Ye Liyan, Guan Linbo, Fan Ping, Liu Yinghui, Xiong Wei, Liu Rui, Wei Xing, Zhu Yue, Liu Yu, Bai Huai
Laboratory of Genetic Disease and Perinatal Medicine and Key Laboratory of Birth Defects and Related Diseases of Women and Children of the Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, People's Republic of China.
Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, Sichuan, People's Republic of China.
Reprod Sci. 2019 Jun;26(6):745-756. doi: 10.1177/1933719118792102. Epub 2018 Aug 15.
Electrical stimulation induces significant angiogenesis in vivo. We have shown that electrical stimulation of trophoblast cells has important functions in aspects of angiogenesis. In this study, we investigated the effects of a direct current electrical field on trophoblast angiogenic tube formation. A 6-hour exposure to electric fields ranging from 50 to 150 mV/mm dose dependently increased tube growth and network formation. Additionally, the effect was time dependent, with increased tube formation occurring between 4 and 8 hours, indicating stimulation of trophoblast cell angiogenesis. Electrical fields of small physiological magnitude stimulated vascular endothelial growth factor expression by trophoblast cells in the culture. Electric field treatment also resulted in activation of Akt, while the activity of extracellular-regulated kinase 1/2, p38, and c-Jun NH2-terminal kinase was not significantly changed. Pretreatment with the vascular endothelial growth factor receptor (VEGFR)-2 inhibitor, SU1498, resulted in potent inhibition of tube growth, and the Akt inhibitor, MK-2206 2HCl, significantly reduced electric field-stimulated tubulogenesis. These data suggest the importance of the VEGFR-2 signaling pathway during electric field-induced trophoblastic angiogenesis. This novel evidence indicates that endogenous electrical fields may promote angiogenesis of trophoblast cells by stimulating the VEGFR signaling pathway.
电刺激在体内可诱导显著的血管生成。我们已经表明,对滋养层细胞进行电刺激在血管生成方面具有重要作用。在本研究中,我们研究了直流电场对滋养层血管生成管形成的影响。暴露于50至150 mV/mm的电场6小时,剂量依赖性地增加了管的生长和网络形成。此外,这种效应具有时间依赖性,在4至8小时之间管形成增加,表明滋养层细胞血管生成受到刺激。小生理强度的电场刺激培养中的滋养层细胞表达血管内皮生长因子。电场处理还导致Akt激活,而细胞外调节激酶1/2、p38和c-Jun NH2末端激酶的活性没有显著变化。用血管内皮生长因子受体(VEGFR)-2抑制剂SU1498预处理可有效抑制管的生长,而Akt抑制剂MK-2206 2HCl可显著降低电场刺激的管生成。这些数据表明VEGFR-2信号通路在电场诱导的滋养层血管生成过程中的重要性。这一新证据表明内源性电场可能通过刺激VEGFR信号通路促进滋养层细胞的血管生成。