binding ability to β2-integrins in neutrophils is disabled. In vitro and in vivo analyses disclose that β2-integrin-mediated K3KI neutrophil adhesion and recruitment are significantly suppressed. Interestingly, the ability of releasing neutrophil extracellular traps (NETs) from K3KI neutrophils is also compromised. Substantially, a peptide derived from the integrin β2 cytoplasmic tail that can inhibit the interaction between kindlin-3 and β2-inegrins significantly jeopardizes NET release without affecting neutrophil adhesion and recruitment under the experimental conditions. These findings suggest that crosstalk between kindlin-3 and β2-integrins in neutrophils is required for supporting both neutrophil recruitment and NET release, but the involved regulatory mechanisms in these two cellular events might be differential, thus providing a novel therapeutic concept to treat innate immune-related diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Platelets / cytology
  • Blood Platelets / immunology*
  • Blood Platelets / metabolism
  • Blotting, Western
  • CD18 Antigens / immunology
  • CD18 Antigens / metabolism*
  • Cell Adhesion
  • Cells, Cultured
  • Cytoskeletal Proteins / immunology
  • Cytoskeletal Proteins / metabolism*
  • Flow Cytometry
  • Mice
  • Neutrophil Infiltration / immunology*
  • Neutrophils / cytology
  • Neutrophils / immunology*
  • Neutrophils / metabolism

Substances

  • CD18 Antigens
  • Cytoskeletal Proteins
  • kindlin-3 protein, mouse