Bkaily Ghassan, Choufani Sanaa, Sader Sawsan, Jacques Danielle, d'Orléans-Juste Pedro, Nader Moni, Kurban Ghada, Kamal Maud
Department of Anatomy and Cell Biology, Faculty of Medicine, University of Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.
Can J Physiol Pharmacol. 2003 Jun;81(6):654-62. doi: 10.1139/y03-020.
The use of an ET-1 fluorescent probe in human heart and vascular smooth muscle cells showed that ET-1 receptors are present at both the sarcolemma and nuclear envelope membranes. The use of immunofluorescence studies showed that the ETA receptor was mainly present at the sarcolemma and cytosolic levels. However, the ETB receptor was present at the sarcolemma and the cytosol, as well as the nuclear envelope membranes and the nucleoplasm. In addition, ET-1 immunoreactivity was seen in the cytosol and the nucleus. Using Ca2+ fluorescent probes such as Fluo-3, Indo 1, and yellow cameleon, as well as confocal microscopy three-dimensional image measurement technique, stimulation of ET-1 receptors at the sarcolemma membranes induced an increase of cytosolic and nuclear free Ca2+ levels. This effect of extracellular ET-1 was blocked by removal of extracellular calcium. Direct stimulation of ET-1 receptors at the nuclear envelope membranes also induced an increase of intranuclear free Ca2+ level. Our results suggest that the stimulation of sarcolemmal Ca2+ influx by ET-1 seems to be due to the activation of ETA and ETB receptors. However, the increase of nucleoplasmic Ca2+ levels by cytosolic ET-1 seems to be mediated via the activation of ETB receptors. Activation of nuclear membranes ETB receptors seems to prevent nuclear Ca2+ overload and may protect the cell from apoptosis.
在人心脏和血管平滑肌细胞中使用内皮素-1(ET-1)荧光探针显示,ET-1受体存在于肌膜和核包膜膜上。免疫荧光研究表明,ETA受体主要存在于肌膜和胞质水平。然而,ETB受体存在于肌膜、胞质溶胶、核包膜膜和核质中。此外,在胞质溶胶和细胞核中可见ET-1免疫反应性。使用诸如Fluo-3、Indo 1和黄色变色龙等Ca2+荧光探针,以及共聚焦显微镜三维图像测量技术,刺激肌膜上的ET-1受体会导致胞质和核游离Ca2+水平升高。细胞外ET-1的这种作用可通过去除细胞外钙来阻断。直接刺激核包膜膜上的ET-1受体也会导致核内游离Ca2+水平升高。我们的结果表明,ET-1对肌膜Ca2+内流的刺激似乎是由于ETA和ETB受体的激活。然而,胞质ET-1导致核质Ca2+水平升高似乎是通过ETB受体的激活介导的。核膜ETB受体的激活似乎可防止核Ca2+过载,并可能保护细胞免于凋亡。