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乙醇通过蛋白激酶C(PKC)和丝裂原活化蛋白激酶(MAPK)介导内皮衍生细胞系EA hy926中的体外血管生成。

Induction of in vitro angiogenesis in the endothelial-derived cell line, EA hy926, by ethanol is mediated through PKC and MAPK.

作者信息

Jones M K, Sarfeh I J, Tarnawski A S

机构信息

Department of Medicine, Department of Veterans Affairs Medical Center, Long Beach, California 90822, USA.

出版信息

Biochem Biophys Res Commun. 1998 Aug 10;249(1):118-23. doi: 10.1006/bbrc.1998.9095.

Abstract

We have previously shown that ethanol-induced injury to the gastric mucosa triggers increased expression of the angiogenic factors, basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF) and angiogenesis. To further investigate ethanol-induced angiogenesis, we used an in vitro angiogenesis model which employs the ability of an endothelial-derived cell line (EA hy926) to form tubelike structures resembling capillaries when plated on the matrix material, Matrigel. We report that serum-starved EA hy926 cells, incubated for as little as 5 minutes with ethanol concentrations of 1.0-2.5%, formed tubelike structures reflecting in vitro angiogenesis. Control cells, not incubated with ethanol, did not form tubelike structures. Incubation for 5 minutes with 2.5% ethanol resulted in increased activities of PKC and MAP kinase (ERK2) by 1.6-fold (p < 0.05) and 2.3-fold (P < 0.001), respectively. Furthermore, inhibitors of the MAPK kinase, MEK (PD98059) and PKC (GF 109203X) prevented the induction of in vitro angiogenesis by ethanol.

摘要

我们之前已经表明,乙醇诱导的胃黏膜损伤会引发血管生成因子、碱性成纤维细胞生长因子(bFGF)和血管内皮生长因子(VEGF)表达增加以及血管生成。为了进一步研究乙醇诱导的血管生成,我们使用了一种体外血管生成模型,该模型利用内皮来源的细胞系(EA hy926)在铺于基质材料基质胶上时形成类似毛细血管的管状结构的能力。我们报告,血清饥饿的EA hy926细胞,用1.0 - 2.5%的乙醇孵育仅5分钟,就形成了反映体外血管生成的管状结构。未用乙醇孵育的对照细胞未形成管状结构。用2.5%乙醇孵育5分钟分别导致蛋白激酶C(PKC)和丝裂原活化蛋白激酶(ERK2)的活性增加1.6倍(p < 0.05)和2.3倍(P < 0.001)。此外,丝裂原活化蛋白激酶激酶(MEK,PD98059)和蛋白激酶C(GF 109203X)的抑制剂可阻止乙醇诱导的体外血管生成。

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