4.8 Article

Differential regulation of Type 1 and Type 2 mouse eosinophil activation by apoptotic cells

Journal

FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.1041660

Keywords

eosinophils; allergy; inflammation; IL-4; IFN-gamma; apoptotic cells

Categories

Funding

  1. US-Israel Bi-national Science Foundation [2015163, 2015045]
  2. Israel Science Foundation [886/15, 542/20]
  3. Israel Cancer Research Fund
  4. Richard Eimert Research Fund on Solid Tumors
  5. Israel Cancer Association
  6. Dotan Hemato Oncology Fund
  7. Cancer Biology Research Center
  8. Tel Aviv University
  9. Tel Aviv University Faculty of Medicine Recanati Fund
  10. Azrieli Foundation Canada-Israel
  11. Aimwell Charitable Trust (UK)
  12. Dir for Tech, Innovation, & Partnerships [2015163] Funding Source: National Science Foundation
  13. Translational Impacts [2015163] Funding Source: National Science Foundation

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This study demonstrates that eosinophils can interact with apoptotic cells, leading to polarized activation towards an anti-inflammatory phenotype. Apoptotic cells suppress the inflammatory responses of eosinophils and enhance the activation induced by specific cytokines. These findings reveal the heterogeneity of eosinophil activation patterns and highlight the potential role of apoptotic cells in regulating eosinophil polarization.
Eosinophils are multifunctional, evolutionary conserved leukocytes that are involved in a plethora of responses ranging from regulation of tissue homeostasis, host defense and cancer. Although eosinophils have been studied mostly in the context of Type 2 inflammatory responses, it is now evident that they participate in Type 1 inflammatory responses and can respond to Type 1 cytokines such as IFN-gamma. Notably, both Type 1- and Type 2 inflammatory environments are characterized by tissue damage and cell death. Collectively, this raises the possibility that eosinophils can interact with apoptotic cells, which can alter eosinophil activation in the inflammatory milieu. Herein, we demonstrate that eosinophils can bind and engulf apoptotic cells. We further show that exposure of eosinophils to apoptotic cells induces marked transcriptional changes in eosinophils, which polarize eosinophils towards an anti-inflammatory phenotype that is associated with wound healing and cell migration. Using an unbiased RNA sequencing approach, we demonstrate that apoptotic cells suppress the inflammatory responses of eosinophils that were activated with IFN-gamma + E. coli (e.g., Type 1 eosinophils) and augment IL-4-induced eosinophil activation (e.g., Type 2 eosinophils). These data contribute to the growing understanding regarding the heterogeneity of eosinophil activation patterns and highlight apoptotic cells as potential regulators of eosinophil polarization.

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