5-Lipoxygenase inhibitors potentiate 1alpha,25-dihydroxyvitamin D3-induced monocytic differentiation by activating p38 MAPK pathway

Mol Cell Biochem. 2009 Oct;330(1-2):229-38. doi: 10.1007/s11010-009-0138-x. Epub 2009 May 5.

Abstract

The treatment of human promyelocytic leukemia cell lines HL-60, and to some extent NB-4, with 1alpha,25-dihydroxyvitamin D(3) (VD3) induces differentiation toward the monocytic/macrophage lineage, demonstrated by the increased expression of CD11b and CD14, and the production of opsonized zymosan particles (OZP)-stimulated reactive oxygen species (ROS). Moreover, in more sensitive HL-60 cells, increased expression of 5-lipoxygenase (5-LPO), Mcl-1, IkappaB, and c-Jun, accompanied by the activation of p38 MAPK, was detected. These VD3 effects on HL-60 cell differentiation were significantly potentiated by 5-LPO inhibitors MK-886 and AA-861 and were inverted by SB202190 (SB), a p38 MAPK inhibitor. The inhibition of differentiation by SB was demonstrated by a reduction of CD14 expression and by a decrease in OZP-activated ROS production. These results indicated that p38 MAPK pathway is involved in 5-LPO inhibitors-dependent potentiation of VD3-induced monocytic differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arachidonate 5-Lipoxygenase / genetics*
  • Benzoquinones / pharmacology
  • Cell Differentiation / drug effects*
  • HL-60 Cells
  • Humans
  • Indoles / pharmacology
  • Lipoxygenase Inhibitors / pharmacology*
  • Monocytes / cytology*
  • Vitamin D / analogs & derivatives*
  • Vitamin D / pharmacology
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Benzoquinones
  • Indoles
  • Lipoxygenase Inhibitors
  • dihydroxy-vitamin D3
  • MK-886
  • Vitamin D
  • 2,3,5-trimethyl-6-(12-hydroxy-5,10-dodecadiynyl)-1,4-benzoquinone
  • Arachidonate 5-Lipoxygenase
  • p38 Mitogen-Activated Protein Kinases