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亚阈值高频电场刺激诱导心肌细胞中血管内皮生长因子(VEGF)表达。

Subthreshold High-Frequency Electrical Field Stimulation Induces VEGF Expression in Cardiomyocytes.

作者信息

Rackauskas Gediminas, Saygili Erol, Rana Obaida R, Saygili Esra, Gemein Christopher, Laucevicius Aleksandras, Aidietis Audrius, Marinskis Germanas, Serpytis Pranas, Plisiene Jurgita, Pauza Dainius H, Schauerte Patrick

机构信息

Department of Cardiology, University Hospital, Aachen, Germany.

出版信息

Cell Transplant. 2015;24(8):1653-9. doi: 10.3727/096368914X682783. Epub 2014 Jul 8.

Abstract

Subthreshold electrical stimulation (SES) has been shown to induce an improvement of angiogenesis in ischemic and nonischemic skeletal muscles, mediated by increased VEGF expression. VEGF plays a key role in physiological and pathological angiogenesis. Cardiomyocytes possess the ability to synthesize and secrete VEGF. Thus, we thought to investigate the effect of SES on VEGF regulation in cultured neonatal rat ventricular myocytes (NRVMs), in the aim to reveal new techniques for therapeutic angiogenesis in ischemic heart disease. Cell cultures of NRVMs were electrically stimulated with field strengths below the myocyte depolarization threshold (0.5 V/cm with 1 ms bipolar impulse duration). Frequencies ranging from 5 Hz up to 25, 50, and 99 Hz were applied over a period of 48 h. The expression of VEGF and its receptor KDR was determined with Western blot and ELISA. To reveal the biological activity of the secreted VEGF amount, cultured human coronary artery endothelial cells (HCAECs) were treated with the cell culture supernatant of NRVMs exposed to SES. A dominant effect of SES was observed at 25 Hz. Within this particular frequency the VEGF protein amount in the cytoplasm as well as in the cell culture supernatant increased significantly. In parallel, the protein expression of the KDR receptor decreased in a significant manner. Moreover, cell culture supernatant of NRVMs exposed to SES augmented the growth of HCAECs. Cardiomyocytes respond to SES with an increase in biologically active VEGF expression that promotes cell proliferation of HCAECs. This mechanism may provide new approaches to develop therapeutic angiogenesis in the ischemic heart.

摘要

亚阈值电刺激(SES)已被证明可诱导缺血和非缺血骨骼肌血管生成改善,这一过程由血管内皮生长因子(VEGF)表达增加介导。VEGF在生理性和病理性血管生成中起关键作用。心肌细胞具有合成和分泌VEGF的能力。因此,我们试图研究SES对培养的新生大鼠心室肌细胞(NRVMs)中VEGF调节的影响,旨在揭示缺血性心脏病治疗性血管生成的新技术。用低于心肌细胞去极化阈值的场强(0.5V/cm,双相脉冲持续时间1ms)对NRVMs进行细胞培养电刺激。在48小时内施加5Hz至25Hz、50Hz和99Hz的频率。用蛋白质印迹法和酶联免疫吸附测定法测定VEGF及其受体KDR的表达。为了揭示分泌的VEGF量的生物学活性,用暴露于SES的NRVMs的细胞培养上清液处理培养的人冠状动脉内皮细胞(HCAECs)。在25Hz时观察到SES的显著作用。在这个特定频率下,细胞质以及细胞培养上清液中的VEGF蛋白量显著增加。同时,KDR受体的蛋白表达显著下降。此外,暴露于SES的NRVMs的细胞培养上清液促进了HCAECs的生长。心肌细胞对SES的反应是具有生物活性的VEGF表达增加,从而促进HCAECs的细胞增殖。这一机制可能为缺血性心脏病治疗性血管生成的发展提供新方法。

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