5-Lipoxygenase products regulate basophil functions: 5-Oxo-ETE elicits migration, and leukotriene B(4) induces degranulation

J Allergy Clin Immunol. 2005 Sep;116(3):578-85. doi: 10.1016/j.jaci.2005.04.029.

Abstract

Background: 5-Lipoxygenase (5-LO) products have been strongly implicated in the pathogenesis of allergic diseases. In addition to their physiologic effects on residential cells, 5-LO products are capable of stimulating various eosinophil functions. However, little is known regarding the effects of 5-LO products on basophil functions.

Objective: This study was designed to elucidate the effects of the main 5-LO products (ie, leukotriene [LT] B(4), LTD(4), and 5-oxo-6,8,11,14-eicosatetraenoic acid [5-oxo-ETE]), as well as their receptor expression on human basophils.

Methods: We studied the effects of 5-LO products on Ca(2+) mobilization, migration, CD 11b expression, and degranulation of human basophils. Expression of the receptors for LTC(4)/D(4)/E(4) (cysteinyl leukotriene 1 [CysLT(1)] and CysLT(2)), LTB4 (BLT(1) and BLT(2)), and 5-oxo-ETE (oxoeicosanoid [OXE]) was assessed by means of real-time PCR and flow cytometry.

Results: At the mRNA level, basophils strongly expressed OXE and predominantly expressed CysLT(1) and BLT(2). The expression level of OXE mRNA in basophils was approximately 20-fold higher than in neutrophils and similar to that in eosinophils. At the protein level, basophils expressed CysLT(1), CysLT(2), BLT(1), and OXE, but not BLT(2). All products elicited a transient increase of cytosolic calcium, with the order of magnitude being LTB(4)>5-oxo-ETE>LTD(4). 5-Oxo-ETE induced a strong basophil migratory response that was almost equivalent to that of prostaglandin D(2). LTB(4) elicited significant degranulation of IL-3-primed basophils. In contrast, no functional significance was observed for LTD(4).

Conclusion: Among 5-LO products, 5-oxo-ETE induces a potent basophil migratory response, and LTB(4) elicits degranulation under certain conditions. Our results strongly suggest that 5-oxo-ETE might afford opportunities for therapeutic targeting in allergic inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arachidonate 5-Lipoxygenase / immunology
  • Arachidonate 5-Lipoxygenase / metabolism*
  • Arachidonic Acids / immunology
  • Arachidonic Acids / metabolism*
  • Basophil Degranulation Test
  • Basophils / immunology
  • Basophils / metabolism*
  • Calcium / metabolism
  • Cell Degranulation / immunology*
  • Cell Movement / immunology*
  • Chemotactic Factors / immunology
  • Chemotactic Factors / metabolism
  • Eicosanoids / immunology
  • Eicosanoids / metabolism
  • Flow Cytometry
  • Humans
  • Leukotriene B4 / immunology
  • Leukotriene B4 / metabolism*
  • RNA, Messenger / analysis
  • Receptors, Eicosanoid / immunology
  • Receptors, Eicosanoid / metabolism
  • Receptors, Leukotriene / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Arachidonic Acids
  • Chemotactic Factors
  • Eicosanoids
  • RNA, Messenger
  • Receptors, Eicosanoid
  • Receptors, Leukotriene
  • 5-oxo-6,8,11,14-eicosatetraenoic acid
  • Leukotriene B4
  • Arachidonate 5-Lipoxygenase
  • Calcium