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电刺激通过血管内皮生长因子(VEGF)受体发出信号,直接诱导血管内皮细胞产生促血管生成反应。

Electrical stimulation directly induces pre-angiogenic responses in vascular endothelial cells by signaling through VEGF receptors.

作者信息

Zhao Min, Bai Huai, Wang Entong, Forrester John V, McCaig Colin D

机构信息

Department of Biomedical Sciences, Institute of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, UK.

出版信息

J Cell Sci. 2004 Jan 26;117(Pt 3):397-405. doi: 10.1242/jcs.00868. Epub 2003 Dec 16.

Abstract

Controlling angiogenesis is crucial. Growth factors and cytokines are key regulators but a full understanding remains elusive. Endogenous electrical potential differences exist within and around the vasculature, both in relation to blood flow and in situations where active angiogenesis occurs, such as wound healing, development and tumor growth. Recent work shows that electrical stimulation induces significant angiogenesis in vivo, through enhanced vascular endothelial growth factor (VEGF) production by muscle cells. We report that applied electric fields (EFs) of small physiological magnitude directly stimulate VEGF production by endothelial cells in culture without the presence of any other cell type. EFs as low as 75-100 mV mm-1 (1.5-2.0 mV across an endothelial cell) directed the reorientation, elongation and migration of endothelial cells in culture. These pre-angiogenic responses required VEGF receptor activation and were mediated through PI3K-Akt and Rho-ROCK signaling pathways, resulting in reorganization of the actin cytoskeleton. This indicates that endogenous EFs might play a role in angiogenesis in vivo by stimulating the VEGF receptor signaling pathway, to induce key pre-angiogenic responses. In addition, it raises the feasibility of using applied EFs to initiate and guide angiogenesis through direct effects on endothelial cells.

摘要

控制血管生成至关重要。生长因子和细胞因子是关键调节因子,但全面了解仍很困难。血管系统内部及周围存在内源性电势差,这与血流以及诸如伤口愈合、发育和肿瘤生长等发生活跃血管生成的情况都有关系。最近的研究表明,电刺激可通过增强肌肉细胞产生血管内皮生长因子(VEGF),在体内诱导显著的血管生成。我们报告称,施加生理幅度较小的电场(EFs)可在无任何其他细胞类型存在的情况下,直接刺激培养中的内皮细胞产生VEGF。低至75 - 100 mV/mm-1(跨内皮细胞为1.5 - 2.0 mV)的EFs可引导培养中的内皮细胞重新定向、伸长和迁移。这些血管生成前反应需要VEGF受体激活,并通过PI3K - Akt和Rho - ROCK信号通路介导,导致肌动蛋白细胞骨架重组。这表明内源性EFs可能通过刺激VEGF受体信号通路,在体内血管生成中发挥作用,以诱导关键的血管生成前反应。此外,这也提高了利用施加的EFs通过直接作用于内皮细胞来启动和引导血管生成的可行性。

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