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Angiotensin II regulates endothelial cell migration through calcium influx via T-type calcium channel in human umbilical vein endothelial cells
Authors:A Martini  R Bruno  S Mazzulla  A Nocita  G Martino
Institution:1. Department of Cell Biology, Calabria University, Rende (CS), Italy

A. Martini and R. Bruno contributed equally to this work.;2. Department of Pharmaco-Biology, Calabria University, Rende (CS), Italy

A. Martini and R. Bruno contributed equally to this work.;3. Department of Cell Biology, Calabria University, Rende (CS), Italy

Abstract:Aim: The T-type calcium channel is expressed in vascular endothelial cells, but its role in endothelial cell function is yet to be elucidated. We analysed the endothelial functional role of T-type calcium channel-dependent calcium under angiotensin II (Ang II) stimulation. Methods: Human umbilical vein endothelial cells were co-incubated with hormone at 10?7 m and either Efonidipine 10?5 m or Verapamil 10?5 m or Mibefradil 10?5 m or Wortmannin 10?6 m . The contribution of Ang II receptors was evaluated using PD123319 10?7 m and ZD 7155 10?7 m . The calcium ion concentration was observed using Fluo-3 acetossimetil ester. The cells were observed after 3, 6, 9 and 12 h. Results: The microfluorescence method points out that Ang II induces intracellular calcium modulation in time by distinct mechanisms. AT2 receptor blockade is necessary to observe significant increase in Ca2+]i levels. Pre-treatment with Mibefradil abolishes Ang II -induced cell migration. Conclusions: Our data show that Ang II, via AT1 receptor, modulates calcium concentration involving T-type calcium channel and L-type calcium channel but only the calcium influx via T-type calcium channels regulates endothelial cell migration which is essential for angiogenesis.
Keywords:angiotensin II  HUVEC  mibefradil  verapamil  voltage-operated calcium channels
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