Neutrophil priming: pathophysiological consequences and underlying mechanisms

Clin Sci (Lond). 1998 May;94(5):461-71. doi: 10.1042/cs0940461.


1. Neutrophil priming by agents such as tumour necrosis factor-alpha, granulocyte/macrophage colony-stimulating factor and lipopolysaccharide causes a dramatic increase in the response of these cells to an activating agent; this process has been shown to be critical for neutrophil-mediated tissue injury both in vitro and in vivo. 2. The principle consequence of priming, aside from a direct effect on cell polarization, deformability and integrin/selectin expression, is to permit secretagogue-induced superoxide anion generation, degranulation and lipid mediator (e.g. leukotriene B4 and arachidonic acid) release. It is now recognized that most priming agents also serve an additional function of delaying apoptosis and hence increasing the functional longevity of these cells at the inflamed site. 3. The potential mechanisms underlying priming are discussed; current data suggest a dissociation between priming and changes in receptor number and/or affinity, G-protein expression, phospholipase C and phospholipase A2 activation and changes in intracellular Ca2+ concentration. However, more recent studies support a key role for protein tyrosine phosphorylation and enhanced phospholipase D and phosphoinositide 3-kinase activity in neutrophil priming. 4. Recent work has also revealed the potential for neutrophils to spontaneously and fully 'de-prime' after an initial challenge with platelet-activating factor. This ability of neutrophils to undergo a complete cycle of priming-de-priming (and re-priming) reveals a previously unrecognized flexibility in the control of neutrophil behaviour at an inflamed site.

Publication types

  • Editorial
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Enzyme Activation
  • GTP-Binding Proteins / metabolism
  • Humans
  • Inflammation / immunology*
  • Inflammation Mediators / physiology*
  • Neutrophil Activation*
  • Neutrophils / drug effects*
  • Neutrophils / physiology
  • Phospholipase D / metabolism
  • Respiratory Burst
  • Type C Phospholipases / metabolism


  • Inflammation Mediators
  • Type C Phospholipases
  • Phospholipase D
  • GTP-Binding Proteins