SKAP2 acts downstream of CD11b/CD18 and regulates neutrophil effector function

Front Immunol. 2024 Feb 29:15:1344761. doi: 10.3389/fimmu.2024.1344761. eCollection 2024.

Abstract

Background: The importance of CD11b/CD18 expression in neutrophil effector functions is well known. Beyond KINDLIN3 and TALIN1, which are involved in the induction of the high-affinity binding CD11b/CD18 conformation, the signaling pathways that orchestrate this response remain incompletely understood.

Method: We performed an unbiased screening method for protein selection by biotin identification (BioID) and investigated the KINDLIN3 interactome. We used liquid chromatography with tandem mass spectrometry as a powerful analytical tool. Generation of NB4 CD18, KINDLIN3, or SKAP2 knockout neutrophils was achieved using CRISPR-Cas9 technology, and the cells were examined for their effector function using flow cytometry, live cell imaging, microscopy, adhesion, or antibody-dependent cellular cytotoxicity (ADCC).

Results: Among the 325 proteins significantly enriched, we identified Src kinase-associated phosphoprotein 2 (SKAP2), a protein involved in actin polymerization and integrin-mediated outside-in signaling. CD18 immunoprecipitation in primary or NB4 neutrophils demonstrated the presence of SKAP2 in the CD11b/CD18 complex at a steady state. Under this condition, adhesion to plastic, ICAM-1, or fibronectin was observed in the absence of SKAP2, which could be abrogated by blocking the actin rearrangements with latrunculin B. Upon stimulation of NB4 SKAP2-deficient neutrophils, adhesion to fibronectin was enhanced whereas CD18 clustering was strongly reduced. This response corresponded with significantly impaired CD11b/CD18-dependent NADPH oxidase activity, phagocytosis, and cytotoxicity against tumor cells.

Conclusion: Our results suggest that SKAP2 has a dual role. It may restrict CD11b/CD18-mediated adhesion only under resting conditions, but its major contribution lies in the regulation of dynamic CD11b/CD18-mediated actin rearrangements and clustering as required for cellular effector functions of human neutrophils.

Keywords: CD11b/CD18 integrin; Src kinase associated phosphoprotein 2 (SKAP2); adhesion; antibody-dependent cellular cytotoxicity (ADCC); filamentous actin; neutrophils; phagocytosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • CD18 Antigens / metabolism
  • Cell Adhesion
  • Fibronectins / metabolism
  • Humans
  • Macrophage-1 Antigen / metabolism
  • Neutrophils* / metabolism
  • Phosphoproteins / metabolism
  • src-Family Kinases* / metabolism

Substances

  • src-Family Kinases
  • Fibronectins
  • CD18 Antigens
  • Actins
  • Phosphoproteins
  • Macrophage-1 Antigen

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Dutch Cancer Society (grant number 11537).