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Multiple Phenotypic Changes Define Neutrophil Priming.

Irina Miralda1, Silvia M Uriarte1,2, Kenneth R McLeish2,3

  • 1Department of Microbiology, University of Louisville School of MedicineLouisville, KY, United States.

Frontiers in Cellular and Infection Microbiology
|June 15, 2017
PubMed
Summary
This summary is machine-generated.

Neutrophil priming involves enhanced responses and activated functions beyond reactive oxygen species (ROS) generation. This state significantly impacts innate and adaptive immunity, suggesting a broader definition is needed.

Keywords:
apoptosischemotaxiscytokinesexocytosisneutrophilsphagocytosisprimingrespiratory burst

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Area of Science:

  • Immunology
  • Cellular Biology
  • Molecular Mechanisms

Background:

  • Neutrophils transition from a basal to a primed state upon exposure to various immune stimuli.
  • Priming is traditionally defined by enhanced reactive oxygen species (ROS) generation via NADPH oxidase.

Purpose of the Study:

  • To review the diverse phenotypic changes associated with neutrophil priming.
  • To explore the molecular mechanisms underlying these changes.
  • To propose a revised, broader definition of neutrophil priming.

Main Methods:

  • Literature review of studies on neutrophil priming.
  • Analysis of phenotypic and functional alterations in primed neutrophils.
  • Examination of molecular pathways involved in neutrophil priming.

Main Results:

  • Primed neutrophils exhibit enhanced responsiveness in exocytosis, NET formation, and chemotaxis.
  • Phenotypic changes include activated adhesion, transcription, metabolism, and apoptosis.
  • Molecular mechanisms driving these diverse changes are actively being elucidated.

Conclusions:

  • The current definition of neutrophil priming is too restrictive.
  • Priming encompasses both enhanced responsiveness and activated functions.
  • This broader understanding is crucial for regulating innate and adaptive immune responses.