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Leukotriene D4 stimulates the migration but not proliferation of endothelial cells mediated by the cysteinyl leukotriene cyslt(1) receptor via the extracellular signal-regulated kinase pathway. | LitMetric

AI Article Synopsis

  • Cysteinyl leukotrienes (CysLTs) activate specific CysLT receptors, particularly CysLT(1), which influences vascular responses; however, their role in the proliferation and movement of endothelial cells remains unclear.
  • In a study using EA.hy926 endothelial cells, LTD(4), a type of CysLT, was found to significantly enhance cell migration but did not affect cell proliferation, while also increasing ERK1/2 phosphorylation.
  • The migration induced by LTD(4) was effectively blocked by CysLT(1) receptor antagonists and an ERK1/2 inhibitor, suggesting that CysLT(1) receptor-mediated migration of endothelial cells is regulated through the ERK1/

Article Abstract

The actions of cysteinyl leukotrienes (CysLTs) are mediated by activating CysLT receptors, CysLT(1), and CysLT(2). The CysLT(1) receptor mediates vascular responses to CysLTs; however, its effect on the proliferation and migration of endothelial cells is not clarified. To determine this effect, we observed proliferation and migration in EA.hy926 cells, a human endothelial cell line, and the involvement of activation of mitogen-activated protein kinases (MAPKs). We found that LTD(4) did not affect the proliferation, but significantly stimulated the migration of endothelial cells. LTD(4) also induced the phosphorylation of extracellular signal-regulated kinase (ERK) 1/2, but not those of p38 or JNK. The LTD(4)-induced migration and ERK1/2 phosphorylation were blocked by the CysLT(1)-receptor antagonist montelukast and the dual antagonist Bay u9773, but not by the CysLT(2)-receptor antagonist Bay cysLT2; the migration was also inhibited by the ERK1/2 inhibitor U0126. Our findings indicate that LTD(4) stimulates the CysLT(1) receptor-mediated migration of endothelial cells; this may be regulated by the ERK1/2 pathway.

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Source
http://dx.doi.org/10.1254/jphs.08321fpDOI Listing

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