The 5-lipoxygenase pathway regulates vasculogenesis in differentiating mouse embryonic stem cells

Cardiovasc Res. 2010 Apr 1;86(1):37-44. doi: 10.1093/cvr/cvp385. Epub 2009 Dec 4.

Abstract

Aims: It is well established that leukotrienes (LTs), products of the 5-lipoxygenase (5-LO) pathway, participate in inflammatory tissue reactions and immune responses. In the present study, the impact of the 5-LO pathway on vasculogenesis of mouse embryonic stem (ES) cells was investigated.

Methods and results: Immunohistochemistry studies demonstrated that 5-LO(+) cells first appeared at day 6 of embryoid body (EB) formation from ES cells. 5-LO(+)/CD68(+) as well as 5-LO(+)/CD45(+) cells were prominent at day 10 of EB differentiation. Real-time PCR and western blot analysis revealed all constituents of the 5-LO pathway. High performance liquid chromatography analyses indicated the synthesis of LTB(4) and LTD(4) in conformity with induction of the 5-LO pathway. Furthermore, Flk-1(+)/CD105(+) cells displayed calcium- (Ca(2+)) transients in response to LTB(4), whereas CD11b(+) cells responded to LTD(4). Treatment of EBs with LTB(4) and LTD(4) resulted in phosphorylation of the mitogen-activated protein kinase ERK1/2. Pharmacological inhibition of the 5-LO pathway and stable shRNA targeting of 5-LO-activating protein decreased capillary cell areas positive for PECAM-1.

Conclusion: Our data demonstrate that the 5-LO pathway emerges early during ES cell differentiation into cells of the myeloid lineage and that LTs play an until now unrecognized role in vascular development of ES cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5-Lipoxygenase-Activating Proteins
  • Animals
  • Arachidonate 5-Lipoxygenase / genetics
  • Arachidonate 5-Lipoxygenase / metabolism*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Differentiation / physiology
  • Cell Lineage / physiology
  • Cells, Cultured
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / drug effects
  • Embryonic Stem Cells / enzymology*
  • Epoxide Hydrolases / genetics
  • Epoxide Hydrolases / metabolism
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Glutathione Transferase / genetics
  • Glutathione Transferase / metabolism
  • Leukotriene B4 / pharmacology
  • Leukotriene D4 / pharmacology
  • Leukotrienes / metabolism
  • Lymphocytes / cytology
  • Lymphocytes / physiology
  • Macrophages / cytology
  • Macrophages / physiology
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Neovascularization, Pathologic / immunology
  • Neovascularization, Pathologic / metabolism*
  • Neovascularization, Pathologic / pathology
  • Phosphorylation / drug effects
  • Phosphorylation / physiology
  • RNA, Messenger / metabolism
  • RNA, Small Interfering
  • Receptors, Leukotriene / genetics
  • Receptors, Leukotriene / metabolism
  • Receptors, Leukotriene B4 / genetics
  • Receptors, Leukotriene B4 / metabolism
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism

Substances

  • 5-Lipoxygenase-Activating Proteins
  • Alox5ap protein, mouse
  • Carrier Proteins
  • Leukotrienes
  • Ltb4r1 protein, mouse
  • Ltb4r2 protein, mouse
  • Membrane Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Receptors, Leukotriene
  • Receptors, Leukotriene B4
  • Leukotriene B4
  • Leukotriene D4
  • cysteinyl leukotriene receptor 2
  • Arachidonate 5-Lipoxygenase
  • Glutathione Transferase
  • Vascular Endothelial Growth Factor Receptor-2
  • Extracellular Signal-Regulated MAP Kinases
  • Epoxide Hydrolases
  • leukotriene-C4 synthase
  • leukotriene D4 receptor
  • leukotriene A4 hydrolase